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Search Jobs by Category
| Miltenyi Biotec Inc. |
Northern California |
CA |
9/3/2010
|
| National Sales Manager - Instrumentation |
| Bachelor’s or graduate degree in the life sciences, and 5 years experience in equipment sales and management of sales personnel; or equivalent combination of education and experience required. Candidates must have strong track record in instrument / capital equipment sales.
We offer a competitive compensation and excellent benefits package. EOE/AA
To apply, go to: https://home.eease.adp.com/recruit/?id=521732 |
| Regeneron Pharmaceuticals, Inc. |
Tarrytown |
NY |
9/4/2010
|
| Research Associate- Therapeutic Antibodies |
| The ideal candidate should have BS degree in immunology, Biology, Biochemistry, or related discipline. Candidates with work experience in the area of immunization and monoclonal antibody development are most desirable. Minimum of 3-5 years laboratory experience is required. Knowledge of B cell development is a significant plus. Must be able to work productively in a fast-paced collaborative team environment. Excellent communication skills are essential.
|
| Regeneron Pharmaceuticals, Inc. |
Tarrytown |
NY |
9/4/2010
|
| Sr Flow Cytometry Specialist |
|
| Regeneron Pharmaceuticals, Inc. |
Tarrytown |
NY |
9/4/2010
|
| Medical Writer |
| *At minimum, a Bachelor's degree (BS) from an accredited college or university, and 6 years of medical writing experience (CSR's, CSP's, IB, and Clinical Summaries).
*Experience leading NDA/BLA filings and some management experience.
*EMEA filing experience a plus.
*Strong knowledge of the clinical research process and regulations/guidelines required.
*Must have strong organizational, interpersonal, leadership, and communication skills.
*Must be able to communicate effectively in large or small group settings.
*Effective influence and relationship management skills required.
*Working knowledge of one or more EDM systems.
|
| Regeneron Pharmaceuticals, Inc. |
Tarrytown |
NY |
9/4/2010
|
| Scientist- Assay Development |
| Ph.D. in Biology, Immunology or a related field
-2-5 years of industry or laboratory experience
-Experience developing ELISAs and cell-based assays
-Experience in the validation of ELISAs and cell based assays for protein biopharmaceuticals in a regulated environment under GLPs is required.
-The successful candidate must possess excellent organizational and communication skills
-Must be able to maintain lab notebook and keep a safe lab environment
-The ability to effectively interact with colleagues in a team environment
-Ability to independently plan, supervise and direct projects to completion are essential
|
| Regeneron Pharmaceuticals, Inc. |
|
|
9/4/2010
|
| Research Associate- Protein Sciences |
| Requirements:
- B.S or MS or equivalent in biochemistry
- 0-3 years post-graduate experiences in protein biochemistry
- Knowledge in LC/MS for protein and peptide analysis
- Strong organization and communication skills and effective interpersonal skills
- Ability to learn new technologies and solve problems
- Ability to work in a team environment
|
| Regeneron Pharmaceuticals, Inc. |
|
|
9/4/2010
|
| Process Development Engineer |
| The ideal candidate will have a Bachelors or Masters degree in Chemical Engineering with a concentration in biochemistry and 0 - 5 years experience in the biotech or pharmaceutical industry. Knowledge and experience with bioseparations processes is preferred.
|
| Regeneron Pharmaceuticals, Inc. |
Tarrytown |
NY |
9/4/2010
|
| Research Associate II - Bispecifics |
| The qualified individual will possess a Bachelor's degree in Biology or related medical science with 1-3 years laboratory experience or a Master's degree and 0-1 years experience. Must be able to work productively in a fast-paced collaborative team environment. The candidate should have experience in protein expression vector construction and analysis as well as in conducting cell based assays. Experience with ELISA assays is also a plus. Excellent communication skills are essential. Candidate should be proficient in Microsoft Office and statistical analysis programs. A background in immunology or oncology is highly desirable. |
| Regeneron Pharmaceuticals, Inc. |
|
|
9/4/2010
|
| Regulatory Associate IV |
| Requires a MD or PhD and a minimum of 5 years of pharmaceutical industry experience. Research laboratory, process development or manufacturing experience with biotechnology products is highly desirable.
*Advanced knowledge of 21 CFR Parts 50, 54, 56, 58, 210, 211, 312, 314, 600, 601, and monitors newly published FDA guidelines and international guidance documents in the context of new and ongoing development programs. Negotiation and communication skills a must.
|
| Regeneron Pharmaceuticals, Inc. |
Tarrytown |
NY |
9/4/2010
|
| Senior Buyer- Indirect Services |
| 'Bachelor's or Master's degree or equivalent work experience required; C.P.M. or C.P.M.S. required
'5-8 years progressive experience in Procurement with an emphasis on Information Technology and Facilities
'Experience working in/with Pharma/Biotech companies required (mid-sized Biotech strongly preferred)
'Robust project management support for multiple projects to ensure the successful completion of specific project goals and objectives are met within budget and on time, i.e. IT projects, new building requirements
'Demonstrated ability to drive results in an expedient manner quickly gathering information and consensus along with making sound decisions
'Translates business objectives into actionable priorities
'Ability to perform with minimal supervision
'Demonstrated ability to support internal clients and lead
'Competent in effectively communicating, both verbally and in writing within all levels of the organization
'Demonstrated ability to think and act strategically
'Proven experience in negotiating, reviewing and managing client requirements; contracts; policies and procedures
'Extensive experience in negotiating agreements for the organization, i.e. Contract/Pricing Agreements such as waste management; uniforms
'Vendor/Partner relationship management
'Demonstrated ability to work well with people from many different disciplines
'Oracle or similar ERP solution experience preferred
'Expert in the use of Microsoft Office suite (Word, Excel, Power Point,Visio) and MS Outlook
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| Regeneron Pharmaceuticals, Inc. |
Tarrytown |
NY |
9/4/2010
|
| Scientist/Post Doctoral Genome Engineering |
| Technical Skills: Experience with analyzing phenotypes in mutant mice. Experience with genotyping and gene expression analysis techniques. Microscopy techniques. Also experience with ES cells and/or iPS cells. Previous experience as supervisor not required but will also be considered an advantage.
|
| New England Biolabs, Inc. (NEB) |
Ipswich |
MA |
9/4/2010
|
| Associate Director of Business Development |
| •Generate revenue opportunities through new ventures, partnerships and strategic alliances.
•Support NEB’s existing program for analysis of technologies, including identification of potential markets.
•Identify and establish collaborative working relationships throughout NEB; actively soliciting input and support for business development initiatives.
The ideal candidate will have:
•experience in strategic partnering, licensing of IP and technologies, and the development of OEM business.
•strong project management skills coupled with the ability to multi-task, prioritize and manage multiple projects simultaneously.
•a strong scientific orientation, demonstrating an in-depth knowledge of molecular biology reagents and technologies.
•demonstrated proficiency in identifying and communicating the appropriate level of scientific and business information about reagents and technologies to customers, collaborators and business partners.
Qualifications:
•Minimum of Ph.D. in Life Sciences with a strong background in molecular biology, or related field.
•Minimum of 5 years experience in a business development or licensing setting.
•Be available for domestic and international travel approximately 30% of time.
New England Biolabs, Inc. is an equal opportunity employer M/F/D/V
|
| Morphotek®, Inc. |
Exton |
PA |
9/4/2010
|
| Sr. Manager/Manager of Project Planning and Informatics |
| Knowledge/Skills/Abilities Required
• Bachelors degree with a minimum of 5 years relevant work experience (Manager) or 8 years of relevant work experience (Sr. Manager)
• At least 3 years experience in Clinical Project Management role, Clinical Informatics role or equivalent position
• Very strong systems / informatics background required
• Very strong organizational and analytical skills required
• MS Project experience strongly preferred |
| Morphotek®, Inc. |
Exton |
PA |
9/4/2010
|
| Senior Scientist, Fermentation |
| Knowledge/Skills/Abilities Required
• PhD trained in biochemical engineering sciences or related scientific discipline with minimum of three years of post-doctoral experience in the field of bioreactor fermentation, preferably in an industrial setting
• Extensive hands-on experience in mammalian cell culture process; in-depth working knowledge of stainless steel and disposable fermentors (2L to 250L);
• Must be able to lift at least 50 lbs
• Supervisory skills required
• Good verbal and written communication skills required
• Good interpersonal skills with the ability to work in a team environment required |
| Teva Pharmaceuticals USA |
Forest |
VA |
9/4/2010
|
| Manufacturing Supervisor - 3rd Shift |
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| Teva Pharmaceuticals USA |
Saint Joseph |
MO |
9/4/2010
|
| Chemist II - Chemistry |
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| Teva Pharmaceuticals USA |
Irvine |
CA |
9/4/2010
|
| Director, Maintenance |
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| Teva Pharmaceuticals USA |
Irvine |
CA |
9/4/2010
|
| System Administrator/Business Analyst II IT |
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| Teva Pharmaceuticals USA |
Irvine |
CA |
9/4/2010
|
| Sr. Regulatory Compliance Auditor |
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| Teva Pharmaceuticals USA |
Irvine |
CA |
9/4/2010
|
| Metrologist/Sr. Metrologist |
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| Teva Pharmaceuticals USA |
Irvine |
CA |
9/4/2010
|
| Sr. Supervisor/Supervisor Microbiology (2nd Shift) |
|
| Teva Pharmaceuticals USA |
Irvine |
CA |
9/4/2010
|
| Principal Scientist I - Preformulation/Formulation Group Leader |
|
| Teva Pharmaceuticals USA |
Irvine |
CA |
9/4/2010
|
| Validation Engineer I |
|
| Agilent Technologies, Inc. US |
Folsom |
CA |
9/4/2010
|
| Manufacturing Technician |
| The successful candidate will possess the following:
- Experience working in a manufacturing environment. Chemical experience preferred.
- Ability to work with small volumes of chemicals and fine chemical manufacturing and/or laboratory environment
- Demonstrate effective verbal and written communication skills
- Aptitude to follow complex instructions
- Capability to adapt to changing priorities
- Able to multi-task and organize thoughts as needed
- Willingness to lead and motivate others
- Ability to work independently and within a team
- Able to establish and maintain positive work relationships
- Willingness to work overtime as required
- Competence in planning and organizing workload
- Ability to follow verbal and written instructions
- Strong attention to detail
- Fine motor skills and ability to see and work with small objects
Geo Location: Folsom, CA |
| Agilent Technologies, Inc. US |
Chandler |
AZ |
9/4/2010
|
| Sales - Genomics Product Specialist |
| - Minimum BS/MS in Chemistry or a Life Sciences discipline, or equivalent.
- Solid self management and organizational and prioritization skills
- 5+ years related direct sales experience with a demonstrated track record of successfully selling against a quota.
- High level of experience in microarrays and/or NGS.
- Technical knowledge and domain knowledge in the research and diagnostic sector of the pharmaceutical industry (profit and not for profit. Knowledge of the cytogenetics market.
- Industry/Application expertise. Working knowledge of competitive products (specifications, value propositions, price points).
- Comfortable interfacing with senior managers within your customers.
- Demonstrated commercial selling skills. Strong business development and sales closing skills.
- Effective interpersonal communication and telephone sales skills.
- Must be able to travel up to 35% of the time.
Geo Location: Arizona (preferred) or Texas |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Senior Software Engineer |
| * Bachelors or Masters degree in computer science and/or physical science.
* More than 5 years experience in industry-related software development
* Experience in the following software fields
- Application development experience using Oracle and SQL databases and Schema Design
- Windows development using .NET, C#, and C++
- Experience with Windows Services, WCF, Web Services
- Experience in server side development
- Desired experience in MVVM & CAL, MSI, MSBuild and WIX
- Also desired are experiences in Search Technologies, Data Object Design and Data Warehousing |
| Agilent Technologies, Inc. US |
Boulder |
CO |
9/4/2010
|
| Manufacturing Chemist |
| Requires:
? BS in chemistry, biology, biochemistry, science or equivalent
? 5+ years of related experience in a lab or manufacturing environment preferably within a pharmaceutical environment
? Previous knowledge of oligonucleotide Synthesis, HPLC, UF and Lyophilization a plus.
? Detail oriented and can perform technical duties following standard operating procedures and general laboratory safety rules.
? Ability to work both independently and in a team setting on a variety of projects and use individual discretion to meet required project objectives and deadlines.
? Excellent math, documentation, communication and operational trouble shooting skills.
? Ability to work as a successful member of a team working to establish priorities and procedures to collectively to meet department goals and project deadlines.
? Ability to work in a clean room environment.
? Previous experience in a FDA regulated manufacturing environment highly desired |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Marketing Director - Life Sciences |
| Requires:
- BS in biology, biochemistry, molecular biology; related discipline or equivalent. Master or PhD preferred.
- 8+ years experience in marketing life science products.
- Demonstrated use of marketing skills and market knowledge to define and commercialize products that result in business success
- Experience in working with worldwide customers and is a strong advocate for customer focus and customer driven development
- Demonstrate ability to develop marketing plans that align with strategic objectives
- Ability to work independently to plan, prioritize workload, schedule time, assess and solve problems
- High proficiency in pricing and forecasting
- Must exhibit strategic thinking, teamwork, creativity, planning and organization, and flexibility
- Strong analytical and decision making skills
- Experience in working with global markets/customers an advantage
- Excellent written and oral communications skills and comfortable presenting to high level audiences both internally and externally
- Must have flexibility in working hours and available for 25% business travel
Geographic Location: Santa Clara, California |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Clinical Program Marketing Manager |
| Qualifications:
Scientific Credentials: Scientific Degree in Analytical Chemistry, Clinical Chemistry or similar field. PhD preferred.
Relevant Work Experience: 5+ years experience in a clinical testing laboratory, clinical industry and/or previous sales/marketing position in an analytical instrumentation business
Clinical Domain Expertise: Fluent in all aspects of clinical chemistry lab operations. Working knowledge of sample prep, chromatography and quantitative LC/MS is required.
Communication Skills: Excellent written, verbal, and presentation skills essential.
Teamwork: Ability to function effectively in a matrix structure. Track record of success driving cooperation among global cross-functional teams. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Software Engineer |
| Job Requirements:
? Strong C# programming experience.
? Experience using Microsoft Visual Studio and source management tools, such as Microsoft Team Foundation Server.
? Experience using DevExpress, WPF, or similar GUI toolset.
? Broad knowledge and experience using design patterns.
? Strong work ethic with focus on quality, follow-through, and attention to detail.
? Good communication skills.
? Experience synthesizing a cohesive system consisting of hardware, electronics, firmware, and software.
Education & Experience:
? Degree in computer science, engineering, or related field.
? 5+ years of technical experience.
? Experience developing production quality software.
? Experience with C++ desired.
? Experience with TCP/IP desired.
? Experience with embedded programming desired. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Pharma LC/MS Application Champion |
| Bachelors or Master Degree or University Degree or equivalent. PhD is preferred. A minimum of 5 years relevant experience, with typically 9 to 15 years practical experience.
The successful person for this position will:
Be comfortable with LC/MS analysis of pharmaceutical compounds.
Have the ability to use new LC/MS technology especially TOF and triple quadrupole based technology.
Have familiarity with software tools to assist in data processing for the production of proof statements and application notes
Have a good understanding of pharmaceutical MS analysis including DMPK, ADME and metabolite identification.
Be an effective communicator , have good written English skills and be an effective team player
Ability to lead and design the workload of other application personnel
Geo Location: Santa Clara, CA |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Clinical LC/MS Applications Champion |
| BS or PhD Degree (preferred) or equivalent in Chemistry, BioChemistry, Biology, or related field.
Minimum of 5 years relevant experience with typically 9-15 years practical experience.
The successful person for this position will:
Be comfortable with LC/MS analysis of peptides, steroids, amino acids, vitamins : sample preparation, instrument operation, data analysis, and data interpretation and processing.
Have the ability to use new LC/MS technology especially TOF and triple quadrupole technology.
Have familiarity with software tools to assist in data processing for the production of proof statements and application notes.
Have a good understanding of clinical MS analysis
Be an effective communicator , have good written English skills and be an effective team player.
Ability to lead and design the workload of other application personnel.
Geo Location: Santa Clara, CA |
| Agilent Technologies, Inc. US |
San Francisco |
CA |
9/4/2010
|
| LCMS Applications Scientist - Clinical |
| - PhD in Chemistry or Biology or Biochemistry or equivalent
- 5+ years hands-on experience in the field of Mass Spectrometry in a clinical setting
- Experience with a broad range of LCMS instrumentation
- Experience in a clinical setting required
- Excellent verbal, written and presentation communications skills
- Strong project management experience skills
- Available for flexible work schedule and business up to 50% business travel.
Agilent will not sponsor work authorization |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Electrical Engineering Coop |
| Must have:
1) Minimum Qualifications· pursuing MS in Computer Science, Computer Engineering, or EECS, MS degree EE or equivalent
2) Understanding of operating systems and software drivers
3) Basic understanding of hardware
4) Experience programming with one of more of the following: Linux, BSO, Windows, VxWorks
5) Strong data analysis skills.· Excellent communication skills.· Ability to function effectively in a team environment.· Ability to quickly learn new technologies
6) Experience with object oriented languages. C++ Java.
7) Experience with C and Visual Basic
8) Real-hands on training in Software development
9) - Experience with high performance RTL and associated verification and debug
- Experience with PCB physical mixed-signal design tools and flows
10) - Mix-signal (Analog and Digital) circuits
- Strong communication and teamwork skills
11) - Embedded uProcessor knowledge
Must be able to work for at least 6 months on a full time basis. Students who can not do this will not be eligible. Must be able to start in Dec/Jan 2011. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Electrical Engineering Coop |
| Must have:
1) Minimum Qualifications· pursuing MS in Computer Science, Computer Engineering, or EECS, MS degree EE or equivalent
2) Understanding of operating systems and software drivers
3) Basic understanding of hardware
4) Experience programming with one of more of the following: Linux, BSO, Windows, VxWorks
5) Strong data analysis skills.· Excellent communication skills.· Ability to function effectively in a team environment.· Ability to quickly learn new technologies
6) Experience with object oriented languages. C++ Java.
7) Experience with C and Visual Basic
8) Real-hands on training in Software development
9) - Experience with high performance RTL and associated verification and debug
- Experience with PCB physical mixed-signal design tools and flows
10) - Mix-signal (Analog and Digital) circuits
- Strong communication and teamwork skills
11) - Embedded uProcessor knowledge
Must be able to work for at least 6 months on a full time basis. Students who can not do this will not be eligible. Must be able to start in Dec/Jan 2011. |
| Agilent Technologies, Inc. US |
Chandler |
AZ |
9/4/2010
|
| Product Marketing Engineer |
| - Bachelor degree in relevant science or engineering discipline; Ph.D. strongly preferred (e.g. Material Science, Life Sciences, Chemistry, Physics, Biology or Biophysics)
- 5+ years recent experience applying scanning electron microscopy to scientific, industrial and/or manufacturing problems; understanding of electron-specimen interactions
- Exceptional written and verbal communication skills; Ability to address a diverse audience is critical to the successful candidate
- Versatile interpersonal skills to communicate across geographies, cultures, organizational functions.
- Domestic and international travel required
- Ability to speak a second language highly desirable
Geo Location: Chandler, AZ |
| Agilent Technologies, Inc. US |
Anaheim |
CA |
9/4/2010
|
| Field Service Engineer- Los Angeles Area |
| Requires BS or MS Degree or equivalent and 3 or more year's relevant experience with the use,repair,troubleshooting of hardware, software applications support and routine preventative maintenance, qualification and verification of Agilent's Liquid Chromatographs and LC Mass Spectrometers. LCMS experience required.
Geographic Location: Los Angeles Area
Agilent will not sponsor work authorization for this position |
| Agilent Technologies, Inc. US |
Columbia |
MD |
9/4/2010
|
| Wireless Network Engineer - Application Support |
| ?Bachelors or Masters Degree in Electrical/Electronic or Computer Engineering and 5+ years applicable experience in Mobile Communication Systems and Networks (including cell phone and other mobile communications infrastructure).
?Knowledge of wireless protocols, including: UMTS, GPRS, GSM and CDMA technologies
?Strong Linux/Unix system administration experience.
?Experience with Central Office networking
?Experience with Perl and Shell Scripting
?Experience with end user, installation and commissioning of new systems within customer environments is highly desired.
?Knowledge of Network Signaling is preferred
?Strong interpersonal/relationship skills, solid written and verbal communications.
?US citizenship is required, based on customer requirements
?Current high level US Government Security Clearance -or- ability to process for and obtain high level US Government Security Clearance.
Position is in Columbia, Maryland area. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| R&D Bioinformatics, Senior Software Engineer |
| External Qualifications:
This dynamic position requires a MS degree in Computer Science or equivalent plus a minimum of 5+ years relevant experience with bioinformatics tools and procedures as applied to high-throughput computational pipelines.
Chosen candidate must have the following:
? 5+ years experience in C++, .NET, and Java
? Object oriented programming experience a plus
? Experience with: BLAST, BLAT and/or MOST
? Experience with SQL and/or Oracle database
? Knowledge of public biological databases, tools, and repositories is required
? Hands-on experience producing software in collaborative, multidisciplinary environment to solve problems in biological or other life science is highly desirable
? Experience with Image Analysis is a plus
Geographic Location: Bay Area, California (Santa Clara) |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| R&D Bioinformatics, Software Engineer |
| External Qualifications:
This dynamic position requires a MS degree in Computer Science or equivalent plus a minimum of 5+ years relevant experience with bioinformatics tools and procedures as applied to high-throughput computational pipelines.
Chosen candidate must have the following:
? 2+ years of experience in providing bioinformatics solution in next gen sequencing space.
? 5+ years experience in C++, .NET, and Java
? Object oriented programming experience a plus
? Experience with: BLAST, BLAT and/or MOST
? Experience with SQL and/or Oracle database
? Knowledge of public biological databases, tools, and repositories is required
? Hands-on experience producing software in collaborative, multidisciplinary environment to solve problems in biological or other life science is highly desirable
? Experience with Image Analysis is a plus
Geographic Location: Bay Area, California (Santa Clara) |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Product Manager |
| Educated to at least university degree level or equivalent, you'll bring at least 9 years' practical experience, through which you'll developed an in-depth knowledge of market and channel distribution mechanisms. This is where your specialist knowledge, technical leadership and customer-focused, solutions-oriented approach will thrive.
Geo Location: Santa Clara, CA |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| RF Field Applications Engineer |
| Position requires Bachelors or Master Degree or equivalent and a minimum of 2-4yrs+ in an Applications Engineering or Sales Support role.
? Must be US citizen.
? Must have knowledge of RF and microwave products such as network analyzers, signal generators and spectrum analyzers.
? Candidate must be knowledgeable of competition and able to identify lockout specification (identify Agilent's competitive advantage over competition)
? Must be able to analyze customer requirements and recommend appropriate solutions
? Must possess excellent communication skills |
| Agilent Technologies, Inc. US |
Budd Lake |
NJ |
9/4/2010
|
| Field Service Engineer (Electronics) |
| Minimum education, training and experience needed to perform this job:
1. Typically requires two (2) years of electronics related college education plus six (6) years of related experience, or an equivalent combination of technical training and related experience.
2. Strong understanding of electronic circuitry including current state-of-the-art devices as well as ability to effectively troubleshoot the most complex
systems.
3. Prior field service experience.
4. NMR experience a plus.
Territory: NJ, PA
Geo Location: Newark or Philadelphia |
| Agilent Technologies, Inc. US |
Budd Lake |
NJ |
9/4/2010
|
| Field Support Specialist (Chemist) |
| Minimum education, training and experience needed to perform this job:
1. BS degree in chemistry or bio-chemistry plus five years of related experience; or an equivalent combination of education and related experience.
2. Strong understanding of electronic circuitry including current state-of-the-art devices as well as ability to effectively troubleshoot complex systems.
3. Prior NMR applications experience a must.
Territory: NJ, PA
Geo Location: Newark or Philadelphia |
| Agilent Technologies, Inc. US |
Ft. Lauderdale |
FL |
9/4/2010
|
| On-Site Field Service Engineer |
| University Degree or equivalent plus a minimum of 8+ years relevant experience, with typically 10+ years practical experience with Electronic Measurement Equipment.
Position requires:
? 8+ years directly related experience as Field Service Engineer calibrating and repairing Electronic Measurement Equipment.
? Expert skills in the calibration and repair of all types of Agilent and Multivendor Test Equipment
? Experience using automated calibration software platforms (STE, PC Based, etc) is required
? Must have proven leadership skills as a Team Lead/Mentor
? Strong Customer interface skills
This position is based in Plantation, Fl ( North of Miami). Candidates must be local or willing to relocate themselves. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Sr.Engineer/Ass. Staff Engineer |
| B.S. degree in physics, chemistry, or electrical engineering or equivalent, plus a minimum of 7 years of related experience, or an equivalent combination of M.S or Ph.D. degree and experience. Advanced degree and minimum of 6 years of relevant experience required for Staff Engineer.
*NMR experience, NMR systems experience and good operating knowledge of VNMRJ are strongly preferred.
*Good RF, analog, and digital electronic experience and operation of related test equipment required. And/or experience with High Powered RF preferred
*Mechanical engineering and machine shop experience a plus.
*Unix/Linux operating knowledge, basic CAD experience, and knowledge of MS Office required.
Strong analytical and troubleshooting skills are required.
*Good verbal and written communications skills. |
| Agilent Technologies, Inc. US |
Chicago |
IL |
9/4/2010
|
| Field Support Specialist (Chemist) |
| Minimum education, training and experience needed to perform this job:
1. BS degree in chemistry or bio-chemistry plus five years of related experience; or an equivalent combination of education and related experience.
2. Strong understanding of electronic circuitry including current state-of-the-art devices as well as ability to effectively troubleshoot complex systems.
3. Prior NMR applications experience a must.
Territory: Midwest
Geo Location: Chicago or Indianapolis |
| Agilent Technologies, Inc. US |
Boulder |
CO |
9/4/2010
|
| Supply Chain Manager |
| Key qualifications and/or experience for the position.
Education:
Advanced degree in Chemistry or MBA (emphasis in supply chain management preferred)
Experience:
Minimum of 10 years strategic sourcing experience in pharmaceutical or specialty chemical manufacturing
Demonstrated ability to develop strategic sourcing plans
Contracts preparation and management experience
Inventory management experience
International experience in logistics, transportation and distribution of raw materials
Functional expertise with Supply Chain Management systems
Professional Skills:
Strong interpersonal skills, strong organizational skills, and ability to analyze complex data
Project management or client/supplier relationship management experience
Ability to work effectively in an interdisciplinary and cross functional team environment
Analytical chemistry knowledge with the ability to set, justify and negotiate specification
In depth understanding of the connection between raw material quality, specifications and final product quality
Leadership Skills
The successful candidate will have a demonstrated ability to affect change in high growth business environment and motivate direct and indirect assets to achieve challenging goals.
Computer Skills
Proficiency in the use of MS office applications and relational data base management
Understanding of SAP, Oracle, MRP or other financial/inventory management systems |
| Agilent Technologies, Inc. US |
Loveland |
CO |
9/4/2010
|
| Software Application Engineer |
| Job requirements: This is a key role within an advanced development team. The position requires the following:
? Bachelors or Masters degree in Computer Science or equivalent experience
? Must have at least 4 years technical expertise in SW development processes throughout the development lifecycle (concept to product release)
? Embedded OS & real-time operating systems - WinCE, embedded Linux
? Leadership skills to effectively drive change within R&D teams
? Iterative development techniques - scrum, XP, etc.
? Languages including C++, C#, & Python
? Strong written and verbal communication skills
? Strong collaboration skills with multiple cultures around the world.
Relocation benefits are available |
| Agilent Technologies, Inc. US |
Wilmington |
DE |
9/4/2010
|
| Sr. Manager of Global Marketing - Chemistries |
| Qualifications:
- Bachelor Degree in Business or Sciences or equivalent, MBA preferred.
- 5+ year progressive global marketing management experience including comprehensive experience in benchmarking, market research, advertising, promotions, forecasting and pricing
- Demonstrated ability effectively launching new products and achieving excellent business results.
- Proven success integrating resources across complex functions (sales, marketing, R & D, Supply chain) and across multiple geographies to over-deliver on customer needs. |
| Agilent Technologies, Inc. US |
Columbia |
MD |
9/4/2010
|
| Program Manager |
| ? Bachelors or Masters Degree in Electrical Engineering or Computer Science or equivalent experience.
? Ten or more years experiance in the industry with five or more years as a Program/Project Manager
? Background in Wireless or IP networking preferred.
? Experience executing DoD programs throughout a milestone-oriented program life cycle.
? Track record of delivering quality solutions on time and delighting customers
? Mastery of Microsoft Project, Excel, Word, and Outlook
? Experience in new product, or novel system, development processes (e.g., software or hardware) as well as experience with life cycle support processes.
? Proven ability to work in a team, gain alignment among customers, teams, peers, partners, and management
? Proven ability to adapt to changing requirements in response to pressing customer needs
? Proven ability to prioritize and balance resources across multiple projects
? Experience with leading, planning, organizing, tracking and reporting for project teams and tasks
? Meticulously attentive to detail
? Experience with mentoring, staffing, and people development.
? PM Certification a plus, but not required. (Experience counts for more.)
? US Citizen with, or capable of obtaining, a high level security clearance. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| R&D Production Manager |
| This is a managerial position for NMR Cold Probe Production and NPI. The manager is responsible for overseeing the assembly and test of all production cold probes, and coordinating closely with development on specials. The manager will also be responsible for working closely with Cold Probe Development on the smooth introduction of new products into production.
List Minimum education, training and experience needed to perform this job:
1. 15 years experience with NMR probes
2. 5 years minimum supervisory experience
3. familiarity with cryogenic and vacuum systems
4. 10 years manufacturing/production engineer experience |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Senior Global Buyer |
| List Minimum education, training and experience needed to perform this job:
1. Minimum 4-year degree required (or equivalent)
2. Proficiency in ERP/e-procurement systems required. (Will train in ERP systems for right candidate.)
3. 3-5 years experience in procurement industry, supply chain management (SCM) required (for new college graduate ? courses or focus in Procurement / SCM required)
4. Strong interpersonal and teamwork skills
5. Able to make decisions based on quantitative data required |
| Agilent Technologies, Inc. US |
Santa Rosa |
CA |
9/4/2010
|
| R&D FPGA Engineer |
| Key required skills:
? Bachelors or Masters Degree or University Degree in Electrical Engineering and 5+ years applicable experience in FPGA design
? Ability to use FPGA simulation and design tools to realize and verify high quality and robust solutions in Verilog or VHDL.
? Experience with Xilinx ISE, including Plan Ahead, and synthesis tools, such as Synplify
? Ability to perform characterization and testing of design prototypes, and analyze and validate the design to meet product performance specifications.
? Strong interpersonal/relationship skills, solid written and verbal communication skills
Desired skills:
? Educational emphasis or work experience with signal processing theory, applications and development
? Skills in signal processing algorithm development and implementation using FPGAs
? Experience with team-based FPGA development ? design partitioning and integration
? Knowledge in high-speed digital design, PCI Express, DMA, memory systems |
| Agilent Technologies, Inc. US |
Everett |
WA |
9/4/2010
|
| R&D Signal Processing Software Engineer |
| Key Required Skills:
? Bachelors or Masters Degree or University Degree in Electrical Engineering or Computer Science
? Must have 5+ years applicable experience in software development involving signal processing theory, techniques and algorithm development
? Must have experience with the use of computer tools for simulation
? Must have demonstrated proficiency with C/C++ or C# programming languages
? Strong interpersonal/relationship skills, solid written and verbal communication skills
Additional Desired Skills:
? Proficiency with C#,.Net, Visual Studio, defect tracking, revision control, real-time systems and software/firmware lifecycles. |
| Agilent Technologies, Inc. US |
Everett |
WA |
9/4/2010
|
| R&D Hardware Control Software Engineer |
| This is a key SW development role.
Key Required Skills:
? Bachelors or Masters Degree in Electrical Engineering or Computer Science
? 3+ years applicable experience in software development involving hardware control and IO
? Must have proficiency with C#, C++, .Net, Visual Studio, defect tracking, revision control and software/firmware lifecycles
? Strong interpersonal/relationship skills, solid written and verbal communication skills
Additional Desired Skills:
? Familiarity with Windows device drivers
? Experience with the Windows Presentation Foundation graphical subsystem
? Educational emphasis or work experience with signal processing theory, applications and development |
| Agilent Technologies, Inc. US |
Santa Rosa |
CA |
9/4/2010
|
| Manufacturing Engineer |
| B.S. or M.S. in Chemistry, Chemical Engineering, Materials Science, Physics or equivalent experience.
Analytical Chemistry experience is essential and electroplating, chemical milling and/or materials science experience is highly desirable.
Experience with statistical process control and design of experiments is desired.
Candidates should have excellent interpersonal, problem solving, and communication skills.
US Citizenship/Permanent Resident status is highly recommended, but applications from highly qualified candidates requiring work sponsorship will also be considered.
Candidates requiring work sponsorship must be eligible for access to export controlled technology. |
| Agilent Technologies, Inc. US |
Newport |
DE |
9/4/2010
|
| Manufacturing Operations Coordinator |
| Musts:
- Demonstrated ability to work in a team environment.
- Demonstrated strong communication and organizational skills.
- Demonstrated ability to read and understand written procedures and instructions.
- Demonstrated ability to perform basic math (add, subtract, multiply, divide, ratios, weights & measures).
- Demonstrated ability to make timely decisions.
- Experience with troubleshooting and applying corrective actions.
- Demonstrated ability to maintain accurate records.
- Experience working with computers: keyboarding, Windows environment.
- Demonstrated ability to manipulate small parts, manual dexterity.
- Required to bend, stoop, and reach.
- Required to remain standing for extended periods of time.
- No known allergies to chemicals used in the work area.
- May be required to lift materials per entity specified and approved limits.
- May be required to participate in medical/screening or monitoring programs.
Desired:
- Basic PC skills: spreadsheets, word processing, databases.
- Previous manufacturing experience in an ISO certified environment. |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
9/4/2010
|
| Manufacturing Engineer |
| Minimum of 4 years relevant experience, with typically 5 to 8 years.
BSEE or higher degree
Basic circuit theory and analysis
Analog RF measurement and analysis using network analyzers and s-parameters
Proven ability to analyze and debug circuits at the component level
Extensive programming background in an in-line language such as Pascal or C
(Want) National Instruments Labview programming experience
Behavioral:
Ability to work with other people in stressful situations
Ability to investigate and troubleshoot complex problems
Ability to prioritize work when there are many different tasks to be done
Ability to learn new tools and equipment quickly and independently |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
9/4/2010
|
| Manufacturing Technician |
| You must have extensive experience with thick film screen printing or semiconductor photolithography/etch. 2 year-degree with minimum 7 years experience, 9?15 years preferred |
| Agilent Technologies, Inc. US |
Santa Rosa |
CA |
9/4/2010
|
| IC Product Engineer |
| M.S. or Ph.D. in Electrical Engineering, Materials Science or equivalent experience. Experience with advanced III-V semiconductor device fabrication, characterization and reliability is essential. Specific experience in high speed/frequency GaAs, InP and GaN device physics and RF microwave engineering is highly desirable. Experience with statistical process control and design of experiments is required. Candidates should have excellent interpersonal and communication skills for successful inter-group and intra-group interactions. This engineer must be highly motivated in order to accomplish all the tasks required to meet very aggressive product development schedules and world class manufacturing expectations.
Agilent will not sponsor work authorization for this position |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| GC/MS General Manager |
| COMPETENCIES REQUIRED
? General Management and proven Leadership Skills in a Complex, Global Environment. The GM will have demonstrated his/her ability to lead an organization by setting and meeting goals and motivating performance, despite obstacles and setbacks. Experience in coordinating, motivating and leading a multifunctional, dispersed team within a global large organization is essential. Expertise in creating compelling business plans and presentations for internal and external audiences is required. Similarly, it is essential this individual have good financial management skill and an ability to work closely with finance professionals in preparing strategic business plans.
? Relevant Industry/Scientific Understanding. This individual will have demonstrated current understanding and working knowledge of analytical instrumentation tools for the Chemical Analysis laboratories.
? Customer Relationship Orientation. S/he will have demonstrated insight into customers, their businesses, needs and values. Commitment to customers and building strong, long-term customer relationships will be of critical importance. An ability to leverage existing distribution channels, and to establish strategic partnership with the sales and marketing team will be key.
? Open and Effective Communicator with Strong People Skills. This candidate must have 5-10 years of people management experience, including experience in managing a team of managers. S/he will have the ability to build strong and open working relationships characterized by mutual respect and an ability to build valuable business relationships outside the organization. The individual will be skilled at communicating ideas to others and inviting and considering input from others. S/he will be accessible and approachable, respecting intellectual integrity and valuing individuality. This individual will be skilled in hiring, motivating and developing talent.
? Education. An advanced degree in the business, engineering or science with an MBA from a well-regarded institution would be ideal.
- Location: Santa Clara, CA |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Application Engineer - GCMS |
| Qualifications:
- BS in Chemistry or Biology or Biochemistry or equivalent
- 5+ years hands-on experience in the field of Mass Spectrometry
- Experience with a broad range of GCMS instrumentation, ion trap and QQQ is a plus.
- Industry experience specifically providing pre/post technical support for a sales organization or providing
technical seminars to an audience is a plus.
- Excellent verbal, written and presentation communications skills
- Strong project management experience skills
- Available for flexible work schedule and business up to 75% business travel.
This position is located in the Santa Clara, CA office. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| GC/MS Applications Chemist |
| The successful candidate for this job will have:
-Advanced degree in Analytical, Physical, or Organic chemistry; or equivalent (demonstrated by 5 years working experience in analytical chemistry and confirmation of technical GC/MS knowledge).
-Demonstrated expertise in operating gas chromatographs and mass spectrometers (single and triple quadrupole, ion trap, time-of-flight)
-Ability to travel world-wide; more than 20% travel required, approximately 10% will be international. |
| Agilent Technologies, Inc. US |
San Diego |
CA |
9/4/2010
|
| Manufacturing Tech |
| Qualifications (Includes education, certifications, experience, etc.):
· Must have 5 years electrical and electronic maintenance experience.
· Must demonstrate skills/experience in electrical wiring and troubleshooting.
· Must have Knowledge and experience with digital and conventional controls systems, including Allen Bradley PLC and Wonderware control system.
· Must have the ability to read and interpret drawings and schematics.
· The ability to interact/coordinate with service contractors, engineering professionals, and vendors is preferred.
· Valid California Drivers License
· Good computer skills, including knowledge of Word, Excel and e-mail programs.
Physical Demands:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this Job, the employee is regularly required to stand; walk; use hands to finger, handle, or feel and reach with hands and arms. The employee is occasionally required to sit and talk or hear. Employees must be able to lift up to 50lbs and be able to safely manipulate heavier objects using material handling equipment, such as pallet jacks, dollies and forklifts. Specific vision abilities required by this job include close vision, color vision, peripheral vision, depth perception and ability to adjust focus. Personal protective equipment used may include: safety goggles/glasses, lab coat, earplugs, hairnet, if welding, welding jacket and mask, dust mask and respirator.
Work Environment:
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is regularly exposed to moving mechanical parts. The location of the task may require the employee to use various size ladders and be exposed to different heights. The noise level in the work environment is usually moderate. Depending on the complexity of the problem, associate will work in an environment with exposure to grease, dirt, oil and some chemicals.
GEOGRAPHIC LOCATION: LAKE FOREST, CA
NO RELOCATION OR SPONSORSHIP FOR THIS ROLE |
| Agilent Technologies, Inc. US |
Newport |
DE |
9/4/2010
|
| Manufacturing Operations Coordinator |
| Musts:
- Demonstrated ability to work in a team environment.
- Demonstrated strong communication and organizational skills.
- Demonstrated ability to read and understand written procedures and instructions.
- Demonstrated ability to perform basic math (add, subtract, multiply, divide, ratios, weights & measures).
- Demonstrated ability to make timely decisions.
- Experience with troubleshooting and applying corrective actions.
- Demonstrated ability to maintain accurate records.
- Experience working with computers: keyboarding, Windows environment.
- Demonstrated ability to manipulate small parts, manual dexterity.
- Required to bend, stoop, and reach.
- Required to remain standing for extended periods of time.
- No known allergies to chemicals used in the work area.
- May be required to lift materials per entity specified and approved limits.
- May be required to participate in medical/screening or monitoring programs.
Desired:
- Basic PC skills: spreadsheets, word processing, databases.
- Previous manufacturing experience in an ISO certified environment. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Surveillance Application Engineer |
| Bachelors or Master Degree or University Degree or equivalent plus a minimum of 3 years relevant experience, with typically 5 to 8 years practical experience. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Global Marketing Programs Manager (MPM), Services & Support |
| Requires:
- BS/MS degree in chemistry or life sciences or a related science
- 5+ yrs marketing / development experience
- Track record of success with product launches and product introductions
- Ability to solve a broad range of problems of varying scope and complexity
- Solid project management skills
- Successfully lead projects requiring coordination with other functions, customers, third parties.
- Demonstrated ability to work with global cross-functional teams
- Excellent communications skills
- Available for up to 25% travel |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Market Segment Director Academic Research (Integrated Biology) |
| ? BS or equivalent in Biology or equivalent
? MBA preferred
? 15 years' practical life science market experience, of which 10+ years' experience in either marketing or customer facing roles.
? Expertise in managing teams is required.
? Proven experience in line-management in a sales & marketing environment
? Strong leadership & coaching skills
? Excellent inter-personal and communication skills
? Writing & Presentation skills
Geo Location: California, preferably Santa Clara with an option of San Diego |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Reliability Engineer |
| You will need to have a university degree level or equivalent (complemented by a post-graduate degree and/or certification/license). You'll also bring at least 8 years' relevant experience. An accomplished leader and influencer, Agilent is where your expertise and solutions oriented approach will take you even further.
Required Qualifications:
1. BS in Engineering / Science or equivalent with a minimum of 8 years of relevant functional experience in Reliability and Quality.
2. Post Graduate and / or certification may be required.
3. Demonstrated strong communication skills particularly around the ability to translate reliability terms and concepts such as MTBF, AFR, and ALT into objectives that engineering teams can relate to and understand.
4. Demonstrated skill in teamwork within an organization and across sites as a proactive partner.
5. Demonstrated ability to provide leadership through credibility with R&D teams based on knowledge of reliability planning, relevant testing and customer advocacy.
6. Demonstrated results orientation/accountability. Ability to remain objective given conflicting or missing information and ability to identify what should be done to fill the Gap.
7. Demonstrated skill in planning and organization particularly as it applies to judgment of priorities while managing multiple projects and tasks.
This position is located in Santa Clara, CA |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| R&D engineer |
| Qualifications:
- Bachelor/Master/PhD Degree in Electrical/Electronic/Computer Engineering with >5 years related working experience
- Experience with Xilinx ISE, ModelSim, Synplify
- Experience with VHDL or Verilog
- Experience using equipment like oscilloscopes and logic analyzers for problem resolution and design verification
You will be measured on:
Technical capability and competence and ability to grow and remain technically current
Creativity in designing applicable solutions
Ability to work with a team to deliver results as committed |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| R&D Hardware Engineer |
| Qualifications:
- Bachelor/Master/PhD Degree in Electrical/Electronic/Computer Engineering with >3 years related working experience
- Knowledgeable in PCIe/modular busses, high-speed digital and memory systems, power integrity, thermal management
- Strong knowledge of digital design with emphasis on ASICs or Xilinx FPGAs
Desired:
- Nano technology/surface science or instrumentation measurement science/domain knowledge
- Strong knowledge of digital and analog hardware, FPGA or digital ASIC development principles, Verilog or VHDL, synthesis, and simulation tools.
- Knowledge of Xilinx ISE, Plan Ahead
- Knowledge of distributed clocking schemes
You will be measured on:
Technical capability and competence and ability to grow and remain technically current
Creativity in designing applicable solutions
Ability to work with a team to deliver results as committed |
| Agilent Technologies, Inc. US |
Loveland |
CA |
9/4/2010
|
| eBusiness Architect |
| ?Bachelors or Masters Degree in Computer Science, Information Systems, or other related area of study
?3+ Years experience working with Microsoft SharePoint technologies in a complex, customer facing, content management environment.
?Understanding of the technical and business challenges involved in architecting and governing a partner facing extranet environment
?Deep hands-on experience with SharePoint 2007 out-of-box capabilities especially related to content publishing.
?Demonstrated understating of the tradeoffs between out-of-box and development-based solutions.
?3+ Years experience working with Microsoft Commerce Server technologies
?Extensive experience working with business users to gather requirements and analyze these requirements to deliver to IT resources for development.
?Strong understanding of web technologies and the benefits and tradeoffs of using them including html, css, javascript, web standards, DOM, Ajax and Flash.
?Able to maintain a high level of productivity, manage multiple competing priorities, and work effectively under the pressure of time constraints in a fast-paced, complex, collaborative and team oriented environment.
?Ability to understand business objectives and present the risks and benefits for various solutions based on their ability to meet the objective, impact on resources, required budget, and ability to meet the customer's needs.
?Solid oral and written communication skills, with the demonstrated ability to communicate complex technical topics to management and non-technical audiences.
?Understanding of Project Management principles and familiarity with project implementation in a Web environment.
?Ability and desire to work within a cross-functional team environment engaging with people from multiple business units, vendors, countries and cultures.
?Passion to stay current on the latest web technologies and web design trends.
?Proficient with Microsoft applications (Word, Excel, PowerPoint). |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| N.Cal-Nevada Sales Representative |
| Successful candidate will have the following attributes:
· College Degree, preferably in technical field.
· Proven 5 years of successful sales to vacuum related industry/accounts.
· Proven results in setting priorities, multitasking, & proactive time management.
· Ability to clearly communicate with customers and factories, using computer, written and verbal communication skills. Experience in communicating and coordinating with international locations. |
| Agilent Technologies, Inc. US |
Pittsford |
DE |
9/4/2010
|
| Pre/Post Sales Applications Scientist-Life Sciences Research |
| Requires
- BS/MS degree in Biochemistry or Molecular Biology or equivalent, PhD preferred
- 3+years laboratory experience in the field of Biology and practical experience in DNA microarrays, Next-Gen sequencing and associated reagents/software
-Strong technical knowledge of the Next-Gen sequencing market (competitive technologies, target enrichment, data interpretation, etc).
- Industrial experience specifically providing pre/post technical support for a sales organization or providing technical seminars to an audience is a plus.
- Excellent communication skills
- Requires flexibility in working hours and available for up to 50% business travel.
Geographic Location: North Eastern US |
| Agilent Technologies, Inc. US |
Loveland |
CO |
9/4/2010
|
| LSCA eBiz Project Manager |
| Internal Qualifications
?PMP certified
?Expert level experience with Microsoft Project
?Bachelors or Masters Degree in Business MIS or related field plus
?5+ year?s global project management experience.
?Proven experience in managing strategic vendor relationships focusing on the performance and accountability of outsourced support and development models.
?Solid understanding of project management methodology including ability to identify and resolve issues, manages risk, develop detailed project plans and perform resource allocations. Six Sigma experience preferred.
?Ability to travel up to 25% of the time, including international travel to India.
?Excellent interpersonal, communications, collaboration, and facilitation skills and the ability to influence globally across functional and organizational boundaries overcoming language and cultural difference. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Commodity and Supplier Relationship Manager |
| Degree in Supply Chain Management, Engineering or Business Administration (bachelor/master)
· Work related experience of min. 3 years
· Knowledge of sourcing strategies and sourcing processes in the assigned Commodity.
· Knowledge of SAP and Microsoft applications
· Self-starter and team player
· Experience in project and process management.
· Highly organized and dependable to meet/exceed required objectives, yet flexible in an ever changing environment with conflicting priorities
· Ability to operate and communicate at all levels within the organization.
· Proven global team player, capable of providing mentorship for transactional buyers and who can easily interact with internal partners.
· Strong interpersonal skills
Would be an asset/added advantage:
HP, Agilent or Varian experience
Geo Location: Temporarily in Walnut Creek, CA to be permanently located in Santa Clara, CA |
| Agilent Technologies, Inc. US |
Albuquerque |
NM |
9/4/2010
|
| Field Service Engineer- Albuquerque |
| Requires BS or MS Degree or equivalent and 2 or more years relevant experience with the use, repair, routine preventative maintenance, qualification and verification of Agilent LSCA products including GC Mass Spectrometers, Gas Chromatographs, Liquid Chromatographs,GC Headspace, and Chemstation Data Systems.
Must have GC and GCMS experience.
Desired LC and ICPMS experience
Geographic Location: Albuquerque, New Mexico |
| Agilent Technologies, Inc. US |
Wilmington |
DE |
9/4/2010
|
| Product Specialist - Columns and Supplies - Mid Atlantic |
| - BS Degree in Science (Chemistry/Biology) or equivalent
- 4+ years progressive experience in chromatography applications and/or sales along with a demonstrated track record of results preferred.
- Proven ability to understand customer needs and identify solutions to non-standard tasks/queries; actively creates business opportunities.
- Ability to solve a broad range of problems of varying scope and complexity.
- Excellent communication and teamwork skills is a must.
Geo Location: Mid Atlantic Area |
| Agilent Technologies, Inc. US |
Indianapolis |
IN |
9/4/2010
|
| Product Specialist - Columns and Supplies - Midwest |
| - BS Degree in Science (Chemistry/Biology) or equivalent
- 8+ years progressive experience in chromatography applications and/or sales along with a demonstrated track record of results preferred.
- Proven ability to understand customer needs and identify solutions to non-standard tasks/queries; actively creates business opportunities.
- Ability to solve a broad range of problems of varying scope and complexity.
- Excellent communication and teamwork skills is a must.
Geo Location: Midwest Area |
| Agilent Technologies, Inc. US |
Wilmington |
DE |
9/4/2010
|
| Support Agreement Sales Specialist |
| To join our dynamic and high-achieving team, you need:
? BA/BS/MS degree in Science or Business-related field; or equivalent
? Experience in customer facing or sales role (entry 0-4 years experience, career 3 - 8 years)
? Competitive selling experience preferred
? Ability to work in a fast paced, dynamic team environment.
? Excellent verbal and written communication skills a must.
? Strong desire to interact directly with customers (via phone, email)
? Must have proficient computer skills; experience in use of database S/W applications such as Siebel, and Microsoft Office etc.
? Available for 10% travel. |
| Agilent Technologies, Inc. US |
Anaheim |
CA |
9/4/2010
|
| Manufacturing Planning Associate |
| *A Bachelors Degree plus 2 years of relevant work experience from an accredited University OR equivalent experience.
*Working Knowledge of SAP is a must
*Knowledge of Medical Device or Diagnostics a plus
*Experience working in an FDA approved facility
You'll enjoy all the support and encouragement you need to grow your skills and knowledge base. If you can bring some experience, great. If not, your positive, proactive attitude and willingness to work as part of a go-getting team are what will set you apart.
GEOGRAPHIC LOCATION: Lake Forest, CA
No sponsorship or relocation provided for this role. |
| Agilent Technologies, Inc. US |
Anaheim |
CA |
9/4/2010
|
| Planning Specialist - Expert |
| *A Bachelors Degree plus 8 years of relevant work experience from an accredited University OR equivalent experience.
*Working Knowledge of SAP is a must
*Knowledge of Medical Device or Diagnostics a plus
*Experience working in an FDA approved facility
You'll enjoy all the support and encouragement you need to grow your skills and knowledge base. Your positive, proactive attitude and willingness to work as part of a go-getting team are what will set you apart.
GEOGRAPHIC LOCATION: Lake Forest, CA
No sponsorship or relocation provided for this role. |
| Agilent Technologies, Inc. US |
Newport |
DE |
9/4/2010
|
| Chemical Process Operator |
| - Technical Associate degree or equivalent experience
- 3 to 5 years of laboratory or industrial chemical experience
- Demonstrated ability to work in a team environment
- Demonstrated strong written and oral communication and organization skills
- Experience setting up process or laboratory equipment
- Demonstrated ability to read and understand written procedures and instructions
- Demonstrated ability to maintain accurate and detailed records
- Demonstrated ability to perform basic math (add, subtract, multiply, divide, ratios, weights and measures)
- Demonstrated ability to work safely with potentially hazardous materials
- Demonstrated ability to efficiently perform job responsibilities with little daily supervision & to make timely decisions
- Demonstrated ability to adjust rapidly and effectively to change and to remain open to new ideas
- Demonstrated ability to troubleshoot issues and apply corrective actions
- Required to bend, stoop, reach, and to remain standing for extended periods of time
- Required to lift up to 50 lbs
- No known allergies to chemicals used in the work area
- May be required to participate in medical screening or monitoring programs |
| Agilent Technologies, Inc. US |
Anaheim |
CA |
9/4/2010
|
| Procurement Supervisor |
| *A Bachelors Degree plus 6 years of relevant work experience from an accredited University OR equivalent experience.
*2-5 years working knowledge of SAP is a must
*Knowledge of Medical Device or Diagnostics a plus
*Experience working in an FDA approved facility
You'll enjoy all the support and encouragement you need to grow your skills and knowledge base. If you can bring some experience, great. Your positive, proactive attitude and willingness to work as part of a go-getting team are what will set you apart.
GEOGRAPHIC LOCATION: Lake Forest, CA
No sponsorship or relocation provided for this role. |
| Agilent Technologies, Inc. US |
La Jolla |
CA |
9/4/2010
|
| Wireless Systems Application Engineer |
| Qualifications:
? BSEE or Masters degree in Engineering
? 5+ years hands-on experience with RF instrumentation including Spectrum Analyzers, Signal Sources, Power Meters
? 5+ years experience with Agilent Signal Studio, Agilent Vector Signal Analyzer, Matlab, or equivalent competitor design tools
? 3+ years hands-on R&D/development experience in Layer 1 (PHY) Wireless technologies such as GSM, GPRS, EGPRS, WCDMA (UMTS), HSPA, CDMA2000, 1xEVDO
? 3+ years hands-on experience with Cellular OBT?s such as Agilent 8960, R&S CMU200, Anritsu MT8820
Additional Skills:
? Familiarity with 3GPP, 3GPP2 (e.g. TS51.010, 34.121) test specifications
? Computer/IT admin skills; general system administration, setup, networking, and configuration mgt skills
? Software expertise; VB6, .NET, C#, Labview, scripting
? RF simulators; ADS, SystemVue
? Good customer communication skills; ability to lead customer facing technical discussions
? Office Tools; MS Word, Powerpoint, Excel, Visio, etc
? Excellent problem solving, diagnostic skills
? Strong trouble-shooting skills
? Strong team player |
| Agilent Technologies, Inc. US |
Anaheim |
CA |
9/4/2010
|
| Service Tech Specialist |
| This position requires higher education (Bachelors or Associates degree) or specialized training/certification.
? Requires a minimum of 7 years directly related experience, with typically 9 to 15 years experience
? Expert skills in the calibration and repair of all types of Agilent and Multivendor Test Equipment
? Experience using automated calibration software platforms (STE, PC Based, METCAL, TME etc) is required.
? Requires excellent communication and organizational skills. |
| Agilent Technologies, Inc. US |
Bethlehem |
PA |
9/4/2010
|
| Service Tech Specialist |
| This position requires higher education (Bachelors or Associates degree) or specialized training/certification.
? Requires a minimum of 7 years directly related experience, with typically 9 to 15 years experience
? Expert skills in the calibration and repair of all types of Agilent and Multivendor Test Equipment
? Experience using automated calibration software platforms (STE, PC Based, METCAL, TME etc) is required.
? Requires excellent communication and organizational skills. |
| Agilent Technologies, Inc. US |
Newport |
DE |
9/4/2010
|
| Operations Support Technician-2nd shift |
| Musts
- Minimum 3 years of manufacturing experience (typically 4-7 years), including hands-on knowledge of liquid chromatography systems.
- Demonstrated ability to work both independently and cooperatively in a team environment.
- Demonstrated strong communication and organizational skills.
- Demonstrated problem solving skills, including trouble-shooting to determine root cause and applying appropriate corrective actions.
- Demonstrated ability to effectively juggle multiple priorities.
- Demonstrated ability to make timely decisions.
- Demonstrated computer experience with ability to use basic Windows applications including spreadsheets, word processing, and databases.
- Required to bend, stoop, reach, and manipulate small parts.
- Required to remain standing for extended periods of time.
- No known allergies to chemicals used in the work area.
- May be required to lift materials per entity specified and approved limits.
- May be required to participate in medical screening or monitoring programs.
Desired
- Minimum 3 years of experience (typically 4-7 years) in loading, testing, and trouble-shooting liquid chromatography columns.
- Associates Degree in a technical area. |
| Agilent Technologies, Inc. US |
Newport |
DE |
9/4/2010
|
| Material Coordinator-2nd shift |
| May require some higher education or specialized training/certification.
Requires a minimum of 3 years directly related experience, with typically 4 to 6 years' experience.
Musts:
- Demonstrated ability to work in a team environment.
- Demonstrated strong communication and organizational skills.
- Demonstrated ability to read and understand written procedures and instructions.
- Demonstrated ability to perform basic math (add, subtract, multiply, divide, ratios, weights & measures).
- Demonstrated ability to make timely decisions.
- Demonstrated ability to maintain accurate records.
- Experience working with computers: keyboarding, Windows environment, spreadsheets, word processing, databases.
- Demonstrated ability to manipulate small parts, manual dexterity.
- Required to bend, stoop, and reach.
- Required to remain standing for extended periods of time.
- No known allergies to chemicals used in the work area.
- Required to lift materials per entity specified and approved limits.
- May be required to participate in medical/screening or monitoring programs.
Desired:
- Previous experience using SAP in a material coordination capacity.
- Previous manufacturing experience in an ISO certified environment |
| Agilent Technologies, Inc. US |
Wilmington |
DE |
9/4/2010
|
| Online Sales Specialist - Intern |
| Completion of sophomore/junior/senior year towards a BA/BS in Chemistry, Biochemistry, or related science degree
Would also consider Business, Marketing or similar discipline
Proficiency in the use of Microsoft Office - Excel, Word, Outlook
Strong interest in interacting directly with customers (via phone, email)
Excellent verbal, written and phone communications skills
Must be a team player with ability to work in a fast paced, dynamic team environment |
| Agilent Technologies, Inc. US |
Wilmington |
DE |
9/4/2010
|
| Online Sales Specialist - Intern |
| Completion of sophomore/junior/senior year towards a BA/BS in Chemistry, Biochemistry, or related science degree
Would also consider Business, Marketing or similar discipline
Proficiency in the use of Microsoft Office - Excel, Word, Outlook
Strong interest in interacting directly with customers (via phone, email)
Excellent verbal, written and phone communications skills
Must be a team player with ability to work in a fast paced, dynamic team environment |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Senior Product Manager / Life Sciences Marketing |
| ? 5+ years of product marketing/management experience; services marketing experience a plus
? Familiarity with Life Sciences industry and analytical instrumentation
? Track record of successful business results
? Bachelors degree in chemistry, biology or related scientific field or equivalent; MBA a plus
? Experience in leading cross-functional and international project teams
? Excellent verbal and communication skills
? Ability to travel, including international, approximately 35% of the time
? Physical work location at a major Agilent site (Santa Clara, CA or Wilmington, DE or Englewood, CO) strongly preferred |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Senior Product Manager |
| ? Minimum bachelors degree in chemistry, biology or related scientific field or equivalent; MBA a plus
? Minimum 4 years of product marketing experience; strong preference for Services Marketing experience
? Minimum of 3 years experience in marketing, selling, commercializing, managing, supporting analytical lab instrumentation or analytical lab experience, preferably in the Life Sciences industry
? Track record of business results
? Strong evidence of customer orientation
? Demonstrated ability to influence all levels of an organization, across regional/cultural boundaries and across multiple disciplines
? Excellent verbal & written communication skills.
? Ability to travel, including international
(10-30%)
Location: In Santa Clara, CA, Wilmington, DE, Englewood, CO |
| Agilent Technologies, Inc. US |
Folsom |
CA |
9/4/2010
|
| Marketing Program Manager- Spectroscopy |
| - BS/MS Degree required, science related degree desired
- MBA, or equivalent experience highly desired
- Strong domain knowledge of Spectroscopy markets and products.
- 5+ years direct field experience in a customer facing role in a closely related field with a proven track record of success in resource and relationship management skills.
- Must have previous success in direct solution selling.
- Strong business and marketing acumen
- Demonstrated successes in developing and executing business and marketing plans.
- Sales channels knowledge.
- Excellent interpersonal, leadership and team-effectiveness skills with virtual/cross functional teams.
- Ability to demonstrate sound decision making and achievement/results oriented focus skills.
- Outstanding communication and presentation skills.
Geo Location: Little Falls, DE or Santa Clara, CA preferred |
| Agilent Technologies, Inc. US |
Folsom |
CA |
9/4/2010
|
| Marketing Program Manager - Columns and Supplies |
| - BS/MS Degree required, science related degree desired
- MBA, or equivalent experience highly desired
- Strong domain knowledge of CAG and LSG markets and products.
- 5+ years direct field experience in a customer facing role in a closely related field with a proven track record of success in resource and relationship management skills.
- Must have previous success in direct solution selling.
- Strong business and marketing acumen
- Demonstrated successes in developing and executing business and marketing plans.
- Sales channels knowledge.
- Excellent interpersonal, leadership and team-effectiveness skills with virtual/cross functional teams.
- Ability to demonstrate sound decision making and achievement/results oriented focus skills.
- Outstanding communication and presentation skills.
Geo Location: Little Falls, DE or Folsom, CA strongly preferred. |
| Agilent Technologies, Inc. US |
Tigard |
OR |
9/4/2010
|
| Account Manager |
| Bachelors or Master Degree in engineering (Electrical Engineering is a plus) and a minimum of 5+ years as a strategic Account Manager
Experience selling digital & wireless test products
Strong knowledge and Experience dealing with customers in the computer, wireless, and data networking industries
The candidate must live in close proximity to Portland, Oregon |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
9/4/2010
|
| R&D Mechanical Engineer |
| - Bachelors Degree or Masters Degree in ME
- Industry experience as a Mechanical Design Engineer in R&D
- Strong written and verbal communication skills.
- Excellent teamwork skills.
- Self-starter. Willing and able to quickly learn new technologies |
| Agilent Technologies, Inc. US |
Wilmington |
DE |
9/4/2010
|
| GC/MS Manufacturing Engineering Intern - Mechanical Engineering |
| Qualifications
? Bachelors Degree in Mechanical Engineering at an accredited 4 year University.
? Excellent teamwork skills
? Excellent written and oral communication skills
? Thrive in a hands-on working environment
? High initiative
? Knowledge and interest in statistics
? Interest in Chemistry
? Good Computer skills including programming |
| Agilent Technologies, Inc. US |
Andover |
MA |
9/4/2010
|
| AgilentCARE Representative- Technical/Commercial |
| QUALIFICATIONS REQUIREMENTS
· AS Degree in Business or a related discipline and a minimum of 3 years of progressively responsible experience in a customer service, Sales/Marketing role.
· Demonstrated working knowledge of ERP database applications for Sales and Marketing administration. Experience using SAP is highly desirable.
· Knowledge with automated quoting systems is desired.
· Exceptional customer relationship management skills.
· Ability to work independently, multi-task, manage competing priorities and thrive in a fast-paced environment.
§ Proficiency with various software applications including Microsoft Power Point, Word, and Excel.
§ Strong commitment to customer satisfaction, a positive attitude and the desire and ability to work effectively in a team environment.
· Effective, professional verbal and written communications skills, including the ability to foster camaraderie and cooperation with internal and external colleagues and customers.
TRAVEL:
Domestic:
International:
SUCCESS FACTORS
§ Ability to effectively multitask in a fast paced environment where changing business needs dictate a continuous change in priority.
§ Become conversant in all products, understand where to get necessary information and use appropriate automated systems.
§ Exhibit enthusiasm, high energy and a tremendous work ethic.
§ Passion for creating an exceptional customer experience.
§ Can function independently and participate successfully in a team environment.
§ Maintain constructive relationships with internal teams. Maintain diplomacy in general communications and problem solving situations.
§ Appropriately refers to correct resources for problem solving.
PHYSICAL REQUIREMENTS
WORK ENVIRONMENT
Office environment
GEOGRAPHIC LOCATION: Lexington, MA |
| Agilent Technologies, Inc. US |
Andover |
MA |
9/4/2010
|
| AgilentCARE Representative- Commercial Specialist |
| QUALIFICATIONS REQUIREMENTS
§ AS Degree in a related field or other technical training is required
§ Minimum 3 years previous expereince in a technical call distribution center.
§ Excellent oral and written communication skills including pleasant, profesional telephone etiquette and the ability to converse fluently in Engish.
§ Proficiency with various software applications including Microsoft Power Point, Word, and Excel.
§ Prior experience with ERP database applications, SAP experience highly desired.
§ Strong commitment to customer satisfaction, a positive attitude and the desire and ability to work effectively in a team environment.
§ Highly orgnized and detail oriended
§ Basic Computer skills
TRAVEL:
Domestic:
International:
SUCCESS FACTORS
§ Ability to effectively multitask in a fast paced environment where changing business needs dictate a continuous change in priorities.
§ Can function independently and participate successfully in a team environment. Maintains constructive relationships with internal teams.
§ Appropriately refers to correct resources for problem solving.
§ Maintains diplomacy in general communications and problem solving situations. Displays a positive, cooperative and amiable demeanor
§ Commits to communicated deliverables
PHYSICAL REQUIREMENTS
Ability to utilize a Personal Computer and Telephone
WORK ENVIRONMENT
Office Environment
GEOGRAPHIC LOCATION: Lexington, MA |
| Agilent Technologies, Inc. US |
Cedar Creek |
TX |
9/4/2010
|
| Manufacturing Scientist |
| This position requires a BS/BA degree in biological science or related field and two (2) to four (4) years of previous experience in chemistry, molecular biology, and/or biochemistry or a Masters in biological science or related field and one (1) to two (2) years of previous experience in chemistry, molecular biology, and/or biochemistry. Must have hands on working knowledge of standard laboratory techniques of molecular biology (PCR, QPCR, cloning, enzymatic assays, and array technology). Strong oral and written communication, organization, team building and computer skills essential to the role.
Geo Location: Cedar Creek, TX |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Mechanical Engineer, New Product Introduction |
| Qualified applicants will possess:
? Bachelors or Masters Degree in Mechanical Engineering.
? Demonstrated knowledge of mechanical design concepts
? Experience in both 2D and 3D design
? Knowledge of GD&T and common machining techniques
? Experience in a production environment supporting hardware assembly processes
? Strong written and verbal communication skills
? Strong teamwork skills, including working in remote teams
? Experience in bringing new products to market
? Experience with HP/Agilent Product development lifecycle
? DFX Experience
Geo Location: Santa Clara, CA |
| Agilent Technologies, Inc. US |
Cedar Creek |
TX |
9/4/2010
|
| Manufacturing Scientist |
| This position requires a BS/BA degree in biological science or related field and zero (0) to two (2) years of previous experience in chemistry, molecular biology, and/or biochemistry. Hands on working knowledge of standard laboratory techniques of molecular biology (PCR, QPCR, cloning, enzymatic assays, and array technology) is a plus. Strong oral and written communication, organization, team building and computer skills essential to the role. |
| Agilent Technologies, Inc. US |
Wilmington |
DE |
9/4/2010
|
| Director of Marketing |
| Qualifications: Bachelor Degree in Sciences, Business degree or equivalent experience additionally preferred.
5+ years of product or strategic marketing experience required.
5+ years of management experience required. Proven track record of change management, teambuilding and leadership skills.
Proven track record of leading the integration and prioritization of resources across highly complex functions. |
| Agilent Technologies, Inc. US |
Wilmington |
DE |
9/4/2010
|
| Customer Account Specialist |
| Qualifications:
? BA/BS in Chemistry, Biochemistry, or related science degree
? Strong interest in interacting directly with customers (via phone, email)
? Ability to travel to domestically and internationally 3-4 times per year. |
| Agilent Technologies, Inc. US |
Wilmington |
DE |
9/4/2010
|
| Implementation Specialist |
| Qualifications:
? BA/BS in Business, Chemistry, Biochemistry, or related science degree
? Strong interest in interacting directly with customers (via phone, email)
? Ability to travel to internationally 1-2 times per year.
Geo Location: Wilmington, DE |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Mixed-Signal/RF IC Designer |
| Education:
Ph.D. in Electrical Engineering or closely related field with thesis work on mixed-signal IC design preferred. Candidates should have designed, have had fabricated and characterized a mixed-signal or RF integrated circuit as a central portion of their relevant thesis work.
M.S. in Electrical Engineering with experience in or substantial coursework related to mixed-signal IC design required. Candidates not possessing a Ph.D. degree must have completed the design, have had fabricated and characterized a mixed-signal or RF integrated circuit of complexity and performance commensurate with that of a Ph.D. thesis. In addition, two years relevant full-time employment experience or full-time graduate study is required post M.S. degree.
Qualifications:
Must have experience in the design of high-speed analog, mixed-signal or RF integrated circuits.
Substantial involvement in the design of transistor level circuits for inclusion on an IC, physical design of ICs, and the test and characterization of an IC.
Strong understanding of transistor physics and EM theory and their impact on circuits. Experience in 2-D and 3-D electromagnetic simulation of on-chip structures and derivation of a model for use in circuit simulators is highly desired.
Ability to synthesize multiple solutions to a given problem and the ability to critically analyze the strengths and weaknesses of each.
Experience with modern EDA tools used in IC design including simulation, schematic capture, physical layout and verification.
Familiarity with programming and scripting languages to enable automation in the design, simulation and testing of ICs.
Demonstrated ability to work well in a team environment is a must. Ability to document and present results.
Preferred Qualifications:
Experience with the use of both sub-micron CMOS and modern SiGe bipolar devices (fT > 150 GHz) in analog, mixed-signal, or RF integrated circuit design.
Experience with PLLs, clock-data recovery circuits, and data converters.
Experience with custom high-speed digital data paths.
Experience with a synthesized digital design flow, from a high-level HDL to transistor level artwork.
Experience with mixed-mode simulation of analog and digital blocks -- mixed-signal or behavioral modeling of analog circuits.
Experience with device modeling, thermal design, IC package design. |
| Agilent Technologies, Inc. US |
Cary |
NC |
9/4/2010
|
| Production Manufacturing Supervisor |
| ? Will have a bachelor?s degree in a technical or operational field.
? Will have a minimum of five years of experience as supervisor preferably in high precision technology product manufacturing.
? Extensive knowledge of lean manufacturing process activities and quality management system requirements.
? Proficiency with SAP or other ERP systems and Microsoft Office Applications.
? Proficiency in verbal and written English. |
| Agilent Technologies, Inc. US |
Englewood |
CO |
9/4/2010
|
| Application Engineer |
| Agilent is looking for new college graduates with a minimum BSEE or BSEET degrees. We not only pride ourselves on hiring students with strong technical backgrounds, but also with excellent communication skills. The ability to communicate your thoughts, ideas, and point of view is very important in this position and to the long-term development of your career. You must demonstrate the ability to work closely in teams and understand the dynamics of a team environment. We are looking for candidates that have demonstrated leadership skills and have the ability to be dynamic and persuasive in a professional setting. |
| Agilent Technologies, Inc. US |
Dallas |
TX |
9/4/2010
|
| Academic Account Manager - Texas |
| Requires
- BS/MS in a Life Science discipline (advanced degree preferred) and
- 2+ years direct sales or lab experience with a demonstrated track record of success
- High level of expertise in Liquid Chromatography including a working knowledge of Fast LC (UHPLC)and LCMS.
- Proteomics/biochemistry product expertise within varied industries and customer types.
- Strong business development and sales/closing skills.
- Must have excellent communication (written and verbal) and teamwork skills.
- Able to interface comfortably at high levels within the customer management structure |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
9/4/2010
|
| R&D ASIC Engineer |
| Minimum Qualifications:
BS or MS in Electrical Engineering or Computer Engineering
? Exposure digital VLSI design
? Demonstrated Verilog/System-verilog design
? Knowledge of semiconductor devices and structures
? Understanding of physical implementation
? Understanding of analog design basics
? Understanding of digital ASIC design methods, tools and verification methodologies
? Understanding of physical VLSI ASIC design methods and tools
? Strong multi-tasking and teamwork skills
? Strong verbal and written communication skills
? Ability to understand systems and digital architectures
? Strong understanding of engineering mathematics |
| Agilent Technologies, Inc. US |
Santa Rosa |
CA |
9/4/2010
|
| New Product Manufacturing Engineer |
| Position requires
? BS/MS in Electrical/Electronic Engineering
? 3+ years Experience in the design or manufacturing engineering of RF and Microwave (MW) test instrumentation
? 3+ years Experience with New product Introduction (NPI) of RF and Microwave (MW) test instrumentation products
? Experience creating electrical product design or manufacturing test processes and technical documentation of these processes
? Experience with evaluation of new product designs to ensure manufacturability
? Sound knowledge of equipment calibration standards
? Experienced in setting manufacturing product specifications and statistically analyzing product performance
? Sound understanding of instrument measurement uncertainty analysis in accordance to stringent calibration lab requirements eg. ISO17025
? Programming in one or more of the following
o Unix, Linux, RMB, VB, C, C++, VEE, Labview, .NET (dotnet)
? Ability to interact effectively with people at all levels
? Strong knowledge of test instrument application & usage will be an added advantage
? Knowledge or experience in project management will be an added advantage |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Associate Engineer, R&D |
| List minimum education, training and experience needed to perform this job:
1. BSEE/BSET or 3 or more years of related experience.
2. Proficient in RF circuits a plus.
3. Knowledge of Network Analyzer, Signal Generator, Oscilloscopes, etc?
4. Experience with vacuum and cryogenic equipment a plus.
5. Proficient in Excel, MS Word and knowledge of Unix/Linux.
6. Domestic/ International travel; valid passport required. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Hardware Engineer-Cryogenics |
| List Minimum education, training and experience needed to perform this job:
1. BS Mechanical Engineering or related field
2. minimum 10 years experience with cryogenic and vacuum systems
3. fluent with CAD tools and thermal analysis programs
4. fluent with rf measurement tools including network analyzers, spectrum analyzers, noise figure, etc.
5. familiarity with NMR is a plus |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Hardware Engineer-Materials Science |
| List Minimum education, training and experience needed to perform this job:
1. BS Materials Science or related field
2. minimum 3 years experience with cryogenic systems
3. fluent with CAD tools and thermal analysis programs
4. fluent with rf measurement tools including network analyzers, spectrum analyzers, noise figure, etc.
5. familiarity with NMR is a plus |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| R&D Hardware Engineer-Modeling |
| List Minimum education, training and experience needed to perform this job:
1. MS EE or Physics
2. fluent with rf modeling programs
3. fluent with rf measurement tools including network analyzers, spectrum analyzers, noise figure, etc.
4. familiarity with NMR is a plus |
| Agilent Technologies, Inc. US |
Menlo Park |
CA |
9/4/2010
|
| Manufacturing Technician, New Product Introduction |
| Qualified applicants will possess:
? AA/AS degree in Mechanical or Electrical Engineering Technology, or an equivalent combination of education and work experience
? Strong organizational skills to efficiently manage large quantities of prototype material
? Production line experience building or repairing electro-mechanical assemblies
? Soldering and PCA repair experience
? Demonstrated computer skills in word processing, spreadsheets, and presentations
? Initiative and ability to work independently
? Flexibility to work in a wide variety of roles to support prototype development
? Strong written and verbal communication skills
? Experience working on a cross-functional team
Geo Location: Santa Clara, CA |
| Agilent Technologies, Inc. US |
Boulder |
CO |
9/4/2010
|
| API Process Development Scientist |
| Requires:
- BS/MS or PhD Chemistry, Biochemistry; or Life Science discipline or equivalent
- 3+ years hands on process development experience in pharmaceutical or biotechnology industrial
- Pharmaceutical pilot palnt experience desired
- Downstream and purification experience desirable
- Hands on experience with HPLC, GC-MS, LC-MS, MS-MS, NMR and other supporting analytical technologies for chemical synthesis
-Experience with DOE, statistical process control, Process Analytic Technology (PAT) applications and Quality by Design (QbD) initiatives desired
- A proven track record in product/process development of API's that have been successfully transferred validated and approved by the FDA or corresponding regulatory authority.
- Experience in development and successful transfer of safe, robust and scalable processes for the preparation of APIs.
- Knowledge of ICH Q7 and cGMP guidelines highly desired
- Excellent communication (oral and written), computer skills and interpersonal skills a must
- Ability to interface with global cross-functional internal and external customers and partners
- Track record of success in working with multiple projects in a fast pace environment managing to aggressive time lines and deliver projects on time
- Available for occasional business travel
Geo Location: Boulder, CO |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Product Manager - Genomics |
| Requires:
- BS in biology, biochemistry, molecular biology; related discipline or equivalent. Master or PhD preferred.
- 5+ years experience in marketing life science products.
- Demonstrated use of marketing skills and market knowledge to define and commercialize products that result in business success
- Experience in working with worldwide customers and is a strong advocate for customer focus and customer driven development
- Demonstrate ability to develop marketing plans that align with strategic objectives
- Ability to work independently to plan, prioritize workload, schedule time, assess and solve problems
- High proficiency in pricing and forecasting
- Must exhibit strategic thinking, teamwork, creativity, planning and organization, and flexibility
- Strong analytical and decision making skills
- Experience in working with global markets/customers an advantage
- Excellent written and oral communications skills and comfortable presenting to high level audiences both internally and externally
- Must have flexibility in working hours and available for 25% business travel
Geographic Location: Santa Clara, California. |
| Agilent Technologies, Inc. US |
Boulder |
CO |
9/4/2010
|
| North American Pharmaceutical API Sales |
| ? BS/MS in Chemistry or a Life Sciences discipline, or equivalent.
? 5+ years related direct sales experience selling Life Sciences products/services
? A demonstrated track record of successfully selling against a quota.
? High level of experience interacting with senior level customers from biopharma companies.
? Knowledge of drug development and CMC processes
? Working knowledge of competitive products (services, value propositions, price points).
? Demonstrated commercial selling skills. Strong business development and sales closing skills
? Effective interpersonal communication and telephone sales skills.
? Knowledge of DNA/RNA manufacturing and analysis technology highly desired
? Must be able to travel up to 50% of the time. |
| Agilent Technologies, Inc. US |
Cedar Creek |
TX |
9/4/2010
|
| Planner |
| You will need to be educated to at least university degree level and have at least 3 years' experience at a similar level. Your excellent organizational skills, vision and solutions-oriented approach are what will set your apart.
Geo location: Cedar Creek, TX |
| Agilent Technologies, Inc. US |
Menlo Park |
CA |
9/4/2010
|
| Integration Manager ? Mergers, Acquisitions, and Divestitures |
| Candidates should have worked in multiple functions and have at least 5 years? project management experience managing various projects of increasing responsibility, a Bachelors or Masters degree (MBA preferred), plus:
?Proven success at influencing and leading resources across multiple functions, workgroups, and management levels
?Established credibility with upper management
?Demonstrated excellent project management, communication, and teamwork skills
?Ability to formulate the big picture while working on project details
?A tolerance for ambiguity and flexibility to changing projects and priorities
?Must work at Santa Clara site, not remotely
?Desired: A strong finance background as well as familiarity with legal contracts. |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Future Sales Opportunities |
| Specific requirements include:
· Experience calling on health care providers in hepatitis, hepatology, gastroenterology, virology, or infectious disease
· Proven results orientation / Top ranking in your sales force
· Strong understanding of legal and regulatory environment
· Passion and dedication to providing high quality customer service
· Team Player ? ?We Wins? is one of our key values
· Desire to be part of a new and growing commercial organization ? opportunity to launch a drug!
As our sales force hiring plans develop, we will contact you if your background matches these requirements to discuss opportunities with Vertex.
Positions are available across the US in both field sales and sales management.
Thank you for your interest in Vertex Pharmaceuticals.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Medicinal Chemist/ Research Scientist I |
| This position requires a MS in Synthetic or Medicinal Chemistry and at least 3 years experience as a medicinal chemist in an industrial setting with a proven record of achievement or a PhD and a post doc in Synthetic or Medicinal Chemistry.
Excellent communication skills are required, as the successful candidate will be expected to interact with scientists in other disciplines on a daily basis. Experience with Structure based design a plus.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Senior Research Associate |
| B.S./M.S. in Biological Sciences/Chemistry or related field with minimum of 4 years of working experience. Hands-on experience with in vitro ADME studies are required as well as experience with design, execution and data interpretation of these in vitro studies. Experience with analytical techniques (HPLC and mass spectrometry) are a plus.
Must be highly motivated, organized with excellent communication skills (both oral and written), detail oriented, and a good team player
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Senior Clinical Staffing Consultant |
| ? 5+ years pharmaceutical clinical or medical recruiting experience a must, minimum of a Bachelors degree or equivalent
? Experience working in a fast-paced, highly matrix organization
? Proven track record of finding unique ways to source and attract qualified candidates
? Superior selection skills and a high level of proficiency in assessing individuals
? Proven ability cultivating successful relationships internally and externally
? Results driven, ability to demonstrate/quantify success relative to established targets and metrics
? Strong listening, facilitation and communications skills
? Strong organizational, multi-tasking and computer and web skills, along with the ability to handle sensitive and confidential situations/information
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Analytical Chemist, Scientist I |
| - A Ph.D. or Master's or Bachelor's degree in the life or physical sciences with a preference for a concentration in Chemistry, Analytical Chemistry or Pharmaceutical Chemistry
- 0 - 3 years (PhD), 3 - 5 years (MS) or 6+ years (BS) current relative industry experience working in drug substance and drug product support
- Scientist II: 3 - 5 years (PhD), 5+ years (MS) or 8+ years (BS) current relative industry experience working in drug substance and drug product support
- Broad understanding of the drug development process, including clinical design, chemical development, and formulation development, especially how those processes impact analytical method development, validation, and method transfer are essential
- High level understanding of risks in all aspects of method development, validation and transfer and the ability to use risk analysis and quality- by-design approaches to develop robust methods, design appropriate validation protocols to validate methods for their intended use, and ensure successful method transfer are essential
- Good understanding of ICH and FDA method validation guidelines are essential. The ability of identifying areas overlooked in the guidelines is preferred.
- Good understanding of GMP and hands-on GMP experience as well as how to develop methods that are GMP friendly are preferred.
- Skilled in HPLC, LC-MS, GC, GC-MS, FT-IR, UV-VIS, KF, NMR, dissolution and other instruments
- The ability to work successfully in both a team/matrix environment as well as independently
- The ability to work in a fast pace environment, manage priorities, and maintain timelines for multiple projects
- Excellent written and verbal communication skills
- Established organizational skills
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Principal Statistical Programmer |
| * B.S. in Biostatistics, Statistics, Computer Science, or a related field and a minimum of 10 years of SAS and relevant pharmaceutical industry experience
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Associate Director, Medical Affairs Program Management |
| ? Ability to lead a matrix team
? Ability to complete goals within allotted timeframes and deliver high quality results
? Ability to initiate, plan, and complete projects
? Strong initiative and ability to identify issues and create solutions
? Knowledge of Hepatitis C and/or Cystic Fibrosis therapeutic areas preferred
? Program management experience highly desired
? Ability to use Microsoft Office programs
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Senior Medical Director, CF |
| · MD, DO or international equivalent
· Minimum of 5 years pharmaceutical industry experience, including time managing clinical trials and/or clinical development program(s)
· Preferred qualifications include sub-specialty training in internal medicine, family practice, pediatrics, pulmonary medicine, allergy, and/or industry background
· Board certification/eligibility in specialty area
· Ability to work collaboratively in a challenging team matrix environment
· Ability to work independently to resolve challenges and conflicts
· Possess a comprehensive understanding of applicable US and EU regulatory requirements and of the drug development process
· Have a working knowledge of biostatistics, data management, clinical operations and clinical pharmacokinetic scientific and technical processes
· Experience in filing and defending US INDs and/or NDAs
· Excellent communication skills
· Willing to re-locate to the Cambridge area
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Medical Director |
| ? MD, DO or international equivalent
? 2+ years of basic or clinical research experience in an academic setting with publications in peer reviewed journals
? 5+ years of experience in Clinical Development in the pharmaceutical industry
? Board certification in Internal Medicine, Infectious Disease or other relevant medical specialty
? Excellent communication skills
? Ability to work collaboratively in a team-based matrix management environment with minimal supervision
? Possess a full understanding of applicable US and EU regulations and of the drug development process
? Have a working knowledge of biostatistics and pharmacokinetics
? Experience in filing and defending US IND's or similar ex-US regulatory submissions
? Preferred qualifications include sub-specialty training in internal medicine, infectious disease (HCV), family practice, pediatrics, pulmonary medicine or allergy.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Associate Director, CLinical Pharmacology |
| * PharmD or Ph.D. and 5+ years of industry experience
* NCE drug development experience with at least 5 NCEs in the past
* Possesses good knowledge of drug Development Programs and a keen awareness of development issues
* Able to integrate the activities of distinct functional groups across multiple projects
* Can recognize and carry out productive new development initiatives/directions Is a mid-level experienced mentor who effectively infuses confidence and team commitment: can make clear written and oral presentations.
* Exhibits a record of excellent operational and ethical standards, and team-improvement
* Demonstrated ability to provide career development to staff
* Able to recognize and resolve important organizational problems and/or infusing innovation Has leadership abilities, can initiate and carry out tasks with little direct supervision
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Analytical Chemist/ Sr. Scientific Associate |
| - A Bachelor's degree in the life sciences or physical sciences with a preference for a concentration in Chemistry, Analytical Chemistry or Pharmaceutical Chemistry with 3-5 years related experience.
- Working understanding of DISSOLUTION, HPLC, LC-MS, GC, GC-MS, FT-IR, UV-VIS, KF, and other instruments used in the analysis of pharmaceutical products
- An interest in and passion for establishing a career in analytical development and the biopharmaceutical industries
- The ability to work successfully in both a team environment as well as independently
- Excellent written and verbal communication skills
- Established organizational skills
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Associate Medical Director |
| * MD, DO or equivalent ex-US medical degree (Non-MD candidates with doctoral degrees will be considered if they have an appropriate background in a clinical field)
* 1-2 years of basic or clinical research experience in an academic or industrial setting with experience in publications
* Clinical drug development experience and excellent communication skills
* Ability to work collaboratively in a team-based matrix environment and to function autonomously as appropriate
* Possess a full understanding of applicable US and EU drug development regulations and GCP regulations
* Have a working knowledge of biostatistics and pharmacokinetics
* Experience in interactions with regulatory authorities
* Willing to re-locate to the Cambridge area
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Sr. Marketing Manager, HCV Marketing |
| - A Bachelor?s degree with a preference for an MBA or advanced degree
- Minimum of 5 years related experience in the pharmaceutical and/or biopharmaceutical arena, including some combination of the following: marketing, sales, or market research. Product launch and/or specialty pharmaceutical experience (especially in HCV/hepatitis) is greatly preferred.
- A strong understanding of the legal and regulatory environment
- An entrepreneurial spirit and ability to develop solutions to complex problems requiring the use of innovation, ingenuity and creativity
- Results oriented and excellent analytic, strategic, business planning, communication and collaboration skills
- The ability to manage complexity and ambiguity in a highly matrixed environment
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Associate Director, HCV Marketing |
| - A Bachelor?s degree with a preference for an MBA or advanced degree
- A minimum of 10 years progressive experience within the biotech/pharmaceuticals industry, with at least 5 years of management experience. Marketing experience in HCV / Hepatitis / Category experience as well as product launch experience greatly preferred.
- A strong understanding of the legal and regulatory environment
- An entrepreneurial spirit and ability to develop solutions to complex problems requiring the use of innovation, ingenuity and creativity
- Results oriented and excellent analytic, strategic, business planning, communication and collaboration skills
- A strong track record in both sales and marketing is preferred
- The ability to manage complexity and ambiguity in a highly matrixed environment
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Director, Field Planning & Effectiveness |
| ? Experience in managing projects related to pharmaceutical/biotech sales force sizing, field force reporting, data management, and incentive compensation
? Solid project management and interpersonal/communication skills in leading and directing teams to achieve project objectives and goals within assigned timelines
? Thorough understanding of sales data tracking systems, processes, and methodologies
? Highly effective presentation skills, written and verbal communication skills
? Strong analytical skills, demonstrated by the ability to identify and understand complex issues and problems within product sales and prescriber information data sets
? Demonstrated ability to work independently and manage multiple projects that require collaboration across functional areas
? Team player able to develop rapport and credibility with field and home office personnel including management
? At least 3+ years experience managing small teams of employees ensuring their professional development
? MBA preferred with at least 6 years pharmaceutical/biotech industry experience in related area of responsibility
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Sr. Manager, Commercial Compliance |
| ? Thorough understanding of federal and state fraud and abuse laws, including the anti-kickback regulations, the Office of Inspector General reports, and the Food, Drug and Cosmetic Act and understanding of the roles and authority of government agencies and industry cooperative groups including FDA, OIG, and PhRMA
? Extensive experience in managing projects related to commercial pharmaceutical/biotech compliance
? Proven ability to negotiate and partner with others to resolve conflicts
? Ability to handle sensitive, confidential matters and exercise sound discretion and judgment
? Solid project management and interpersonal/communication skills in leading and directing teams to achieve project objectives and goals within assigned timelines
? Demonstrated ability to work independently and manage multiple projects that require collaboration across functional areas
? Team player able to develop rapport and credibility with field and home office personnel including management
? Bachelor?s degree required with at least 5 years pharmaceutical/biotech industry experience in related area of responsibility, legal/regulatory experience a plus.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Payroll Clerk |
| Education / Experience:
? Bachelors Degree in Accounting, Finance, or equivalent experience, CPP preferred.
? Minimum 3-5 years experience processing full cycle payroll and commissioned based employees, preferable through Ceridian.
? Advanced knowledge of applicable rules and regulations required for payroll administration.
? Proven experience in researching inquires and driving resolution in a timely manner.
? Exceptional communication, interpersonal and high level of organizational skills.
? Ability to manage time lines and deliverables.
? Strong customer service expertise.
? Strong technical skills with systems.
? Proficient in Microsoft Office suite of products.
? Ability to be flexible and work in dynamic, fast-paced environment managing multiple tasks.
? Ability/experience working with employees at all levels in the organization and across all functions.
? Self-starter with the ability to multi-task.
? Ability to handle confidential and sensitive information.
? Accuracy and attention to detail is a must.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Senior Compensation Specialist |
| ? Bachelors Degree in Business Administration, Accounting, Finance or related field
? Must have a minimum of 5 yrs of compensation experience; pharmaceutical industry experience preferred
? Excellent analytical skills including the ability to analyze a variety of data, determine validity, draw conclusions & make recommendations
? Advanced proficiency of Microsoft Excel
? Proficiency with Microsoft Word & Power Point
? Experience working with HRIS (Peoplesoft, Oracle, SAP, SuccessFactors) preferred
Other Skills and Abilities:
? Excellent organizational skills and attention to detail
? Excellent communication skills
? Flexible, adaptable and open to change
? Use of good judgment
? Well developed analytical and problem solving skills
? Works harmoniously and effectively with others as part of a team
? A self-starter who desires to show ownership and commitment to the job
? Exercises confidentiality and discretion
? Action oriented, with a focus on continuous improvement; also high energy with a challenging but positive style.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Sr. QA GMP Auditor/ Specialist |
| Auditing background, and ability to work/contribute in a team based environment as a lead and an participant, exceptional interpersonal skills, and adept problem solving skills are strongly desired. In addition, the candidate should have willingness to cross train in activities related to GLP and GCP is important. The candidate will also have experience in the creation of standard operating procedures (SOP's).
Three to five years of experience minimum working in a pharmaceutical Quality Assurance environment or related environment
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Director, Revenue Cycle |
| Education:
BS with a major in Accounting, CPA, MBA preferred
Experience:
Ten plus years experience in an accounting environment, preferably within a pharmaceutical company. Five plus years supervisory experience.
Preferred Skills/Qualifications:
Microsoft suite of software (Excel, Word, etc.).
Experience with Oracle Financial Software a plus
Skills/Competencies:
Excellent communication and organizational skills.
Ability to work independently with strong attention to accuracy and detail
Other Skills:
Ability to communicate effectively with higher levels of management.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Director, Internal Controls |
| * Ten or more years of business experience, including auditing, consulting and/or management experience is required.
* Experience managing Sarbanes Oxley compliance is required.
* Degree in business from accredited college or university is required. MBA preferred.
* Pharmaceutical industry experience highly preferred.
* Professional certification preferred (CPA and/or CIA).
Skill Requirements:
The new Director of Internal Controls must be an outstanding leader of uncompromising integrity along with the necessary credibility, expertise and experience required to lead the Internal Controls function within this Company to the next level.
He/She will bring a comprehensive understanding of the complexities of SOX and internal controls within a Company with complex transactions. Specifically he/she should meet the following criteria:
* Excellent interpersonal and oral and written communication skills which allow the candidate to relate well to all levels of management.
* Skill and courage to confront difficult issues with the appropriate response and communicate appropriately and in a timely manner with all stakeholders in those issues.
* Comprehensive knowledge of auditing practices, procedures and principles sufficient to interpret and analyze complex concepts.
* Understanding of financial and operational risks, control design, and technical accounting knowledge associated with generally accepted accounting principles.
* Driven to deliver quality results on time, with a high degree of integrity and in a highly ethical and professional manner
* Ability to thrive in an environment of change
* Strong technical accounting and analytical skills.
* Highly self-motivated individual who will provide leadership and guidance to staff.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Sr. Scientific Associate |
| * Bachlor's degree in Chemistry, pharmaceutical sciences, or equivalent concentration.
* 0-3 years experience in an analytical capacity;
* Have received general training/coursework on analytical instruments;
* Able to conduct dissolution analysis on solid oral dosage forms (training will be provided);
* Have an understanding of the theory of analytical development, general HPLC use and care;
* Awareness of USP dissolution methods
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. QA Specialist |
| * Bachelor's degree preferred
* 2 years of experience in Quality
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Manager, Health Value & Outcomes Research |
| Minimum Requirements:
? A bachelor?s degree in the life sciences, business administration or a related field with a preference for an advanced degree (MD, PharmD, MPH, MS, MHA or MBA). Educational focus in the areas of health economics or outcomes research would be beneficial
? 3 - 5 years of current experience with health economics and outcomes research for the biotechnology or pharmaceutical industries
? Working experience with economic modeling and payer market access tool creation
? Familiarity with payer dossiers, epidemiology, economic analyses, reimbursement and pricing environments
? A track record of success functioning in dynamic, matrix environments with the ability to multitask and adapt to rapid changes
? Exceptional written and verbal communication skills along with the ability to interact constructively across all levels of an organization and with thought leaders and other external collaborators
? The ability to effectively present technical data and complex concepts to diverse audiences
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Research Associate I |
| Experience working in a laboratory with skills in cell culture and standard molecular biology techniques (e.g., cloning and PCR) is required. Additional knowledge or experience in cell-based assays is desired. Meticulous attention to the details and regular maintenance of laboratory notebooks is required. The successful candidate must be a demonstrated team player and be able to work closely and responsively with their supervisor. Applicant must be able to follow appropriate biosafety procedures for working in an infectious disease laboratory.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Scientific Associate II |
| Minimum Education Requirements:
Bachelor?s degree in science or engineering field. Internship or undergraduate research project involving analytical laboratory work strongly preferred.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| HR Assistant |
| A Bachelor?s degree or relevant experience, 1 to 2 years of HR experience, preferably in Benefits. Flexible, adaptable and the ability to work in dynamic, fast-paced environment managing multiple tasks. Exceptional organizational and communication skills. Experience coordinating meetings including all logistics. Ability/experience working with employees at all levels in the organization. Ability to handle confidential employee information and to handle sensitive employee related issues. Lotus Notes, Word, Excel and PowerPoint skills and HRIS systems needed (Oracle HRIS experience a plus). Demonstration of Vertex?s Core Values: Fearless pursuit of excellence, innovation is our lifeblood and ?WE? wins.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Senior Business Analyst/Project Manager |
| Qualified applicants will have a Bachelor?s degree in Computer Science or Management Information Systems and a minimum 10 years experience as a Project Manager working in an Information Systems group (preferably within the Pharmaceutical of Life Sciences industry). PMP certification preferred.
Experience with Oracle E-business Suite (Oracle Project Accounting, Accounts Payables, General Ledger, Cash Management, Fixed Assets, iProcurement, Purchasing, Order Management, Accounts Receivables, Alerts, Approvals Management Engine (AME), and Application Desktop Integrator (ADI)). MicroStrategy, Kaplan, Concur, Hyperion, Cognos, Noetix, Kenexa , iManage, KBX, Ceridian and Outlooksoft is a plus.
Skills and capabilities:
* Strong project, program and portfolio management skills
* Strong leadership and team facilitation skills
* Strong business and process analysis skills
* Strong knowledge of industry solutions and best practices
* Strong communication and presentation skills
* Strong conflict management skills
* Strong negotiation and influencing skills
* Strong networking skills
* Strong time and meetings management skills
* Interpersonal, facilitative, consultative, responsive
* PC skills include: MS Project, MS Visio, MS Office
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Archive Associate |
| PREFERED EXPERIENCE AND EDUCATION:
? B.S. with relevant work experience or A.S. with an equivalent combination of education, training and industry working experience
? Attention to detail
? Knowledge of GLP/GCP
TECHNICAL AND COMMUNICATIVE SKILLS:
? Demonstrates good communication skills both oral and written
? Possesses competent computer skills
? Demonstrate excellent customer service skills.
? Be able to work well within a team environment as well as independently
? Emerging knowledge of safety requirements and regulations
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Associate Director/Director of Business Development |
| ? Medical or scientific education - a Masters degree at minimum, a PhD/MD degree is preferred.
? Relevant business experience (pharmaceutical, biotech, venture capital, investment banking, an MBA in addition will be favorably viewed).
? 3-5 years of business development experience; deal sheet demonstrating experience and past successes.
? Ability to forge relationships internally, as well as externally.
Skills / Competencies
? Able to work independently, as well as part of a team.
? Strong interpersonal skills, ability to persuade and motivate others.
? Ability to synthesize and summarize a complex set of facts and set opportunities within the broader strategic context.
? Adept at handling multiple projects and tight deadlines in a fast-paced environment.
? Strong project management, presentation and communications skills.
? Able to build and maintain contacts with potential partner companies
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Senior Formulation Development Scientist |
| - A degree in pharmaceutical sciences, chemistry, chemical engineering, materials science or related field
- PhD (or equivalent degree) and 4+ years of productive, relevant work or postdoctoral experience
- M.Sc. (or equivalent degree) and 7+ years of productive, relevant work experience.
- B.Sc. (or equivalent degree) and 10+ years of productive, relevant work experience.
- Proven ability to apply the principles of the basic sciences such as physical and organic chemistry, thermodynamics, and materials science, to formulation and process development, using a rational, scientific approach.
- Demonstrated ability to develop solutions to complex problems with creativity and innovation
- Formulation development experience on solid oral dosage forms is preferred, especially experience with small molecule NCEs and poorly soluble compounds
- Experience with a range of dosage forms, including liquids, solids and oral, iv formulations, controlled release and pediatric applications would be advantageous
- Expertise in process scale-up and optimization from laboratory scale to pilot scale and registration scale as well as familiarity with engineering scale-up principles, i.e., dimensional analysis.
- Experience applying statistical approaches in the design and analysis of experiments would be advantageous
- Experience working with and managing interactions with contract manufacturing vendors
- Inventive and innovative, self-starter who is comfortable and successful working in a multi-disciplinary team under defined timelines
- Proven teamwork, leadership and collaboration skills, with a demonstrated ability to interact and influence manage all levels of business
- Excellent verbal and written communication skills
- Demonstrated strategic planning, and organizational skills
- Supervisory experience would be a plus but not necessary
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Formulation Development Scientist II |
| A PhD or MS degree (educational concentrations in chemistry, pharmaceutics or engineering preferred)
?Pharmaceutical industry experience of 2-5 years for PhD and 5+ years for MS
?Experience working with small molecule new chemical entities (NCEs) and exposure to early phase formulation development activities
?Experience with a range of dosage forms, including liquids, solids and oral. Experience with IV formulations as well as formulation development for poorly soluble compounds would be advantageous
?Proven experience managing the scale-up and manufacturing of solid oral dosage forms
?Proven ability to apply the principles of the basic sciences, such as physical and organic chemistry, thermodynamics, and materials science, to preformulation and formulation development, using a rational, scientific approach.
?Experience applying statistical approaches in the design and analysis of experiments would be advantageous
?A history of success working in environments defined by innovation and initiative
?Ability to work effectively and comfortably in a multi-disciplinary team under defined timelines
?Excellent leadership, teamwork and organizational skills
?Solid verbal and written communication skills
?Supervisory experience would be a plus but not necessary
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Sr. Systems Analyst-BI Reporting |
| Minimum Requirements
? Enterprise BI Reporting platform (MicroStrategy, Noetix, Cognos)
? Languages: SQL, PL/SQL, Java, scripting languages
? Databases: Oracle 11g (preferred), 10g
? OS: Linux, Windows
Preferred technical skills (a plus):
? Data Warehouse design and modeling (Oracle preferred)
? Experience with all phases of software development, including requrements, design, development and testing
? Experience with Extract-Transform-Load processes and batch data movement at the enterprise level
Technical and Communication Skills:
? Ability to work interactively with users, management and support team.
? Ability to work within established coding and documentation standards
? Team contributor with good communication skills and strong analytical, problem solving skills.
Preferred Education and Experience Levels:
? B.S and 5 years relevant work experience
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Database Developer/Engineer |
| Desired Skills:
MySQL, Linux, bash,
Nice to have:
Perl, Python, ColdFusion, Java, TalenD, ETL
Experience in working in all phases of the development cycle.
Experience maintaining and developing high availability MySQL RDBMS with replication.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Research Scientist II |
| The ideal candidate for this position will be highly motivated and minimally have an MS degree with at least 10 years, or a PhD or DVM with at least 8 years of hands-on experience in using relevant general/safety pharmacology assays, such as cardiovascular telemetry or Langendorff heart perfusion.
Extensive understanding of cardiovascular pharmacology and physiology is required. Demonstrated independent thinking, trouble-shooting skills, and ability to analyze, interpret, and translate physiological function data is a must. Industry non-clinical research experience and experience with assessing drug-induced QT prolongation is preferred. Extensive knowledge of Data Sciences International/Ponemah (P3P and DataQuest), EMKA Technologies, or similar software packages is necessary. Ability to write basic programs using SAS software for data analysis and statistics is a plus.
The candidate must be able to work independently and in a matrix and function team environment. Strong written and oral communication skills are required, including excellent report writing and presentation skills. Study outsourcing and/or supervisory experiences are a plus.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Senior Director, Safety Operations |
| - M.D. or Masters /Doctorate level in life sciences or allied health fields preferred; Bachelor degree in life sciences or allied health fields required; 8+ years of direct Pharmacovigilance experience
- Solid knowledge of safety database operations and function
- Strong knowledge of Global Regulations, standards and best practices regarding safety processing and reporting, safety surveillance and pharmaceutical industry compliance activities in pre-marketing and post-marketing
-Strong operational skills as demonstrated by leading previous projects or functions and or equivalent in training and education in areas such as lean sigma or MBA
- Excellent verbal and written communication skills.
- Self-starter with proven ability to thrive in a fast-paced environment handling multiple simultaneous high priority tasks
- Successful track record of developing and mentoring staff
- Maintains high ethical standards, including a commitment to Vertex's values and behaviors
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Program Manager, Exploratory Development and Lab Solutions |
| Minimum Education Requirements:
? BS/BA in a Science Field ? Chemistry, Biology, etc..
? A degree or related experience in an Information Systems or Computer Science field is a plus
Minimum Experience Requirement:
? Previous experience working in a Pharmaceutical Research environment
? Minimum 5 years defining, implementing, and supporting Research, Discovery and Lab Systems.
? Minimum 5 years in a Project Management role or equivalent role
? Part of an IS team that has been responsible for developing a strong product pipeline
? Consulting experience in working with Research and Discovery or Clinical solutions a plus
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Sr. Systems Analyst-Enterprise ETL |
| ? Languages: SQL, PL/SQL, Java, scripting languages
? Databases: Oracle 11g (preferred), 10g
? OS: Linux, Windows
Preferred technical skills (a plus):
? Enterprise ETL Platform (Talend, Informatica, Datastage)
? Data Warehouse design and modeling (Oracle preferred)
? Master Data Management experience (Siperian preferred)
? Experience with all phases of software development, including requrements, design, development and testing
Technical and Communication Skills:
? Ability to work interactively with users, management and support team.
? Ability to work within established coding and documentation standards
? Team contributor with good communication skills and strong analytical, problem solving skills.
Preferred Education and Experience Levels:
? B.S and 5 years relevant work experience
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Oracle EBS Manager/Lead |
| Necessary technical skills:
? Applications: Oracle E-Business Suite 11i (11.5.10.2),
? Languages: SQL, PL/SQL, Java, scripting languages
? Databases: Oracle 11g
? OS: Linux, Windows
? ETL Tools: Data Loader, SQL*Loader
? Oracle AME
? Use of API?s in data processing following coding standards
Preferred technical skills (a plus):
Developer Tools: Oracle Developer Forms, Oracle Developer Reports, Oracle Discoverer (9i, 10g), Oracle Alerts, Oracle Work flow builder, Noetix Reports, BI Publisher (XML Publisher), Application Desktop Integrator (ADI), Web ADI, Talend Integration Suite
Technical and Communication Skills:
? Expertise in Oracle 11.5.10 financials modules including Oracle General Ledger, Oracle Payables, Oracle Assets, Oracle purchasing, Cash Management, Project Accounting
? Hands on experience with Oracle 11.5.10 HR, OPM, and Supply Chain Management
? Ability to work interactively with users, management and support team.
? Team contributor with good communication skills and strong analytical, problem solving skills.
Preferred Education and Experience Levels:
? B.S and 7 - 10 years relevant work experience
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Associate Director, Phase IV Research |
| ? A bachelor?s degree in the life sciences, business administration or a related field. An advanced degree in health sciences is a plus.
? 3-5 years experience in conducting human clinical trials as part of investigator team and/or pharmaceutical sponsor.
? Familiarity with Good Clinical Practice (GCP) procedures and rules/regulations for conduct of human clinical trials.
? Understanding of the processes required for conduct of IND- and non-IND clinical research, including protocol development, IRB (or Ethics Committee) review, and safety reporting.
? A track record of success functioning in dynamic, matrix environments with the ability to multitask and adapt to rapid changes.
? Exceptional written and verbal communication skills along with the ability to interact constructively across all levels of an organization and with thought leaders and other external collaborators.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Manager, Health Value & Outcomes Research |
| ? A bachelor?s degree in the life sciences, business administration or a related field with a preference for an advanced degree (MD, PharmD, MPH, MS, MHA or MBA). Educational focus in the areas of health economics or outcomes research would be beneficial
? 3 - 5 years of current experience with health economics and outcomes research for the biotechnology or pharmaceutical industries
? Working experience with economic modeling and payer market access tool creation
? Familiarity with payer dossiers, epidemiology, economic analyses, reimbursement and pricing environments
? A track record of success functioning in dynamic, matrix environments with the ability to multitask and adapt to rapid changes
? Exceptional written and verbal communication skills along with the ability to interact constructively across all levels of an organization and with thought leaders and other external collaborators
? The ability to effectively present technical data and complex concepts to diverse audiences
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Finance Manager |
| ? Bachelors degree and 5+ years of relevant work experience; CPA or relevant corporate accounting experience
? Demonstrated strong leadership attributes and ability to successfully drive results
? Project management and process improvement experience with complex operational issues
? Excellent written and oral communication skills with ability to generate concise reports and verbal updates
? Strong interpersonal skills and effective in influencing others
? Demonstrated strong analytical skills
? Strong skills and experience with financial systems (e.g., Oracle/ERP, planning systems)
? Experience with financial management of outsourced services and complex contracts a plus
? Flexibility to work in a fast paced and dynamic work environment
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Director, Business Information |
| MBA, Masters, or relevant advanced degree and 8+ years of relevant work experience. Must have strong leadership skills including prior people management experience.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Head of Medicinal Chemistry |
| Possessing a Ph.D. in medicinal or synthetic chemistry, the Head of Medicinal Chemistry will most likely be currently leading a small to medium size chemistry domain in a large pharmaceutical or biotech company and will meet the following qualifications:
(a) Have a minimum of 10 years experience, as a member of a successful multidisciplinary R&D team in pharmaceutical drug discovery, with a demonstrated track record in the chemical design and synthesis, as well as biological characterization of drug candidates
(b) Have experience in successfully leading and managing a mid-size (minimally 15 scientists) group conducting drug discovery research, including leadership of strategic planning of chemical patent protection, construction and management of spending budgets for researchers.
(c) Possess an expert knowledge in the modern methods of synthetic and medicinal chemistry with proven ability to successfully and simultaneously conduct medicinal chemistry on multiple projects
(d) Possess a strong knowledge of computational chemistry methods and understanding of the target-based taxonomy of drug candidates as well as a solid working knowledge of biophysical methods such as: X-ray crystallography, macromolecular NMR, high-throughput screening as applied to drug discovery, and preferably how scale-up chemistry and formulations development are expedited for development candidates
(e) Command a solid grasp of cellular /molecular biology, biochemistry, disease pharmacology, mechanisms of drug metabolism and molecular toxicology, pharmaco-kinetic and pharmaco-dynamic sciences, and the evaluation of formulations for the in vivo evaluation of drug candidates
The Head of Medicinal Chemistry will be a dynamic and innovative scientist, with a well-developed sense of self-awareness, leadership and independence. Further, he or she will be an inspirational communicator, in written and verbal formats, with the demonstrated ability to instill vision for department, and collaborate effectively with counterparts in diverse domains such as biology, pharmacology, computational sciences and biophysics. As a vital part of Vertex? research management team, he or she will play a critical role in enabling the discovery goals of the research site.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Sr Research Scientist |
| Requirements:
* Ph.D., or equivalent degree
* Post Doctoral Experience preferred
* 5 - 10 years of pharmaceutical industry experience in DMPK
* Experience in GLP regulations
* Demonstrated understanding of drug development process within different therapeutic areas
* Excellent verbal, written and communication skills and project-directed presentation skills
* Working knowledge of drug development process and ICH requirements for drug development
* Successful track record of managing staff, and the ability to operate in a matrix environment
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Sr Scientist, DMPK |
| - Ph.D., or equivalent degree; Post Doctoral Experience is additional qualification.
- 6 - 10 years of Pharmaceutical Industry experience in DMPK
- Experience in GLP regulations, SOPs, interactions with Toxicology, Clinical Pharmacology, Clinical Research, Pharmaceutical Research and Development
- Demonstrated understanding of drug development process within different therapeutic areas
- Good verbal, writing and communication skills and project directed presentation skills
- Working knowledge of drug development process and ICH requirements for drug development
- Established supervisory and ability to operate in a matrix environment
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Commercial Program Manager |
| Minimum requirements include:
· Bachelor?s degree with a preference for an advanced degree and / or a certification in project management
· 5+ years experience in the commercial function of pharmaceutical and/or biotechnology industries
· Experience managing projects related to the launch of pharmaceutical or biotechnology products
· Proven project management skills including the ability to effectively and strategically communicate information and ideas, both written and verbal, to diverse audiences; manage multiple tasks and priorities; adapt to new projects rapidly and to multiple projects effectively; employ good listening skills; build mutual trust and encourage respect and cooperation among team members; inspire loyalty
· Demonstrated ability to work independently and manage projects that require collaboration across functional areas including Customer Outcomes Operations, Marketing, Market Research, Managed Markets, Medical Affairs, Finance, Information Technology and Corporate Learning & Development
· Demonstrated analytical and information technology skills; experience with MS Project or program management systems desirable
· Function as a team player, developing rapport and credibility with key stakeholders
· Display solid ethics and a fit for Vertex?s core values and beliefs
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Scientist I |
| A Ph.D. or Master's or Bachelor's degree in the life or physical sciences with a preference for a concentration in Chemistry, Analytical Chemistry or Pharmaceutical Chemistry
- 0 - 3 years (PhD), 3 - 5 years (MS) or 6+ years (BS) current relative industry experience working in drug substance and drug product support
- Broad awareness of the drug development process, including clinical design, chemical development, and formulation development, especially how those processes impact analytical method development, validation, and method transfer are essential
- Good understanding of GMP and hands-on GMP experience as well as how to develop methods that are GMP friendly are preferred.
- Have received general training/coursework on analytical instruments;
- Working knowledge of analytical instrumentation such as HPLC, GC, UV-VIS, LC-MS, KF, and dissolution apparatus required.; experience with USP IV flow through apparatus a plus.
- Solid experience with HPLC-UV method development preferred.
- Strong capabilities with Excel or other spreadsheet based applications, statistically training a plus.
- The ability to work successfully in both a team/matrix environment as well as independently;
- Familiarity with various sold dosage forms: including tablets, capsules, and solid dispersions is desirable;
- The ability to work in a fast pace environment, manage priorities, and maintain timelines for multiple projects
- Excellent written and verbal communication skills, including familiarity with Scifinder and other journal databases
- Established organizational skills
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Sr. Scientific Associate |
| Preferred Education and Experience:
- A Bachelor's degree in the life sciences or physical sciences with a preference for a concentration in Chemistry, Analytical Chemistry or Pharmaceutical Chemistry with 3-5 years related experience.
- Working understanding of DISSOLUTION, HPLC, LC-MS, GC, GC-MS, FT-IR, UV-VIS, KF, and other instruments used in the analysis of pharmaceutical products
- An interest in and passion for establishing a career in analytical development and the biopharmaceutical industries
- The ability to work successfully in both a team environment as well as independently
- Excellent written and verbal communication skills
- Established organizational skills
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp QA Specialist |
| * B.S (or equivalent degree) and 3-5 years of relevant work experience
* Experience with analytical testing and data review in a GMP environment.
* Experience with the following analytical techniques desirable; HPLC, GC, Dissolution, KF moisture, TGA, FTIR, NMR, UV, wet chemistry. (With emphasis on HPLC and GC experience)
* Reference standard testing.
* Non-conformance or laboratory investigation experience.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Sr. Engineer |
| Job Requirements:
? Minimum 5 years IT experience in an Infrastructure support role specializing in storage management
? Strong technical, analytical, and troubleshooting skills with experience in troubleshooting multi-tier environments
? Excellent communication skills - both written and verbal. Must be able to communicate with all team members, both technical and non-technical
? Self-motivated with strong organizational skills, the ability to juggle multiple high-priority tasks and maintain attention to detail.
? Experience working with teams in different time zones and coordinating duties to coincide with global operational schedules.
? Strong experience working with Enterprise SAN/NAS architecture, protocols, and best practices (EqualLogic, HP, NetApp)
? Solid understanding of storage interface technologies such as iSCSI and Fibre Channel.
? Experience operating in a Brocade SAN fabric environment (certification a plus)
? Proven storage provisioning skills, including disk assignment, and LUN masking
? Working knowledge of Enterprise LAN/WAN network architecture, protocols, and best practices as related to iSCSI (Cisco certification or equivalent a plus)
? Working knowledge of UNIX, Linux and Microsoft Windows Server (certifications a plus)
? Experience with data migration tools: robocopy, richcopy, rsync, dump, tar, etc.
? Experience with Enterprise monitoring systems (Nagios a plus)
? Pharmaceutical & FDA regulated experience a plus, experience supporting a Research environment a plus
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Manager, Research and Development Alliances |
| Minimum Education Requirements:
? BS/BA in a Science, Information Systems or Computer Science
Minimum Experience Requirement:
? Previous experience working in a Pharmaceutical Research and Development environment
? Minimum 7 years business analysis / project management and support of Research, Development and Lab Systems.
? Demonstrated Management Skills in a Research Or Clinical Environment.
? Part of an IS team that has been responsible for developing a strong product pipeline
? Consulting experience in working with Research and Discovery or Clinical solutions a plus
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Scientist I, DMPK/Exploratory Development |
| * Ph.D. or MS in Analytical Chemistry, Biochemistry, Pharmaceutical Science, or a related discipline
* Ph.D with 0 ? 3 years of experience or MS degree with 3 ? 7 years of experience
* Hands on experience in LC/MS operation, maintenance, and use for sample analysis
* Data processing experience using Analyst software
* Experience with Watson LIMS, and familiarity with GLP guidelines
* Possess superior communication and writing skills
* Be a team player and also have the ability to work independently
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Manager, Information Services |
| Technical Attributes and Managerial Skills:
* Strong knowledge of industry best practices associated with IT standards, controls, policies and processes.
* Working knowledge of current IT technologies and government regulations that are applicable to the pharmaceutical industry
* Ability to develop and establish strategic and tactical direction for the GIS organization
* Excellent communication skills (written and verbal)as applied to all levels within the GIS organization.
* Proven ability to lead, facilitate and bring closure to team initiatives and projects.
* Formal process improvement experience and /or Six Sigma certification desired.
* Experience working in a Pharmaceutical Information Technology organization in a leadership position desired.
* Software Asset Management experience desired.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Scientist I |
| Minimum requirements:
- A Ph.D. or Master's or Bachelor's degree in the life or physical sciences with a preference for a concentration in Chemistry, Analytical Chemistry or Pharmaceutical Chemistry
- 0 - 3 years (PhD), 3 - 5 years (MS) or 6+ years (BS) current relative industry experience working in drug substance and drug product support
- Broad awareness of the drug development process, including clinical design, chemical development, and formulation development, especially how those processes impact analytical method development, validation, and method transfer are essential
- Good understanding of ICH and FDA method validation guidelines are essential. The ability of identifying areas overlooked in the guidelines is preferred.
- Good understanding of GMP and hands-on GMP experience as well as how to develop methods that are GMP friendly are preferred.
- Working knowledge of analytical instrumentation such as HPLC, GC, UV-VIS, LC-MS, KF, and dissolution apparatus required.; experience with USP IV flow through apparatus a plus.
-Solid experience with HPLC-UV method development preferred.
- Strong capabilities with Excel or other spreadsheet based applications, statistically training a plus.
- The ability to work successfully in both a team/matrix environment as well as independently;
- Familiarity with various sold dosage forms: including tablets, capsules, and solid dispersions is desirable;
- The ability to work in a fast pace environment, manage priorities, and maintain timelines for multiple projects
- Excellent written and verbal communication skills, including familiarity with Scifinder and other journal databases
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
|
| Minimum Requirements Education / Experience:
* Minimum 3-5 years experience in Accounts Payable
* Oracle AP experience is preferred
* Exceptional communication, interpersonal and high level of organizational skills
* Ability to manage time lines and deliverables
* Strong customer service expertise.
* Proficient knowldge of Microsoft Office suite of products
* Ability to be flexible and work in dynamic, fast-paced environment managing multiple tasks
* Ability/experience working with employees at all levels in the organization and across all functions
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Sr. QA Specialist |
| PREFERRED EDUCATION AND EXPERIENCE:
* M.S. (or equivalent degree) and 0 ? 3 years of relevant work experience, or
* B.S. in a scientific or allied health field (or equivalent degree) and 5 ? 8 years of relevant work experience
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Staff Accountant |
| Education:
BS with a major in Accounting, CPA, MBA preferred
Experience:
One to three years experience in an accounting environment, preferably within a pharmaceutical company.
Preferred Skills/Qualifications:
Microsoft suite of software (Excel, Word, etc..).
Experience with Oracle Financial Software a plus
Skills/Competencies:
Excellent communication and organizational skills.
Ability to work independently with strong attention to accuracy and detail
Other Skills:
Ability to communicate effectively with higher levels of management.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Director, Health Value & Outcomes Research |
| ? Advanced degree (MD, PharmD, MPH, MS, MHA or MBA) and an educational or work experience focus in the areas of health economics and outcomes research.
? At least six years of health economics and outcomes research experience in the biotechnology or pharmaceutical industries, including experience with economic modeling, creating market access tools for payers, and managing cross-functional working teams
? Understanding the purpose, content/format, and utilization of AMCP and global value dossiers for formulary and/or reimbursement submission.
? Excellent knowledge of global pricing and reimbursement environment and the requirements of health technology assessment agencies.
? Demonstrated expertise in design and execution of outcomes research and economic analyses.
? Experience with assessment and utilization of available patient reported outcomes instruments in a variety of disease areas. Development and validation of PRO instruments a plus.
? Direct and successful interactions with regulatory authorities regarding PROs and outcomes research preferred.
? A track record of success functioning in a dynamic matrix environment with the ability to multitask and adapt to rapid changes seamlessly.
? Exceptional written and verbal communication skills along with the ability to interact constructively across all levels of an organization and with thought leaders and other external collaborators and customers.
? The ability to effectively present technical data and complex concepts to diverse audiences.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Director, Alliance Management |
| An MBA and/or PhD preferred or equivalent experience, he/she will have at least 7-10 years experience in the pharmaceutical industry with first hand experience in the management of a successful alliance (preferable an alliance that resulted in the launch of a new product).
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Clinical Outsourcing Manager |
| · Bachelor's degree is required
· Life sciences or business experience is preferred
· Minimum of 3 years experience in clinical development including knowledge of contract law and budgets
· Negotiation, organizational and communication skills are required
· Previous experience with clinical trial site agreements is a plus
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Sr. Director, Clinical Epidemiology |
| -M.D. or PhD. in Epidemiology required, as well as formal training in epidemiology
8+ years of pharmaceutical pharmacovigilance experience or equivalent in the field of clinical epidemiology
-Solid knowledge of general medicine and clinical practice evidenced by medical training and/or medical practice experience or designing/conducting clinical epidemiological trials.
-Highly evolved understanding of pharmacovigilance guidelines and regulations
-Effectively interacts with Senior Management and integrates activities successfully across the organization
-Excellent verbal and written communication skills
-Strong leadership skills and experience working in a matrix environment
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Associate Director, Treasury |
| Skills Needed:
* 5-8 years experience in an internal treasury environment
* BS degree, preferably in Accounting, Finance, or Economics
* CTP designation preferred
* Initiative
* Business operations thinking
* Negotiation skills
* Comfortable talking with varied audiences both known and unknown entities
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Contracts Paralegal |
| Qualified candidates should have a minimum of 1 ? 3 years experience in a corporate legal department (in-house or within a law firm) working primarily in contracts. Must possess high attention to detail, strong work ethic, be able to take initiative, and have excellent time management and follow-through skills. A strong ability to engage others at various levels within the Company in a cooperative and collaborative manner along with solid written and oral communication skills are highly valued in this position. Paralegal Certificate and BA or higher required. Experience with Commercial contracts within the pharmaceutical industry is a plus.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Safety Medical Director |
| M.D. required; 3+ years of
pharmaceutical pharmacovigilance experience, ideally both pre- and
post-marketing.
- Solid knowledge of general medicine and clinical practice, evidenced by
medical training and/or medical practice experience.
- Strong leadership skills, as well as experience working in a matrix
environment.
- Must have a strong working knowledge of FDA regulations/ICH guidelines
- Must be experienced in safety reviews of IBs, protocols, final clinical study
reports, and summaries of safety.
- Advanced ability to read, analyze and interpret clinical data and information
- Possess very strong writing skills and advanced verbal communication and
presentation skills.
- Requires strong attention to detail in writing and/or proofing materials
- Ability to work in a fast paced environment with demonstrated ability to
simultaneously manage multiple competing tasks and demands.
- Ability to work independently, take initiative and complete tasks to
deadlines.
- Occasional domestic and international travel may be required (
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Sr Scientist, Commercial Support, QbD and CMC |
| * Education and experience related to organic analytical chemistry (Ph.D. degree with three to five years experience or a Masters degree with ten years extensive pharmaceutical industry experience)
* At least 2 years of practical experience in analysis of small organic molecules with HPLC-MS
* Very good team-working skills and the capability to work in a complex environment
* Efficient organization and good documentation skills
* Good command of English; excellent presentation and report writing skills.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Director, Brand Protection & Investigations |
| A minimum of a Bachelor?s degree in a related field is required. A minimum of 10 years relevant business experience and 7 years experience in a supervisory role are required. Experience in some of the following disciplines: operations, security, competitive intelligence, channel monitoring/investigations, contracts/price monitoring, criminal investigative work, and enforcement and compliance programs, with multi-functional experience is preferred. Healthcare experience is required, while medical device and/or pharmaceutical industry experience is preferred. Prior experience with diversion and counterfeit controls is required. Experience establishing and executing market monitoring and purchase programs is preferred. Must have communication and influential skills to work within a decentralized structure. Must be able to work within and understand a global cultural environment. Negotiation experience required. Relationship building and project management skills are required. Superior communication skill, written and oral is required. Adept understanding of key relevant business processes such as financial systems of distributors, hospitals, and manufacturers, healthcare contacting processes, and supply chain strategies is preferred. Secondary market (gray market) functioning is preferred.
The successful candidate should anticipate 25% of their time would involve international and domestic travel.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Lead Systems Analyst-JAVA |
| Prerequisites:
5+ years Java experience
Java Swing expertise
Comfort with multiple types of RDBMS (Oracle and MySQL preferred)
Strong communication and organization skills
Nice to have's include
Experience in the pharmaceutical industry
Understanding of chemistry/cheminformatics
Knowledge of C++
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Director, Health Economics |
| - Bachelor?s degree in the sciences with a preference for a graduate level degree in a related field of study (e.g. PharmD, PhD, MD, MPH)
- Minimum of 6 years of relevant experience in health economics, and/or pricing functions
- 4+ years of managing or leading project teams is preferred, experience in developing and managing teams and working in cross functional environment is essential
- Health care industry experience and in-depth knowledge of the pharmaceutical business including R&D, clinical and marketing, as well as a good understanding of managed care;
Related therapeutic experience is preferred, specialty pharmacy category (e.g. HIV, MS, Oncology, etc.) experience considered a plus
- Experience in developing innovative communication strategies and tools to support brand and/or disease value propositions is essential. Experience in developing and/ or utilizing HE tools is preferred
- Excellent interpersonal skills are required as is the ability to understand and respond to multiple internal and external customer requests and manage conflict constructively with minimal supervisory support required
- Experience in preparing or reviewing materials for drug formularies considered a plus
- Ability to travel up to 20%
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Labeling Manager, Regulatory Affairs |
| * Bachelor?s degree (preferably in a life sciences field)
* Three to five years of relevant experience in Regulatory Affairs in the area of labeling development and review
* A strong knowledge of US and ex-US technical labeling aspects such as SPL/PIM, PLR, the basic printing process, and regulatory barcode requirements
* Possesses excellent written and verbal communication skills
* Excellent organizational, analytical, problem-solving, proofreading, and decision-making skills
* Strong computer skills, including a working familiarity with electronic document management systems for compliant maintenance and version control of submitted, approved and in-use labeling.
* Working knowledge of regulations, guidelines and precedents related to pharmaceutical product development and marketing, with focus in the area of product labeling and packaging
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Medical Information Specialist |
| * PharmD with on-the-job medical writing experience required
· One to two years experience in the pharmaceutical industry desired
· Ability to manage multiple assignment simultaneously, work independently
· Requires initiative and the ability to maintain a high level of productivity with minimal supervision
· Excellent ability in searching medical literature, interpret and present scientific/clinical trial data and understand statistical analyses
· Expertise in Microsoft Word is required
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Quality Specialist, Quality Systems |
| * B.S. in a scientific or allied health field (or equivalent degree) and 3 ? 5 years of relevant work experience
* Has provide Instructor-led training on various GxP topics as needed
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Manager, Information & Records Management |
| * B.S. in Life Sciences or Library Science (or equivalent degree) and 5 ? 8 years of relevant work experience
* Prior experience as a manager and expertise in GCP/GLP documentation practices and 21 CFR Part 11
* EDMS / Documentum experience preferred
* Basic knowledge of global regulatory submission and clinical TMF documentation and demonstrate strong communication skills and be able to lead others in a changing environment
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Clinical Pharmacology Associate |
| * Bachelor?s degree in quantitative discipline or biological sciences with significant courses in quantitative area.
* Must have some programming skills (preferably in SAS/Splus).
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Clinical Safety Specialist |
| * B.S. (or equivalent degree) and 3 ? 5 years of relevant work experience, or
* PharmD, M.S.N (or equivalent degree) and 1 ? 4 years of relevant work experience
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Manager, Medical Coding, Clinical Data Management |
| * M.S. and 8+ year of relevant experience or a B.S. with 10+ years of relevant experience
* Must demonstrate relevant industry experience, with clear understanding of Medical Coding for Clinical data.
* Demonstrated track record of achieving results in related operations
* Proficiency with medical coding, reporting, and EDC tools, such as dsNavigator, Central Coding, InForm, J-Review
* Strong working knowledge of applicable regulations and industry trends
* Experience in demonstrating leadership, influence and collaboration in a matrix-managed environment
* Solid management experience and the ability to hire and develop staff, as well as leverage resources from within function
* Strong consultative, listening and analytical skills
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Senior Clinical Pharmacologist |
| * PharmD or Ph.D. and 2-5 years of industry experience
* NCE drug development experience with at least 5 NCEs in the past
* Possesses good knowledge of drug Development Programs and a keen awareness of development issues
* Able to integrate the activities of distinct functional groups across multiple projects
* Can recognize and carry out productive new development initiatives/directions Is a mid-level experienced mentor who effectively infuses confidence and team commitment: can make clear written and oral presentations.
* Exhibits a record of excellent operational and ethical standards, and team-improvement
* Demonstrated ability to provide career development to staff
* Able to recognize and resolve important organizational problems and/or infusing innovation Has leadership abilities, can initiate and carry out tasks with little direct supervision
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Manager, Global Trial Activation (GTAG) |
| * Experience and skills leading inter-departmental projects
* Proactively seeks out and recommends process improvements
* Proven track record of anticipating potential study start-up problems and preparing contingency plans as needed
* Communicates clearly and precisely with all levels of the company
* Demonstrated management skills for individual and team development.
* Understanding and experience with global regulatory environment, strong working knowledge of ICH/GCP guidelins; Bachelor?s degree required, advanced degree preferred, with 7+ years of relevant industry experience
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Safety Database Applications Specialist, Global Patient Safety |
| * A bachelor?s degree in a technical discipline or a technical degree.
* A minimum of 1 year hands-on analysis and application support experience in a Windows O/S application environment supporting multi-tiered application architecture to include web based application clients.
* Approximately 1 year experience in drug safety and/or data management with knowledge and experience with ARISg, or a comparable commercial safety database/system, including configuration/operational support.
* Familiarity with GCP, FDA, EMEA regulatory requirements as they apply to pharmacovigilance and drug safety and working knowledge of database design and system life-cycle concepts.
* Familiarity with Signal Detection tools (Empirica, Multi-item gamma Poisson (MGPS), etc)
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Sr. Statistical Programmer |
| Experienced with all SAS language, procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH.
Experienced with the CDISC SDTM and AdaM models and transforming raw data into these standards.
Experienced working with all types of safety data and coding dictionaries (MedDRA and WHODRL) commonly used by the pharmaceutical industry.
Experienced working in a team environment providing technical leadership and solving clinical trial reporting problems of moderate to high complexity within budget and customary time line constraints while assuring high quality standards.
Skilled at performing quality control checks of SAS code and output produced by other Statistical Programmers.
Knowledgeable regarding software validation and system development life cycle concepts.
B.S. in Biostatistics, Statistics, Computer Science, or a related field and a minimum of 5 years of SAS and relevant pharmaceutical industry experience.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Manager, Stock Plan Administration |
| Requirements:
* Bachelors Degree in Accounting, Finance, or equivalent experience
* Experience with global multinational employer issuing multiple stock programs and designs, preferable through Equity Edge system.
* CEP (Certified Equity Professional) certification preferred
* Knowledge of Section 16
* Knowledge of U.S. accounting, legal, disclosure and tax issues
* Familiarity with non-U.S. tax, securities, and legal issues pertaining to stock plans
* Demonstrated client focus and ability to build relationships and trust with various groups
* Knowledge of Microsoft suite of applications, stock plan administration software, etc.
* Excellent communication skills, both oral and written
* Strong attention to detail to review and validate the accuracy of information
* Experience with or working knowledge of multiple stock plan vendors and third party administrators preferred
* Ability to work with hands-on involvement as well as act as mentor/coach and set direction
* Contribute individually with minimal supervision within a team oriented environment
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Associate Marketing Director |
| Ideal experience and skills match:
· A Bachelor's degree in marketing, business or a science discipline. An MBA is an preferred, but not required
· At least 8 years experience in the specialty pharmaceutical and/or biotech industries; comprised of at least 5 years marketing, demonstrating progression of responsibility.
· Global marketing experience required
· Launch experience required; Orphan drug launch preferred
· Demonstrated strategic planning, communication and presentation skills
· Demonstrated ability to develop solutions to complex problems with creativity and innovation
· Proven teamwork in small teams, leadership and collaboration skills, with a demonstrated ability to influence at all levels of business
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
|
| - Red Hat Linux 5.5 64-bit
- JBoss 5.1 and JBoss EAP 5.0
- Oracle 10g (10.2.0.4)
- Cognos Business Intelligence Server 8.4.1
- Cognos Business Intelligence Modeling 8.4.1
- Understanding of EDI and data integrations with iMANY
- Use of API?s in data processing following coding standards
Preferred Education and Experience Levels:
- M.S and 3 ? 5 years relevant work experience, or
- B.S and 5 ? 7 years relevant work experience
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Staffing Assistant |
| * Bachelor?s degree or equivalent required.
* 0-4 years experience working on a fast-paced, high-volume HR team, or several years in a fast-paced administrative environment.
* Exceptional organizational and communication skills, and computer proficiency in MS Office and/or Lotus Notes required.
* Applicants must be able to manage multiple tasks and address issues with a sense of urgency, handle sensitive situations and confidential materials with tact, and challenge conventional practices by introducing new ideas and process improvements.
* Must be able to interact and communicate effectively with all levels in and outside the organization and demonstrate a strong customer service.
* Strong team players and those with high attention to detail are urged to apply.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Clinical Staffing Consultant |
| Minimum Requirements
· 5+ years pharmaceutical clinical or medical recruiting experience a must, minimum of a Bachelors degree or equivalent
· Experience working in a fast-paced, highly matrix organization
· Proven track record of finding unique ways to source and attract qualified candidates
· Superior selection skills and a high level of proficiency in assessing individuals
· Proven ability cultivating successful relationships internally and externally
· Results driven, ability to demonstrate/quantify success relative to established targets and metrics
· Strong listening, facilitation and communications skills
· Strong organizational, multi-tasking and computer and web skills, along with the ability to handle sensitive and confidential situations/information
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Director, Clinical Operations |
| * Global experience within all phases of drug development with advanced understanding of other functions; including but not limited to: Research, Non-Clinical, Supply Chain, Commercial, Regulatory and Medical Affairs
* Experience in strategic planning, business process improvement and achieving results.
* Experience in demonstrating leadership and influence and collaboration in a matrix environment
* Application of Project Management tools, methodologies, practices, risk analysis, decision analysis and contingency planning
* The ability to effectively communicate with Clinical Leadership and Clinical Project Managers
* Strong consultative, listening and analytical skills
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company?s strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex?s product pipeline is focused on viral diseases, inflammation, autoimmune diseases, cancer, pain and bacterial infection.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Director, Clinical Site Services |
| * Bachelor?s degree required, advanced degree preferred ,with 7+ years of relevant industry experience
* Extensive experience strategizing and implementing global study execution activities
* Extensive experience strategizing and implementing global study execution activities
* Ability to thrive in a fast-paced, evolving environment with experience in a matrix organization
* Excellent verbal and written communication skills, superb oral presentation skills
* Ability to thrive in a fast-paced, evolving environment with experience in a matrix organization
* Solid working knowledge of ICH/GCP guidelines
* Successful track record managing direct reports and contractors
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Lead Engineer |
| Job Requirements:
? A minimum of 8 years experience with CommVault (Enterprise Backup System) backing up servers, databases, SAN and NAS Storage.
? Strong knowledge of Enterprise Tape Libraries (Quantum a plus) and LTO-X technologies.
? Linux administrative experience (RedHat 5.x a plus)
? Windows administrative experience (Windows 2008 a plus)
? Basic networking skills
? Ability to function effectively in a fast-paced environment, handles multiple tasks simultaneously, and meets deadlines.
? 5+ years experience in a 700+ server environment across multiple sites
? Excellent communication skills both written and verbal
? Self-motivated with outstanding troubleshooting experience
? Research, Pharmaceutical & FDA regulated experience a plus
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The company's strategy is to commercialize its products bother independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, inflammation, autoimmune diseases, cancer, pain and bacterial infection.
Vertex Pharmaceuticals |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| VP, Market Research |
| The ideal candidate is currently leading market research in a fast-moving consumer goods company or a consumer based health company. It is important that the individual be well versed in research methodology, understand the use of research tools and possess the ability to apply them to solve the company?s business problems. The individual must be a team player, have excellent communication skills, and must have proven leadership abilities.
People Leadership Skills: Successful candidate needs to be capable of leading and developing a strong team of capable Market Research associates. This includes driving results, empowering teams, building processes, managing performance and developing future leaders.
Strategic Marketing Skills: The successful candidate will have demonstrated the ability to identify unmet consumer needs and use consumer knowledge to evolve services and create effective marketing strategies. This person will have a demonstrable record of standing in the end-users shoes, and motivating behavioral change one step at a time.
?Excellent Analytical Acumen: The successful candidate will have demonstrated the ability to assess disparate data streams and distill them into meaningful and, ultimately, actionable strategic recommendations. This encompasses consumer, constituent and competitive environments. A track record of identifying profitable consumer segments and separating those from unprofitable ones is a necessity. Identifying competitor?s intent before they take action is required.
?New Product Concept Development: This person will have a record developing new product concepts from fact-based analysis with a strong end-user orientation. He or she will have worked closely with technical product development teams to actualize the product.
?End-Consumer Orientation: The information resources are highly targeted due to the well-defined target audience. Therefore, the successful candidate will have extensive success with highly customized research protocols, and not be as reliant on broad-based psycho/demo-graphic studies. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| VP, Global Purchasing |
| 10+ years of Procurement experience, 3+ years in the healthcare industry or equivalent. Significant leadership experience, extensive experience in terms of leading and developing teams within a matrix organization and across geographies and cultures. Extensive experience change and category management.
Bachelor?s degree required at a minimum, master?s degree preferred; in fields such as business administration, finance, law or a scientific or technical field. Strong preference for CIPS or similar professional qualification. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Traning Solution Partner (Development) |
| Masters Degree (or adequate) preferred, candidates with previous working experience in pharmaceutical industry preferred; 5+ years HR/Training experience required; scientific education is an additional advantage.
Fluent in English, other languages are an additional advantage. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Training Manager, Reclast |
| ? Bachelor?s degree
? Strong written, oral communication skills
? Extensive therapeutic experience,
? 3-4 years of pharmaceutical sales experience
? Strong clinical & Therapeutic knowledge
? Brand strategy, tactics understanding
? Partnering Skills (brand, medical, PRC, vendors etc)
? Presentation and platform skills. Ability to communicate in small and large settings
? Knowledge of field /sales force (key client knowledge)
? Administrative management skills - planning, organization, operational decision making and analysis.
? Creativity and innovation.
? Thorough knowledge of pharma industry, Novartis products and competition.
? Ability to manage multiple projects
? Fluent English (oral and written) |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Trade Analyst ? USMM Trade Operations |
| BS/BA degree required.
Minimum of 2-4 years of analytical experience.
Must have at least 2 years in the pharmaceutical industry specifically in trade operations, sales and distribution or customer support.
Strong working knowledge of SAP, Sales and Distribution module and Business Warehouse.
Preferred experience of reporting within SAP
Good problem solving, decision, verbal and written skills
Effective interpersonal and organizational skills
Must have the ability to plan and organize work with multiple priorities.
Computer literacy is required, Microsoft Office, Excel, Word, PowerPoint, and Access
Strong working knowledge of DEA & FDA regulations |
| Novartis Oncology |
na |
DC |
9/4/2010
|
| Territory Sales Representative- Washington, DC |
| Minimum Experience Required:
2-4 years successful outside sales experience in a business-to-business selling model.
Preferred Level:
A combination of business-to-business selling experience, at least One (1) year contact lens sales/ophthalmic related sales/contact fitting experience, and/or medical sales experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel also required. Must successfully complete our "New Hire Sales Training Program".
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
NV |
9/4/2010
|
| Territory Sales Representative- Las Vegas North/Reno |
| Minimum Education Required:
Bachelor's degree or equivalent
Minimum Experience Required:
2-4 years successful outside sales experience in a business-to-business selling model.
Preferred Level:
A combination of business-to-business selling experience, at least One (1) year contact lens sales/ophthalmic related sales/contact fitting experience, and/or medical sales experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel also required. Must successfully complete our "New Hire Sales Training Program".
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
KY |
9/4/2010
|
| Territory Sales Representative- Bowling Green, KY |
| Minimum Education Required:
Bachelor's degree or equivalent
Minimum Experience Required:
2-4 years successful outside sales experience
Preferred Level:
One (1) year contact lens sales/ophthalmic related sales/contact fitting experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel also required.
Must successfully complete our "New Hire Sales Training Program".
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
VA |
9/4/2010
|
| Territory Sales Representative Virginia Beach, VA |
| Minimum Education Required:
Bachelor's degree or equivalent
Minimum Experience Required:
2-4 years successful outside sales experience in a business-to-business selling model.
Preferred Level:
A combination of business-to-business selling experience, at least One (1) year contact lens sales/ophthalmic related sales/contact fitting experience, and/or medical sales experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel also required. Must successfully complete our "New Hire Sales Training Program".
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Territory Sales Representative Johnstown, PA |
| Minimum Education Required:
Bachelor's degree or equivalent
Minimum Experience Required:
2-4 years successful outside sales experience in a business-to-business selling model.
Preferred Level:
A combination of business-to-business selling experience, at least One (1) year contact lens sales/ophthalmic related sales/contact fitting experience, and/or medical sales experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel also required. Must successfully complete our "New Hire Sales Training Program".
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
MO |
9/4/2010
|
| Territory Sales Representative - St. Louis, MO |
| Minimum Education Required:
Bachelor's degree or equivalent
Minimum Experience Required:
2-4 years successful outside sales experience in a business-to-business selling model.
Preferred Level:
A combination of business-to-business selling experience, at least One (1) year contact lens sales/ophthalmic related sales/contact fitting experience, and/or medical sales experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel also required. Must successfully complete our "New Hire Sales Training Program".
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
NC |
9/4/2010
|
| Temporary HR/Compensation Analyst |
| Education : Bachelors degree
Experience: 1-3 yrs of Compensation/Benefits and/or Generalist experience, preferably Peoplesoft and SAP experience. Ability to manage sensitive employee information in a confidential manner. |
| Novartis Oncology |
na |
CO |
9/4/2010
|
| Technical Services Scientist |
| ? BS degree required (Engineering or Pharmacy is preferred)
? 6 years related experience with BS Degree
?4 years related experience with MS Degree
? 2 years related experience with PhD Degree
Competencies:
?Technical Competence
? Solid Knowledge of cGMP and FDA regulations and guidelines
? Good Written and Verbal Communication Skills
?Speed/Action/Simplicity/Initiative |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Team Leader II, ARD |
| PhD, Chemistry or closely related scientific field, with 3-5 years of related pharmaceutical experience. MS, Chemistry or closely related scientific field, with 5-7 years related pharmaceutical experience. BS, Chemistry or closely related scientific field, with 7-10 years related pharmaceutical experience. Minimum of 2-4+ years previous and demonstrated supervisory experience. |
| Novartis Oncology |
na |
CO |
9/4/2010
|
| Supervisor, Production - 3rd Shift |
| ? BA/BS and 4 plus years of professional related experience or Associate Degree or technical degree equivalent and 6 plus years of related experience
? Supervisory experience in a production environment preferred
? Technical training of pharmaceutical processes and equipment
? Proficiency in operation and trouble-shooting of the packaging/production equipment preferred
? Knowledge of general process improvement theory, customer service practices, coaching and counseling approaches, and conflict management techniques.
? Ability to write equipment and operation procedures and review, assess and write technical reports
? Ability to handle compliance issues with a sense of urgency and accuracy
? Strong Customer/Quality focus
? Strong written and verbal communication skills
? Results oriented
? Demonstrated ability to apply Lean/6 Sigma concepts and to identify continuous improvements to increase equipment efficiency |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Study Support Associate II |
| ? 2-year degree in Veterinary Sciences or related animal management field, 4-year Science degree, or an equivalent amount of prior experience required.
? Thorough understanding and comprehension of operational facts, techniques, nomenclature, equipment, theories, etc. as they relate specifically to job performance and function in the laboratory animal research environment.
? Certified Veterinary Technician (CVT), AALAS LAT/LATg, and/or similar certification required.
Strong communication skills
Minimum 3 - 5 years experience in a technical skills tract laboratory animal program required. Weekend work will be required. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Study Support Associate I |
| BS/MS in biomedical science, pharmacology, or related discipline. Hands-on experience with animal models is essential, and the selected candidate should also have experience in virology and/or bacteriology is preferable. An understanding of pharmacokinetics is desirable. The candidate should also have experience in experimental design, animal surgery, microbiology techniques, data interpretation, and statistical analysis. A strong work ethic, excellent oral and written communication skills, and the ability to function in an interdisciplinary team are essential. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Study Support Associate I |
| ? 2-year degree in Veterinary Sciences or related animal management field, 4-year Science degree, or an equivalent amount of prior experience required.
? Thorough understanding and comprehension of operational facts, techniques, nomenclature, equipment, theories, etc. as they relate specifically to job performance and function in the laboratory animal research environment.
? Certified Veterinary Technician (CVT), AALAS LAT/LATg, and/or similar certification required.
Strong communication skills
Minimum 3 - 5 years experience in a technical skills tract laboratory animal program required. Weekend work will be required. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Strategic Alliances Negotiator |
| Minimum requirements An Bachelor?s or Master?s Degree is a scientific area is desired, as is either an MBA or a JD, the Strategic Alliances Negotiator will possess an excellent in-depth
knowledge of the pharma/biotech arena, and will
have at least five years experience in a licensing or business development role. He or she will have a demonstrated capability for completing high quality transactions.
Experienced in partnering with biotechnology companies and/or academic/research institutions, he
or she will possess superior analytical, strategic and
communication skills. Well organized, detail oriented,
with a strong sense of urgency, the Negotiator will be a
team player comfortable working in a global matrix
system. A creative thinker, he or she will establish
innovative business solutions and concepts with a
strong strategic vision, consensus building talent,
negotiation skills, and a strong entrepreneurial spirit.
Considered reliable, pro-active, hands-on, able to
manage projects and function with autonomy, he or
she will understand how to influence people and
situations in an R&D setting. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr. Scientist, Research |
| 9-13 Years with Bachelors of Science, 7-11 Years with Master of Science, 4-8 Years with PhD. |
| Novartis Oncology |
na |
CO |
9/4/2010
|
| Sr. Scientist, Process Development |
| Experience & Education
9-13 years with Bachelors Degree, 7-11 years with Master's Science, 4-8 years with PhD |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Sr. Project Manager, IT Technology |
| BS or advanced Education in Information Technology or Computer Science
? Demostrated high level of creativity with respect to utilization of core Project Management practices focused on successful project delivery not the process
? Successfully delivered high visibility projects
? Has strong communication and collaboration skills, successfully resolves conflict
? Has strong leadership skills and demonstrated ability to motivate a global, intra-discipline project team
? Demonstrated ability to work in a weak matrix organization
? Effectively uses Project Management tools to facilitate decision making and enhance communication
? Has a proactive and practical approach to project delivery
? Demonstrated ability to successfully work with vendors
? Understands IT Service-based organizational models, roles and metrics
? Has working knowledge in the area of IT service delivery
? Understands basic concepts of Infrastructure architecture
? Understands concepts and challenges of IT service outsourcing |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Sr. Investigator, Global Imaging/MRI |
| The ideal candidate will have a PhD with a minimum of 2-4 years experience (although greater experience is deemed an asset) within industry/academia in the following areas:
- Small animal MRI experience (preferably on Bruker systems) may include multimodality imaging
- Extensive knowledge of imaging application
- Animal skills, such as handling, restraining, anesthesia and injections (IP, IM, IV) in rodents and rabbits.
- Proficiency in data analysis using Excel and statistical software, image processing; computer proficiency (e.g. C++, Matlab, IDL, Linux) is a plus.
- Good inter-personal, communication skills, and working with diverse and talented scientific teams. |
| Novartis Oncology |
na |
CA |
9/4/2010
|
| Sr. Document Controller - Vacaville, CA |
| High school diploma or equivalent
4 years experience in technical word processing or business college certification and 2 years experience. Knowledge of Good Manufacturing Practice (GMPs) required |
| Novartis Oncology |
na |
NC |
9/4/2010
|
| Sr. Director, Operations |
| Skills and Knowledge: Direct experience in Engineering, Manufacturing, QA, Packaging, Production Planning, and Process Development, as well as Logistics and Technical Services; A proven track record of introducing new technology into site operations for continuous improvement in operations, cost management, organizational development, cycle time and capital projects planning and management; Effective team player who possesses strong communication skills. Good communication skills, be articulate and clearly have presence; Mentoring and counseling experience. Team based in thinking with an inclusive management style; Sense of urgency as to objectives, timelines and milestones. Additionally, a contagious make-it-happen approach to the achievement of results; Proven problem solving skills and a roll-up-the-sleeves attitude in working with peers, cohorts and subordinates; Strong financial skills to develop and manage Operations and Facilities budgets; Strong team leadership skills including strong evidence of cross-functional leadership.
?
Education: BA/BS (Technical Emphasis ? Science / Engineering) degree is required; MS or MBA is preferred, but not required. Work Experience: 15 + years of Pharmaceutical Manufacturing experience; Minimum 12 years experience in formulation pharmaceutical manufacturing. Additionally, 10 + years in a senior operations leadership role; Must have demonstrated substantial cGMP knowledge and FDA regulatory inspection experience. |
| Novartis Oncology |
na |
CA |
9/4/2010
|
| Sr. Auto & Controls Engineer |
| ? Requires a Bachelors degree in an engineering or related discipline. Equivalent experience may be accepted.
? Requires a minimum of 8 years industry work experience.
? Must be very comfortable with 21 CFR Part 11 and GAMP.
? Must have 5 years experience in a GMP pharmaceutical manufacturing environment or other regulated environment.
? Experience with computer-assisted engineering and design software, CAD and graphics skills are a plus.
? Batch processing and/or filling/packaging controls experience are a must.
? BMS experience is a plus.
? Must possess sound technical judgment and use structured decision-making techniques.
? Good oral and written communication skills are a must.
? Strong computer skills are required.
? Must have an ability to provide technical engineering support in a collaborative, team-oriented project environment.
? Strong project management skills are required.
? Project management skills are a plus. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Statistical Programmer |
| BA/BS or equivalent experience in mathematics, statistics, computer science or life sciences or related field,
- Fluent in English (oral and written)
Intermediate knowledge of and experience with SAS software.
- Working knowledge of database design/structures.
- Good understanding of global clinical trial practices, procedures, methodologies.
- Good understanding of regulatory requirements relevant to SR (e.g, GCP, ICH).
- Intermediate knowledge of office tools.
- At least 4 years experience in a programming role preferably supporting clinical trials and/or in the pharmaceutical industry (2 years for MS Statistics/Computer Science graduates). |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Sr Scientist, Protein & Toxicology Lab (non PhD role) |
| Minimum Requirements
? Education: Bachelor or Master Degree in Chemistry, Biochemistry, Physiology, Cell Biology, Toxicology or a related Biological Science, with 5+ years of academic or industrial experience in with significant experience in protein mass spectrometry.
? Extensive hands-on experience in the protein biochemistry methods, such as HPLC/Bioplex/gel electrophoresis/cell culture methods etc. Hands-on experience with peptide LC/MS/MS analysis is a great plus.
? Expertise in one or more of the following areas would be an advantage: protein detection assays; functional analysis of proteins in mammalian cells; purification of native and recombinant proteins; protein-protein and protein-ligand binding studies, knowledge of toxicology or cell biology
? Fluency in English (written and spoken).
? Flexibility and ability to work in a team, comfortable with multitasking, good written and oral communication skills, independent and accurate working style, ability to plan and organise effectively, willingness to take on additional responsibilities are expected. |
| Novartis Oncology |
na |
NE |
9/4/2010
|
| Sr Process Engineer |
| Required: BS degree in an appropriate scientific, pharmaceutical or engineering discipline and atleast 7 to 10 years of demonstrated experience in pharmaceutical formulation, packaging engineering, and/or process development. Experience with pharmaceutical production practices, manufacturing and packaging equipment, and instrumentation and controls. Working knowledge of GxPs. Demonstrated ability to execute facility, process, computerized system, cleaning, and equipment validations.
Preferred: Packaging Engineer or Electrical Engineer with advanced degree. Prior accomplishments in pharmaceutical formulation, development for various dosage forms, or packaging engineering in relevant environments. Prior experience executing capital projects. Working knowledge of analytical testing preferred; demonstrated experience with quality engineering methodology desired.
Only on-line resumes will be accepted. If you require accommodation under the American?s with Disabilities Act to apply for this position,contact Suzanne Drew at (402) 467-8808. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Principal Biostatistician |
| At least Masters Degree in Statistics (or equivalent degree) with 5 years of experience or PhD with 2-3 years of experience.
Fluent English (oral or written)
1. Experience in all tasks of a Trial Statistician.
2. Proven knowledge in Statistics and its applications to clinical trials.
3. Proven knowledge of drug development and HA guidelines. Background medical knowledge, preferably in relation to the specific therapeutic area.
4. Proven knowledge of statistical software packages.
5. Good communication and presentation skills.
6. Good team player. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Sr Pharmaceutical Counsel |
| Key Requirements:
A) Educational
? JD or LLB Degree and admission to the Bar in at least one U.S. state, or an equivalent admission in a relevant foreign jurisdiction
B) Experience
? 10+ years of experience in legal practice
o minimum of 5 years at a law firm required
o experience in management of HR issues, including litigation
o in-house experience preferable
C) Specialized Skills and Knowledge
? Strong knowledge of HR law and issue management, including dispute resolution and litigation
? Clear communication skills, written and oral
? Ability to translate complex legal principles to management
? Demonstrated good ?bed-side manner? in handling sensitive employment issues
? Ability to contribute in a team context
? Strong interpersonal skills in an international environment |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Modeler |
| Master?s Degree in a modeling-related field with a minimum of 5 years of relevant experience, or Ph.D. with a minimum of 2 years of relevant experience, or equivalent degree/expertise. Detailed understanding of molecular & cellular biology, pharmacology, toxicology, physiology and pathophysiology, and/or pharmaceutical R&D process is desirable.
1. Experience in applying either biology, pharmacology or statistics modeling to drug R&D, and exposure to two applied areas out of three at least via collaboration on projects.
2. Good level of knowledge in one or several of the following modeling areas, and knowledge in others: learning algorithms, molecular pathways, biology, tissue effects, physiology and pathophysiology, PK/PD, statistics.
3. Basic-to-good knowledge of the drug R&D process, including clinical development; background medical knowledge and PK/PD knowledge.
4. In-depth knowledge of relevant software packages.
5. Good data exploration skills. Ability to understand heterogeneous data and communicate effectively with people from diverse scientific backgrounds in a multi-disciplinary organization.
6. Exceptional written and verbal communication skills including the ability to interact effectively with a multi-disciplinary team.
7. Good business ethics.
8. Innovative attitude; creative approach to model implementation; welcomes problems as challenges; able to approach problems from multiple angles.
9. Well-developed organizational skills; good project management skills. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Mgr/Assoc Director Product Training |
| ? Bachelor's Degree required
? A minimum of three years of pharmaceutical sales experience required
? 2+ years pharmaceutical training experience strongly preferred
? Oncology experience preferred |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Medical Scientific Expert MD(Thrombosis) |
| Strong medical science components to clinical trials/program resulting in high quality analysis of data which enables strategic decisions within the clinical program.
Novartis seen as a credible, ethical and preferred partner by key investigators in the assigned TA.
Education:
? MD with unique knowledge for successful clinical program development and execution, with ? 3 years of clinical research experience required.
Or
? MD with specialty with board certification or equivalent required.
Languages:
Fluent English (oral and written)
Experience:
? Advanced medical/scientific writing and communication skills.
? Proven ability to interpret, discuss and represent efficacy and safety data relating to the assigned area.
? Proven ability to work both independently or in a cross functional team setting, including a matrix environment.
? Demonstrated ability to establish effective working relationship with key investigators in assigned TA.
? Medical and/or scientific expertise within a disease area preferred. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Medical Scientific Expert MD(Thrombosis) |
| MD with unique knowledge for successful clinical program development and execution, with ? 3 years of clinical research experience required.
Or
? MD with specialty with board certification or equivalent required.
Languages:
Fluent English (oral and written)
Experience:
? Advanced medical/scientific writing and communication skills.
? Proven ability to interpret, discuss and represent efficacy and safety data relating to the assigned area.
? Proven ability to work both independently or in a cross functional team setting, including a matrix environment.
? Demonstrated ability to establish effective working relationship with key investigators in assigned TA.
? Medical and/or scientific expertise within a disease area preferred. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Medical Scientific Expert MD(Metabolism) |
| ? MD with unique knowledge for successful clinical program development and execution, with ? 3 years of clinical research experience required.
Or
? MD with specialty with board certification or equivalent required.
Languages:
Fluent English (oral and written)
Experience:
? Advanced medical/scientific writing and communication skills.
? Proven ability to interpret, discuss and represent efficacy and safety data relating to the assigned area.
? Proven ability to work both independently or in a cross functional team setting, including a matrix environment.
? Demonstrated ability to establish effective working relationship with key investigators in assigned TA.
? Medical and/or scientific expertise within a disease area preferred. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Medical Dir/Executive Medical Director US Medical (Respiratory) |
| An MD, Ph.D., or PharmD (MD is preferred) with a minimum of 2-3 years of Pharmaceutical or equivalent experience, some experience working in US Medcial Affairs, Clinical Research experience related to Respiratory (Allergy Research is ok but less desirable), and in leading other Medical Directors in a Pharmaceutical or equivalent environment is required.
-Ability to orchestrate and synthesize situational analyses (i.e. evidence gap analysis, customer insights, trends in therapy, etc.) across a disease area portfolio of brands to aid in the development of the disease area strategy.
-Integration of portfolio customer & stakeholder strategies with portfolio medical strategies and business drivers.
-Ability to lead in a matrixed environment and influence internal partners to achieve desired business outcomes.
-Ability to communicate effectively, manage issues, resolve conflicts, and mitigate risks.
-Prior strategic leadership experience in pharma or biotech industry.
- Prior line management experience required (3-5 years is preferred).
- Proven proficiency in stakeholder management.
-Proven leadership in clinical strategy development, trial methods, and operations.
-Experienced in presenting scientific data both verbal and written.
-Team building skills
-Understanding of the US market and the stakeholders influencing decisions.
-Advanced business and market knowledge required. Understanding of international regulations applicable to clinical development.
-Basic understanding of biostatistics p values regression correlation Statistical analysis.
-Ability to travel up to 20-25% (some Global) |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Med Scient Expert nonMD |
| MD or PhD with unique knowledge for successful clinical
program development and execution, with 3-5 years of
clinical research experience required.
- Fluent English (oral and written)
- Advanced medical/scientific writing and communication
skills
? Proven ability to interpret, discuss and represent
efficacy
and safety data relating to the assigned area.
? Proven ability to work both independently or in a cross
functional team setting, including a matrix environment.
? Demonstrated ability to establish strong scientific
partnership with key investigators in assigned TA.
? Medical and/or scientific expertise within a disease area
required; Respiratory expertise preferred |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Sr IT Project Manager/ Solutions Delivery |
| Core Project /Practice Management key to success in NIBR IT
? Understands and effectively uses different Project Management approaches
? Understands Adaptive/ Agile Project Management concepts and has used them them in project delivery
? Has strong communication and collaboration skills, successfully resolves conflict
? Has strong leadership skills and demonstrated ability to motivate a global, intra-discipline project team
? Demonstrated ability to work in a weak matrix organization
? Uses collaboration style decision making
? Effectively uses Project Management tools to facilitate decision making and enhance communication
? Has a proactive and practical approach to project delivery
? Demonstrated ability to successfully work with vendors
Technical and domain expertise
? Fully understand systems development lifecycle including configuration and customization of commercial applications (COTS) and their integration into an existing IT environment as well as in house and outsourced software development
? Has working knowledge of one or several phases of systems development lifecycle (educational or experience background in IT solution delivery)
? Understands high level concepts of Systems Architecture in a Research IT/ Pharmaceutical IT setting, including hardware and software systems (understanding of lab automation is a plus)
? Experience implementing IT solutions supporting scientific processes and decision making in Pharmaceutical or Biotech environment |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Biostatistician |
| Typically requires a Master's Degree in Statistics with at least 3 years of related experience. Typical entry level with Ph.D. in Statistics. To be considered for this level, demonstrated proficiency in the following skills and responsibilities are required: With supervision, apply advanced statistical/programming and/or PK/PD modeling in the preparation of CSRs, manuscripts, ISSs, and ISEs that meet world-wide health authority and medical community standards, and participate in protocol preparation. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Biostatistician |
| Education (minimum/desirable): At least Masters Degree in Statistics (or equivalent degree) with 7 years of experience or PhD with 4 years of experience.
Languages: Fluent English (oral and written).
Experience/Professional requirements:
1. Experience gained in the main tasks of program statistician (about 2-4 years).
2. Proven knowledge and expertise in statistics and its applications to clinical trials in at least one TA. Solid experience in drug development process and HA guidelines
3. Background medical knowledge, preferably in relation to the specific therapeutic area.
4..Good knowledge of statistical software packages.
5. Very good project management skills.
6. Very good communication and presentation skills.
7. Ability to give effective guidance to Trial Statisticians and Program Programmers.
8. Good team player. Good business ethics.
9. Good leadership skills. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| SPM/AD, Market Access & Pricing/Distribution Lead: ILARIS Brand Team |
| This person should have strong marketing experience and proven success in the areas of
pricing & reimbursement, managed care, distribution, hub development/management. Specific experience in the development of innovative payer models and distribution a must. Biologic market or other highly specialized drugs is a strong plus. Business and/or biological sciences education with concentration on marketing is preferred (MBA a plus). Sales and sales leadership experience are also highly preferred. Solid strategic thinking skills and analytical skills are essential. Strong senior management communication skills and sales force communication skills are essential.
The applicant must possess a high level of analytical and conceptual ability in order to provide strategic focus to the brand, and demonstrate a proven track record of strong execution and results. The ideal candidate will be proficient at uncovering customer based insights and leveraging this knowledge to drive brand strategy and program development. Additional requirements include the ability to lead and manage teams and multiple vendors. 20% travel is required. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Specialist III, Accounts Payab |
| Responsible for all aspects of processing vendor invoices, check requests and employee expense reports in accordance with company policy by verifying and completing accounts payable transactions and addressing related issues utilizing professional judgment.
SAP experience strongly desired and manufacturing experience preferred.
5-7 years of related experience
Associates Degree or related experience preferred. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Specialist II, Medicaid |
| Education:
BS or BA Degree preferred. High School Diploma is a minimum requirement for this position. College level credits in Finance, Accounting or Computer related studies will benefit the candidate.
Skills:
Candidate must possess accuracy and speed in data entry. It is essential to be detailed oriented and to have excellent communication skills both written as well as oral. Computer savvy with strong skills in EXCEL, word and adapt to the growing use of the internet for business purposes. SAP knowledge a plus. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Small Molecule NMR Scientist (B.S./ M.S.) |
| M.S. or equivalent with 0-5 years or more relevant experience in small molecular NMR with demonstrated success in modern NMR methodologies. Demonstrated skills in data collection and process, spectral interpretation, data management and instrument maintenance are essential. A background in organic chemistry and a keen interest to champion NMR based collaborative research projects with medicinal chemists are required. Proficiency in UNIX/LINUX and expertise in hyphenated NMR technologies are desirable. Excellent communication skills and the ability to multitask in a fast-paced environment are essential. A self-motivated individual as well as a strong team player is required. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Small Molecule Mass Spectrometry Lab Head |
| A Ph.D. scientist with 5+ years of relevant experience or an MS scientist with 10+ years of experience in small molecules MS, structure determination and open access LCMS. In-depth knowledge of mass spectrometry and related techniques and how these can be applied for the analysis of small organic molecules. Expertise in liquid and gas chromatography is expected. Expertise in automation is a plus. Excellent communication skills and the ability to multitask in a fast-paced environment are essential. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| siRNA Chemistry Associate Scientist (BS/MS) |
| ? BS or MS degree in chemistry
? 5+ years of experience in medicinal or
synthetic chemistry
? Is a creative, flexible, open minded, and
curiosity-driven scientist
? Has the ability to work effectively both
independently and with a multidisciplinary
team of medicinal chemists, biologists,
pharmacologists, engineers, and external
collaborators
? Flexibility to work in a fast-paced,
dynamic environment
? Has excellent oral / written
communication and presentation skills |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior Statistician Shanghai Chin |
| ?At least Master?s Degree in statistics or a closely related field.
?At least 5 years of experience in drug development (maybe acquired at a CRO) or a related area (2 years for Ph.D.).
?Proven knowledge of drug development and Health Authority guidelines.
?Good command of English, written and spoken.
?Ability to coordinate and oversee a team effort and to give effective guidance to programmers and to less experienced statisticians.
?Work or college experience in another country or demonstrated ability working together in a multicultural organization would be ideal.
?Advanced knowledge of statistical software, in particular SAS. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Senior Software Engineer (BS/MS) |
| The successful candidate will have a Master?s degree in computer science or equivalent experience. Along with a proven track record of building multi-tier, database-backed web applications the candidate should possess:
?Excellent interpersonal and communication skills
?Expert object-oriented programming and Java skills
?Experience with rapid development frameworks such as JBoss Seam
?Experience with Oracle, SQL, PL/SQL, and database design
?Expertise with web application servers
?Experience with Perl, C++, or languages in addition to Java
?Knowledge of Use Case design and UML
?Knowledge of service oriented architectures
?Experience handling ?omix data, especially MS based proteomics data
?At least six years of industry experience preferred |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior Scientist-Analytical |
| Education:
Minimum: BS/MS or equivalent experience.
Desirable: Advanced degree in a scientific or relevant discipline (Ph.D. or equivalent).
Languages: Fluent English (oral and written)
Experience/Professional Requirement:
1. Minimum of 3 successful years of experience as scientist (promotional pathway) or Ph.D. (0 years experience) or equivalent.
2. Awareness/proven experience for safe handling of chemicals, potentially dangerous materials and equipment.
3. Broad scientific or technical knowledge in a specific area (e.g. synthetic, analytical or galenical).
4. Adequate understanding of development processes.
5. Advanced knowledge in scientific/technical areas of collaboration.
6. Advanced knowledge of laboratory and/or technical tools.
7. Good knowledge of software and computer tools.
8. Good presentation skills and scientific/technical writing skills. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior Scientist-Analytical |
| Education:
Minimum: BS/MS or equivalent experience.
Desirable: Advanced degree in a scientific or relevant discipline (Ph.D. or equivalent).
Languages: Fluent English (oral and written)
Experience/Professional Requirement:
1. Minimum of 3 successful years of experience as scientist (promotional pathway) or Ph.D. (0 years experience) or equivalent.
2. Awareness/proven experience for safe handling of chemicals, potentially dangerous materials and equipment.
3. Broad scientific or technical knowledge in a specific area (e.g. synthetic, analytical or galenical).
4. Adequate understanding of development processes.
5. Advanced knowledge in scientific/technical areas of collaboration.
6. Advanced knowledge of laboratory and/or technical tools.
7. Good knowledge of software and computer tools.
8. Good presentation skills and scientific/technical writing skills. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Senior Scientist - Molecular Diagnostics |
| The candidate must have a Ph.D. degree in life sciences disciplines (such as Molecular or Cell Biology, Genetics or Biochemistry) with at least 3 years of postdoctoral and at least 5 years diagnostics industry experience.
* Hands-on experience on molecular biology techniques such as nucleic acid sample preparation, PCR, DNA sequencing (including next-generation), real time PCR and mutation detection.
* Familiarity with GLP and GMP environment, documentation and quality system is highly desirable.
*General knowledge with basic statistics analysis tools and understanding DOE and six sigma are also plus.
* Good communication and time management skills. In order to be successful in this position, the candidate should be a good team player in multidisciplinary environment, capable of multi-tasking, able to be fully committed to development timelines, and highly flexible in a dynamic changing environment including format and contents. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Senior Principal Scientist |
| As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
At least 7 years experience in Chemical Engineering, Polymer Science, Chemistry or a related technical field. Experience in surface chemistry, controlled release, and polymer chemistry is desired. Experience in a regulated (GxP) environment is preferred. The ideal candidate will also have experience in the scale-up and transfer to manufacturing of chemical processes, pharmaceuticals, or medical devices
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Senior PhD Scientist: Protein Purification and Expression |
| The Lab Leader of protein expression and purification group will possess the following qualifications:
?PhD with a minimum of five years of research in protein expression, purification, biochemistry or closely related discipline.
?General knowledge of state-of-the art technologies, platforms and approaches which enable practical yet innovative ways to support drug discovery programs.
?Thorough understanding of protein chemistry, biochemistry, bacterial, yeast and mammalian expression systems for tool generation to ensure the success of target-driven drug discovery.
?Strong command of academic or commercial research efforts and of scientific literature, and knowledge of key opinion leaders in the area.
The Leader of protein group will be a decisive and results-oriented individual who is flexible, team-oriented, creative and able to excel in a multi-project, fast-track environment. He or she will be a strategic thinker who interacts and collaborates with project teams, peers and management in identifying and achieving discovery goals from both scientific and strategic perspectives. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Senior Marketing Director |
| Minimum Education Requirements:
Degree in Business Admin. Marketing ? MBA desired
Minimum Experience Requirements:
8-10 Yrs. Experience in Marketing in the Life Science, FMCG?s industries
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior Investigator, Clinical PK/PD |
| Ph.D./Pharm.D. level scientist with 3 years of relevant experience, or Masters Level with at least 5 years relevant experience.
At least 3 years experience in drug development or a relevant environment (e.g. Clinical Pharmacology or Drug Metabolism and Pharmacokinetics).
Proven knowledge of PK and PK/PD evaluation techniques.
Experience of working in project teams (preferably global) and sound awareness of recent developments in drug development sciences essential.
Knowledge of regulatory requirements and experience in dealing with regulatory authorities. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior Investigator, Clinical PK/PD |
| Minimum Requirements:
Ph.D./Pharm.D. level scientist with 3 years of relevant experience, or Masters Level with at least 5 years relevant experience.
At least 3 years experience in drug development or a relevant environment (e.g. Clinical Pharmacology or Drug Metabolism and Pharmacokinetics).
Proven knowledge of PK and PK/PD evaluation techniques.
Experience of working in project teams (preferably global) and sound awareness of recent developments in drug development sciences essential.
Knowledge of regulatory requirements and experience in dealing with regulatory authorities. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior Data Manager |
| Education: Bachelors degree in life sciences, computer science, pharmacy, nursing or equivalent relevant degrees.
Languages: Fluent English (oral and written)
Experience/ Professional Requirements:
1) Ideally 5 or more years experience in drug development with at least 4 years in Data Management activities.
2) Project team leadership experience required.
3) Good technical and problem solving skills.
4) Thorough understanding of clinical trial methodology GCP and medical technology.
5) Ability to work independently, under pressure demonstrating initiative and flexibility.
6) Attention to detail and quality focused.
7) Good organization planning and project management skills.
8) Good interpersonal and communication skills and ability to operate effectively in an international environment.
9) Good negotiation skills.
10) Thorough understanding of physiology, pharmacology, clinical study objectives and the drug development process.
11) Ability to mentor, coach within Data Management and cross functionally and train internal and external partners. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Senior Business Analyst, Bioinformatics |
| Qualifications:
? Idea candidate should have an advanced degree in biology and/or B.S in Computer Science
? At least 3-5 years experience in a scientific or biotech environment
? Strong communications and interpersonal skills
? Proven capabilities interacting with scientists and being customer service oriented
? Ability to work independently and/or as part of a team
? Extensive knowledge in the biology, working experience related to the drug metabolism and pharmacokinetics research process will be strong plus
? Good understanding and practical experience in data management and data analysis tools to support research process
? Solid understanding of relational databases and familiarity with Oracle and/or SQL server
? Strong software engineer knowledge and extensive practical experience |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior Brand Manager-Prevacid |
| ? MBA
? 5+ years of consumer packaged goods marketing experience. Prior experience in healthcare industry and knowledge of regulatory issues impacting the industry preferred.
? Broad knowledge of healthcare and OTC industry, markets, and competitive products, new business development experience. Broad knowledge of market research data sources and applications. OTC product launches or switch experience.
? Creative problem solving skills
? Excellent analytical skills
? Strong leadership skills particularly of cross-functional teams
? Strategic thinking potential and proactive self-starter
? Significant knowledge of sales and marketing techniques, market research data sources and applications, is required.
? Personal computer efficiency required (Word, Excel, PowerPoint, Lotus Notes preferred).
? Well-developed oral, written and analytical skills.
? Requires significant amount of innovation and creativity to champion profitable products to market quickly. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior Brand Manager |
| - Creative problem solving skills
- Excellent analytical skills - - Stong leadership skills particularly of cross-functional teams
- Strategic thinking potential and proactive self-starter.
- Significant knowledge of sales and marketing techniques, market research data sources and applications, is required.
- High efficiency with Word, Excel, PowerPoint, Lotus notes prefer.
- MBA (Marketing concentration) preferred.
- Must have 5+ years of consumer packaged goods marketing experience.
- Well-developed communication skills
Preferred:
- Knowledge of regulatory issues impacting the industry
- Broad knowledge of healthcare and OTC industry, markets, and competitive products, new business development experience.
- Knowledge of market research data sources and applications. OTC product launches or switch experience. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior / p-CRF Developer |
| BA/BS in life science, computer science, pharmacy, nursing or equivalent.
Fluent English (oral and written).
1. 2-5 years working experience in software based paper forms design
2. University degree in Life Sciences, Mathematics, Computer Science, Medical Informatics or equiva-lent degree
3. Solid knowledge of medical terminology.
4. Exposure to knowledge of Clinical Research prac-tices and procedures, stages of clinical trials, drug development process, requirements and guidelines for data collection.
5. Solid knowledge of the software used with pCRF design in EDM, specifically the electronic publishing system for pCRF production.
6. Solid communication skills in order to be able to work with a wide variety of customers both face-to-face and via phone or e-mail. Requirement for excel-lent ENGLISH.
7. Exposure to ICH and Health Authority guidelines and regulations as they pertain to clinical database management and computer systems |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Scientist, Translational Safety Biomarker Lab |
| Educational requirements:
BS/MS degree in Biochemistry or Molecular
and/or Cell Biology, Biomedical engineering,
or related fields.
Experience:
5 or more years of practical experience in
assay, reagent, and technology development
in the life sciences industry. The successful
candidate will have experience in molecular
and/or chemical approaches to affinity-
reagent generation. It would be beneficial to
have experience working with biomarker
development, exposure to in vivo studies
both preclinical and/or clinical. The
preferred candidate will have expertise in
data summarization and analysis, oral and
written communication skills. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Scientist, Metabolic Pathways |
| M.S. in Chemistry or Biochemistry or related field with a minimum of three years or B.S. with five years of hands-on with HPLC and LC-MS/MS. Prior experience with radioisotope handling (e.g., 3H, 14C), biochemical techniques and in vivo and in vitro metabolism is required. The candidate should be capable of working independently under moderate supervision and should possess good writing and verbal communication skills. An excellent working knowledge of general laboratory techniques, HPLC and LC-MS/MS operation, and troubleshooting and method development is essential. A strong background in analytical problem solving is also required. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Scientist-Analytical |
| Education
Minimum: BS or equivalent experience.
Desirable: MS or equivalent.
Languages: Fluent English (oral and written)
Experience/Professional requirement:
1. Minimum of 3 successful years of experience as associate scientist (promotional pathway) or 3-5 year's (for BS) or 1-3 year's (for MS).
2. Awareness/proven experience for safe handling of chemicals, potentially dangerous materials and equipment.
3. Good scientific or technical knowledge in a specific area (e.g. synthetic, analytica or galenical).
4. Adequate knowledge in scientific/technical areas of collaboration.
5. Proficient with laboratory and/or technical tools.
6. Adequate knowledge of software and computer tools.
7. Basic presentation skills and scientific/technical writing skills. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Scientist II |
| Education & Experience
BS degree required 4 - 8 years of related experience 2+ years demonstrated experience with method development |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Scientist I - Molecular Toxicology |
| Minimum Requirements
Technical Skill Sets:
? Demonstrated competence in performing a variety of molecular biology techniques (e.g. nucleic acid purification, cloning, TaqMan and SYBR green qPCR, siRNA/shRNA knockdown, etc?)
? Proficiency in isolating and cultivating cells from different organs in different species
? Demonstrated competence in performing a variety of biochemical techniques (e.g., preparation of cell and tissue extracts, subcellular fractionation, enzyme assays, protein detection assays (Western blotting, ELISA, Luminex, MSD?))
? Extensive experience with preclinical animal models, including animal handling, study design and protocol implementation, IV and oral dosing, and necropsy procedures
? Good understanding of SOPs as well as their practical implementation
? Fluency in English
? Working knowledge of relevant IT systems and software
Experience:
? At least 5 years of experience in cellular/molecular biology and/or toxicology in academic and/or industrial environment
? Excellent knowledge of mammalian cell culture models (primary cultures and cell lines) and related techniques
? Excellent knowledge of molecular & biochemical analytical techniques
Personal Skill Sets:
? Interpersonal and teamwork skills
? Independent and proactive work ethic
? Outstanding oral communication and writing skills
? Computer skills for experimental organization, assay design, data collection and analysis, and report writing
Education:
Bachelor?s or Master?s degree in life sciences, preferably molecular biology, biochemistry, cell biology, or molecular toxicology |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Scientist I |
| Education & Experience
BS, MS, or PhD, Chemistry, or other scientifically related field. BS degree + 5 or MS +3 years experience as an analytical chemist or MS, Chemistry with 2+ years experience within method development. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Scientist I |
| Minimum 5 years of laboratory experience. Experience with immunofluoresence, fluorescent microscopy and image analysis is required. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Scientist I |
| Bachelor?s Degree in analytical chemistry or a related discipline plus at least 5 years (or M.S. and 3 years) of relevant experience in quantitative analytical techniques involving the automated extraction and analysis of small and/or large molecules in biological samples using LC-MS/MS. Experience in a GLP laboratory environment, proficiency with personal computer applications for word processing, spreadsheets and graphics, as well as good oral and written communication skills are desirable. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Scientific Associate: Oncology Biotherapeutics |
| Candidates should possess a BS/MS degree with 2-5 years of relevant laboratory experience. Candidates who have worked in the Pharma/ Biotech industries are particularly encouraged to apply. Knowledge of cell signaling pathways as related to oncology or other proliferative diseases is crucial. It is essential that you have an excellent working knowledge and direct experience of a breadth of cellular and molecular biological methods (especially RNAi, RT-qPCR, cloning, cell culture, transient/ stable cell line generation, immuno-detection, ELISAs and phenotypic characterization). You should be a scientifically motivated self starter, capable of independently conceiving, conducting and critically analyzing your own innovative experiments. Strong presentation skills, communication and the ability to work in a fast-paced team-oriented environment will also be vital. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Scientific Associate II |
| ? B.S. or M.S. in Analytical Chemistry, Biochemistry or related life science field with a strong background in protein analytics.
? Minimum of 3 years of relevant academic or industrial laboratory experience; hands-on experience with HPLC and CE techniques is required. Experience with mass spectrometry would be a plus.
? Must have excellent written and oral communication skills and demonstrate ability to work both independently and as part of a team.
? Successful candidate should be self-motivated and capable of multi-tasking with strong problem solving skills. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sales Training Business Partner |
| ? Bachelor?s degree
? MBA preferred
Experience:
? 6-8 years professional experience (sales, marketing, operations, management)
? > 2 years of experience in training organization
? Analytic, strategic and creative thinking
? Innovative mindset
? Knowledge of sales training and development processes
? Strategic and business acumen
? Strong prioritization, negotiation and influencing skills
? Knowledge of adult learning principles & concepts
? Strong oral, written and platform skills
? 3 to 5 years of Pharmaceutical industry experience preferred
? Understanding of Novartis BU structure and markets |
| Novartis Oncology |
na |
AR |
9/4/2010
|
| Sales Analyst-Walmart |
| ? Bachelor?s Degree
? Demonstrate advanced knowledge of Excel, Word, powerpoint, and Access
? Flexible with traditional work hours: willing to work several hours on Sunday evening from home or early AM hours on Monday to meet deadlines
? Exceptional Communication and Interpersonal skills
? Able to work in a fast-paced environment with demonstrated ability to juggle multiple competing tasks and demands.
? Preferred experience within Consumer Products Goods Company |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Safety Toxicologist |
| ? BS or MSc degree and major in physiology, pharmacology, biomedical engineering or related field.
? Prefer 5 ? 10 years experience in cardiovascular physiology and/or pharmacology research.
? Prefer minimum of 2 years experiences in cardiovascular safety pharmacology research.
? Experience in setting up, conducting and reporting of telemetry studies in dog and monkey.
? Familiar with EMKA jacket system or other external jacket telemetry system and have experience in EMKA ECGAuto computer software (or similar computer software) to analyze cardiovascular telemetry data.
? Experience in using Excel and SAS macro to analyze and report cardiovascular parameters in telemetry.
? Experience in ECG analyses including ECG interval measurements and waveform abnormalities screening in dog and monkey. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Respiratory Specialist - Toms River, NJ PEXC1E |
| ? Bachelor?s Degree (preferably in Life Sciences, Pharmacy or Business related discipline).
? Minimum of 4+ years of Specialty sales experience selling in the Respiratory/Allergy and/or Infusion market and interacting with Allergists, Pulmonologists, and other key customers.
? Track record of success in account based selling models within Specialty Markets
? Knowledge and understanding of distribution and reimbursement models used for Specialty/Biologic products.
? Demonstrated superior business acumen and business planning skills.
? Proven ability to collaborate and work cross functionally with internal and external partners.
? Possess high achievement drive, self-motivation, and willingness to mentor others
? Effective problem solving, decision making and interpersonal skills (both internal and external).
? Exceptional customer relationship building skills.
? Strong Analytic and Computer literacy skills. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Research Scientist: Biochemistry and Affinity Proteomics (BS/MS) |
| Candidates should have a BS or MS in Biochemistry or Biological Science with 3-8 years academic and/or industry experience. They must be well-versed in all aspects of protein purification including sample preparation, chromatographic and gel-based separations, electrophoresis, and cell culture. They should have experience in the design and implementation of biochemical assays and in data analysis. The ideal candidate is an independent worker, a self-starter, good at trouble shooting and thriving in a multidisciplinary environment. Excellent communication skills are required and a premium is placed on candidates with a track record of creativity and innovation.
Additional Experience:
Experience with activity-based probes, photoaffinity crosslinkers, sub-cellular fractionation, basic molecular biology techniques, and sample preparation for mass spectrometry is a plus. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Research Scientist ? RNAi Therapeutics (BS/MS) |
| This position requires a Bachelor?s or Master?s degree in Biology, Cell/Molecular Biology, Biochemistry, Genetics, or related field with 5-10 years of academic or industrial research experience. Proven track record of innovative project contributions including peer-reviewed publications is desired. The successful candidate will have extensive experience with basic molecular and cellular biology techniques such as mammalian cell culture, siRNA technologies, real-time PCR, molecular cloning, and compound efficacy profiling. Experience in high-throughput screening technologies and in-vivo animal models are a plus. Good organizational and analytical skills, a working knowledge of data management, word processing, and graphing software are essential. Additionally, the ideal candidate will have excellent oral/written communications skills with the ability to work both independently and in the context of a multidisciplinary team of chemists, biologists, and pharmacologists. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Research Scientist |
| Education requirements:
BS or MS in chemistry or related scientific discipline with 2+ years experience in a laboratory setting
or
Entry-level PhD in Chemistry or related scientific discipline.
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Research Investigator, Preclinical Imaging, Investigative Toxicology |
| ? Ph.D. degree in Biochemistry, Physiology, Pharmacology, Toxicology, Biophysics, Biomedical Engineering or related field in the biomedical sciences
? At least 2 years of prior experience in pharmaceutical drug development and/or toxicological sciences required.
? Experience with hands-on in vivo small animal imaging, preferably with multiple imaging modalities. A strong expertise in small animal (rat, mouse) Ultrasound imaging for various applications including contrast enhanced ultrasonography is preferred.
? Expertise and knowledge in vascular toxcology and in vitro vascular ring assay would be a plus.
? Experience of managing highly skilled technical staff, laboratory equipment, consumables and safety is desirable.
? Fluency in English (written and spoken) is a must
? Flexibility and ability to work in a team, comfortable with multitasking, excellent interpersonal skills to communicate and collaborate within a multi-disciplinary environment, willingness to take on additional responsibilities are expected
? Excellent project management skills
Technical Skill Requirements:
? Experience with pre-clinical applications of MR imaging and spectroscopy, X-ray microCT, ultrasound and/or optical imaging
? Imaging data processing and analysis |
| Novartis Oncology |
na |
CO |
9/4/2010
|
| Research Chemist III |
| Educational/Professional Requirements:
?BS/BA in Chemistry or life sciences
?4 years of professional related experience
?Relevant experience in a GMP laboratory and R&D lab/ production environment.
?Infrequently lifting 5kg to waist height,
?Approx 10% on floor time (Walking/Standing)
?Limited Travel (1-5 times/yr.)
Skills & Competencies:
?Has thorough understanding of technical concepts required for raw material testing, method development, evaluation and optimization.
?Requires working knowledge of Microsoft office applications. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Research Associate, Molecular Imaging, PET/SPECT/CT |
| The ideal candidate will have a BS/MS in Biology, Biochemistry, Animal Sciences, Bioengineering, Biophysics or related field, and 3+ years of hands-on experience with PET/SPECT/CT imaging is a requirement, ideally in a drug discovery environment. Good organizational, interpersonal skills, and excellent communication and presentation skills are desirable.
Skills required: Technical proficiency in all aspects related to PET and extensive hands-on experience with small animal handling (including tail vein injection, catheter placement, perfusion, microdissection), and in vivo pharmacology. Strong computer/computational skills in data analysis. Creativity and the ability to work independently. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Research Associate BS/MS - Biochemistry/Enzymology |
| The successful candidate should have a Bachelors/Masters in biochemistry or a related area of biological sciences with at least 2 years of laboratory experience in industry or academic setting. Experience in biochemical and biophysical assay development, enzyme kinetics is desirable. Knowledge and hands-on experience in applying modern biophysical/analytical techniques, such as fluorescence spectroscopy, Surface Plasmon Resonance, Calorimetry and LC-MS, are a plus. Must be self-motivated and detail-oriented. Is highly organized and has ability to handle multiple tasks. Proficiency in data handling with standard computer programs is a must. The candidate should have strong communication and interpersonal skills. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Research Associate - Cell Biology and Molecular Virology |
| Qualified candidates will have a BS/BA or Master?s degree in biology or related field, with strong data management skills and extensive molecular/cell biology expertise. The candidate should have experience in experimental design, data interpretation and statistical analysis. A strong work ethic, excellent oral and written communication skills, and ability to function in an interdisciplinary team setting are required. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Regulatory Associate |
| Minimum Education Required:
HS or equivalent. BS in scientific discipline preferred.
Minimum Experience Required:
3 years employment in the areas of product registration, compliance or quality systems.
Experience gained through employment in a medical device or drug company preferred.
Minimum Skills Required:
Familiar with global registration and compliance requirements.
Competent in basic documentation requirements.
Basic word processing skills.
Good communications skills (verbal and written).
Computer literacy with CIBA VISION standard software platforms.
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules. |
| Novartis Oncology |
na |
SC |
9/4/2010
|
| Regl Scientific Mgr/Dir--Primary Care (North Carolina/South Carolina) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Therapeutic Areas and/or in a Field-based position is a definite asset. Salary flexible.
Ability to travel approximately 60%. |
| Novartis Oncology |
na |
CA |
9/4/2010
|
| Regl Scientific Mgr/Dir Southwest OU--Respiratory (Northern CA) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Respiratory Therapeutic Areas and/or in a Field-based position is a definite asset. Salary flexible. |
| Novartis Oncology |
na |
MO |
9/4/2010
|
| Regl Scientific Mgr/Dir Southwest OU--Respiratory (AR, KS, and MO) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Respiratory Therapeutic Area and/or in a Field-based position is a definite asset. Salary flexible. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Regl Scientific Mgr/Dir Southeast OU--IDTI (AL, FL, GA) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Infectious Diseases, Transplantation and Immunology Therapeutic Areas and/or in a Field-based position is a definite asset. Salary flexible. |
| Novartis Oncology |
na |
NE |
9/4/2010
|
| Regl Scientific Mgr/Dir NW OU--Primary Care (IA and NE) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Cardiovascular, Endocrinology, and Rheumatology Therapeutic Areas and/or in a Field-based position is a definite asset. Salary flexible. |
| Novartis Oncology |
na |
WA |
9/4/2010
|
| Regl Scientific Mgr/Dir NW OU--Primary Care (AK and WA) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Cardiovascular, Endocrinology, and Rheumatology Therapeutic Areas and/or in a Field-based position is a definite asset. Salary flexible. |
| Novartis Oncology |
na |
UT |
9/4/2010
|
| Regl Scientific Mgr/Dir NW OU--Multiple Sclerosis (CO, IA, NE, UT) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Multiple Sclerosis or Related Therapeutic Areas and/or in a Field-based position is a definite asset. Salary flexible. |
| Novartis Oncology |
na |
PA |
9/4/2010
|
| Regl Scientific Mgr/Dir NE OU--Multiple Sclerosis (Phila/Southcent PA) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Mutiple Sclerosis or Related Therapeutic Areas and/or in a Field-based position is a definite asset. Salary flexible. |
| Novartis Oncology |
na |
NY |
9/4/2010
|
| Regl Scientific Mgr/Dir NE OU--Multiple Sclerosis (New York City) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Multiple Sclerosis or related Therapeutic Areas and/or in a Field-based position is a definite asset. Salary flexible. |
| Novartis Oncology |
na |
AZ |
9/4/2010
|
| Regl Scientific Mgr/AD, Hematology MSL, Southwest US |
| Position will be filled at level commensurate with experience. Advanced scientific degree (MD, PhD, or PharmD highly preferred) or oncology nurse with advanced degree required. Minimum of 5 years Oncology experience with a strong current working knowledge of Oncology required. Teaching experience preferred. Previous pharmaceutical industry experience preferred. Thought leader development experience is a plus. Knowledge of treatment guidelines, clinical research processes, FDA regulations and OIG guidelines is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important external customers, including medical thought leaders, academic institutions, large group practices, medical directors and pharmacy directors is required. Must be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society (ies) is a plus. Must be a strong team player who can effectively interface cross-functionally with Novartis clinical and commercial personnel. Working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel) and associated hardware is required. The position is associated with approximately 65% travel. |
| Novartis Oncology |
na |
MS |
9/4/2010
|
| Regional Sales Director - Jackson, MS or Birmingham, AL. |
| Minimum Education Required:
BS/BA in related field. MBA preferred.
Minimum Experience Required:
10+ years experience in outside sales in business to business selling models using consultative selling approaches including a minimum of three (3) years of Sales Management experience.
Demonstrated experience developing and promoting Sales employees.
Proven market analytical sales resulting in performances that exceed company expectations.
Preferred Experience Level:
10+ years business-to-business selling in combination with medical sales experience.
5+ years Front Lines Sales Management experience with a history of exceeding District/Region Sales and Market Share.
People management accountability required. |
| Novartis Oncology |
na |
PR |
9/4/2010
|
| Regional Medical Associate Director/Director (Puerto Rico) |
| The candidate must be locally based in Puerto Rico.
Position will be filled at level commensurate with experience:
Advanced scientific degree (M.D., Ph.D., or PharmD; M.D. is preferred). A minimum of 3 years of Postdoctoral experience in pharmaceutical industry (preferred) or other healthcare/managed markets environment.
Excellent interpersonal and oral and written communication skills in both English and Spanish are required.
Field based medical and/or managed care with teaching experience preferred.
Thorough knowledge of clinical medicine, managed markets, pharmacoeconomics, disease management, medical research and health policy in Puerto Rico are required.
Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations and ethical guidelines applied to the pharmaceutical industry preferred. Excellent presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, pharmacy directors and government officials is required. Must be science-oriented and be able to prioritize work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer?s unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, Powerpoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Operating Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RMAD/D position is associated with approximately 60% travel. Salary flexible. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Regenerative Medicine Research Associate (BS/MS) |
| Candidates should have a BS or MS in an appropriate discipline as well as 3 or more years relevant experience. The successful candidate should have demonstrated experience with stem cell isolation, culture and characterization, complex cell-based assays and imaging-based screens. Experience in studying the development or regeneration of specific organs such as pancreas, kidney, eye, lung, intestine or skin would be of high interest.
Excellent communication skills and ability to work in a team is required. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| R&D Quality Engineer |
| Education Requirements:
Bachelor of Science degree in Reliability, Quality, Mechanical, Electrical Engineering, Math, Physics or equivalent.
Experience Requirements:
Minimum 5 to 10 years experience in Reliability engineering and testing. Medical Device experience preferred.
Ability to interpret, analyze, and present technical information using practical judgement.
Capable of functioning effectively in a team environment.
Proficient in Excel pivot tables and charting.
Excellent written and oral communication skills.
Demonstrated problem solving skills.
Ability to organize and manage concurrent activities.
Knowledge of advanced data gathering and analysis techniques, including statistical analysis.
Knowledge of standard quality and reliability tools such as FMEA (Failure Modes Effect Analysis), Root Cause Analysis, DOE and Statistics.
Proven ability to communicate effectively and manage relationships at all levels of the organization as well as cross-functionally to achieve reliability goal.
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| R&D Quality Engineer |
| Education Requirements:
Bachelor of Science degree in Reliability, Quality, Mechanical, Electrical Engineering, Math, Physics or equivalent.
Experience Requirements:
Minimum 5 to 10 years experience in Reliability engineering and testing. Medical Device experience preferred.
Ability to interpret, analyze, and present technical information using practical judgement.
Capable of functioning effectively in a team environment.
Proficient in Excel pivot tables and charting.
Excellent written and oral communication skills.
Demonstrated problem solving skills.
Ability to organize and manage concurrent activities.
Knowledge of advanced data gathering and analysis techniques, including statistical analysis.
Knowledge of standard quality and reliability tools such as FMEA (Failure Modes Effect Analysis), Root Cause Analysis, DOE and Statistics.
Proven ability to communicate effectively and manage relationships at all levels of the organization as well as cross-functionally to achieve reliability goal.
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Quantitative Mass Spectrometry Research Associate (BS/MS) |
| BS/MS in biology or chemistry with a minimum of two years experience with compound quantitation using triple quadrupole mass spectrometers; No experience in proteomics mass spectrometry required; In-depth knowledge and hands-on experience with LC/MS of compounds or peptides; Direct experience with operation, maintenance, and troubleshooting of triple quadrupole mass spectrometers; Extensive experience with compound or peptide quantitation using SRM/MRM and internal standards. |
| Novartis Oncology |
na |
CA |
9/4/2010
|
| Quality Control Scientist |
| BS in Micro Biological Science or equivalent discipline. Minimum of 5-7 years of related experience or equivalent. Thorough knowledge of chemical, microbiological, and EM test methods. Proficient in performing benchtop microbiology techniques. Thorough knowledge of GMPs/GLPs. Strong communication skills. Requires handling of chemicals such as acids, alkalis, solvents and powdered media; Work with biohazardous agents such as E. coli or S. cerevisiae; Requires bending and reaching throughout the work shift in support of wide range of activities such as valve adjustment, fastening of hoses and/or connections and conducting cleaning activities; Requires walking / standing for extended periods (up to 6 hours) throughout the work shift; May require dexterity for fine motor tasks such as pipetting and sterile manipulations in biosafety cabinets (periods up to 2 hours); May need to adapt to changing work shifts, both swing and/or graveyard on very short notice; May use a computer for greater than 4 hours a day. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Quality Control Analytical Lab Supervisor |
| Minimum Education and Experience Requirements:
Requires a Bachelors degree in Chemistry or related science from and accredited college or university with a minimum of 7 years of experience overall with 5 years supervisory experience in a regulated laboratory, preferably in a pharmaceutical laboratory environment.
Requires solid knowledge of quality control systems, including FDA compliance standards, regulations, and guidelines.
Requires excellent oral and written communication, organizational and teamwork skills.
n equivalent combination of education, experience and training may substitute.
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| PTM (Project Team Member), Strategic Marketing, GPS |
| University degree in Medicine, Biological or Pharmaceutical Sciences. An advanced degree in bioscience, and/or business is a plus (e.g., MD, Pharm. D., PhD., MBA)
Strong science and business background
? Excellent understanding of Oncology market
? Extensive contact with Oncology/Hematology Medical experts
? Proven ability to operate and influence cross-functionally and cross culturally
? Proven leadership ability
? Strong analytical and strategic thinking skills
? Oncology product development experience
? Significant experience in launching new products |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Proteomics and Mass Spectrometry Scientist (BS/MS) |
| BS/MS in biology or chemistry with >5 years experience in a mass spectrometry laboratory. In-depth knowledge and hands-on experience with LC/MSMS and ESI of proteins and peptides. Excellent communication skills and the ability to multitask in a fast-paced environment are essential.
Experience in cell biology or cell culture is a plus. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Protein NMR/Biophysics Research Associate (BS/MS) |
| B.S/M.S. or equivalent in biochemistry or a related discipline with at least 2 years of research laboratory experience. Experience in protein handling/characterization and laboratory automation is required. Attention to detail, an ability to work independently, and multitasking skills are expected. Experience with NMR spectroscopy and/or biophysical characterization of proteins and computational skills would be a decided asset. The candidate must possess good oral and written communication skills and should be able to function well in a matrix managed environment. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Protein Biochemistry Research Associate (BS/MS) |
| B.S/M.S or equivalent in biochemistry or a related discipline with at least 2-3 years of research laboratory experience. A strong background in protein expression and purification is highly desirable. Molecular biology experience is also an important pre-requisite. Must be detail oriented and be able to handle multiple tasks efficiently. The candidate must possess good communication skills and be comfortable working in a matrix based team environment. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Protein Biochemistry Research Associate (BS/MS) |
| B.S/M.S or equivalent in biochemistry or a related discipline with at least 2-3 years of research laboratory experience. A strong background in protein expression and purification is highly desirable. PhD level scientists should not apply.
The successful candidate will be expected to be able to participate in experimental design and to independently conduct experiments. They must also be detail oriented and be able to handle multiple tasks efficiently. The candidate must possess good communication skills and be comfortable working in a matrix based team environment. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Protein Biochemistry Research Associate (BS/MS) |
| B.S/M.S or equivalent in biochemistry or a related discipline with at least 5 years of research laboratory experience. A strong background in protein expression and purification is highly desirable.
The successful candidate will be expected to be able to participate in experimental design and to independently conduct experiments. They must also be detail oriented and be able to handle multiple tasks efficiently. The candidate must possess good communication skills and be comfortable working in a matrix based team environment. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Program Section Leader (MD) Thrombosis |
| Education (minimum/desirable):
MD, required
Advanced knowledge in medical/scientific area required.
Languages:
Fluent oral and written English.
Experience/Professional requirement:
? ?8 years of involvement in drug development spanning clinical activities in Phases II/IV or comparable experience in industry.
? ?4 years of demonstrated leadership and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing), or section of clinical programs in a global/matrix environment (including remote) in pharmaceutical industry.
? ?4 years people management experience required, this may include management in a matrix environment. Global people management experience desirable.
? Strong management, interpersonal, communication, negotiation and problem solving skills.
? Considerable organization awareness (e.g., inter-relationship of departments, business priorities), including significant experience working cross-functionally and in global teams.
? Medical/scientific and operational expertise appropriate to the program. |
| Novartis Oncology |
na |
TX |
9/4/2010
|
| Professional Services Vet-Cattle |
| ? DVM or equivalent
? 5 years with Novartis Animal Health with consistently high performance ratings or 7 years or more professional experience with listed qualifications
? Advanced degree in medical specialty, practice management or business administration encouraged
? Marketing/Sales Management experience |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Product Safety Specialist |
| Minimum Experience Required:
1-2 years experience within contact lens or medical device industry within one of the following functions: manufacturing, quality affairs, customer service, or product consultation
Preferred Level:
3-5 years complaint handling, adverse event reporting or product quality risk in a medical or pharmaceutical regulated environment.
2 years experience dealing with healthcare professionals and/or consumers.
Ability to work independently in fast-paced environment with little supervision.
Detail oriented, and ability to multitask.
Computer literacy with Microsoft Office,Lotus Notes and Trackwise.
Excellent written and verbal communication skills are essential
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
NC |
9/4/2010
|
| Procurement/Sourcing Manager |
| Bachelor?s degree required at a minimum, master?s degree preferred in fields such as Supply Management, or a scientific or technical field. Strong preference for CIPS or similar professional qualification.
5-10 years of Procurement experience in a pharmaceutical manufacturing or regulated (GMP) product environment. Extensive experience in category and demand management, collaborative cost reduction and productivity programs, activity-based cost analysis, and negotiation. Technical experience with pharmaceutical chemicals and associated materials. |
| Novartis Oncology |
na |
NE |
9/4/2010
|
| Process Engineer |
| Required: BS degree in an appropriate scientific, pharmaceutical or engineering discipline and 3 to 5 years of demonstrated experience in pharmaceutical formulation, packaging engineering, and/or process development. Experience with pharmaceutical production practices, manufacturing and packaging equipment, and instrumentation and controls. Working knowledge of GxPs. Demonstrated ability to execute facility, process, computerized system, cleaning, and equipment validations.
Preferred: Packaging Engineer or Electrical Engineer with advanced degree. Prior accomplishments in pharmaceutical formulation, development for various dosage forms, or packaging engineering in relevant environments. Prior experience executing capital projects. Working knowledge of analytical testing preferred; demonstrated experience with quality engineering methodology desired.
Only on-line resumes will be accepted.
If you require accommodation under the American?s with Disabilities Act to apply for this position,
contact Suzanne Drew (402) 467-8808. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Principle Medical Scientific Expert MD (CV) |
| Education:
? MD with unique knowledge for successful clinical program development and execution, with ? 3 years of clinical research experience required. Preference for 2+ years of industry experience
Or
? MD with specialty with board certification or equivalent required.
Languages:
Fluent English (oral and written)
Experience:
? Advanced medical/scientific writing and communication skills.
? Proven ability to interpret, discuss and represent efficacy and safety data relating to the assigned area (Cardiovascular)
? Proven ability to work both independently or in a cross functional team setting, including a matrix environment.
? Demonstrated ability to establish effective working relationship with key investigators in assigned TA (CV).
? Medical and/or scientific expertise within the Cardiovascular disease area. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Principal Scientist, Preformulation |
| Education & Experience
14-19 Years with Bachelors of Science, 12-17 years with Master of Science, 9-14 years with PhD |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Principal Scientist - Salt and Polymorphism Expert |
| Education (minimum/desirable):
Minimum: BS/MS organic/analytical chemistry with 7-10 years of experience in solid state chemistry of APIs.
Desirable: Ph.D. organic/analytical chemistry or equivalent education with strong emphasis on solid state chemistry with 3-5 years of experience in pharmaceutical industry (knowledge of molecular modeling and GMPs would be a plus). Experience with form selection, polymorphism, and physicochemical characterization of APIs. Familiarity with current analytical instrumentation and techniques to characterize API forms using FBRM, XRPD, DSC, TGA, vibrational spectroscopy, UV-Vis, vapor sorption, GC, HPLC, size and solubility measurement, with an emphasis on laboratory automation. Excellent written and verbal communication skills. Good project management, time management, and decision making skills.
Languages: Fluent English (oral and written)
Experience/Professional requirement:
1. Successfully demonstrated several years (minimum of 3 years)of directly related experience as senior scientist or equivalent in pharmaceutical R&D.
2. Documented scientific/technical expertise in form selection, polymorphism, and characterization of APIs.
3. Successfully demonstrated track record of creativity and problem solving in projects.
4. Proven track record in utilization of special tools/equipment, lab automation tools and specialized facilities.
5. Profound literature search skills.
6. Strong presentation skills and scientific/technical writing skills.
7. Proven scientific leadership skills.
8. Ability to work in interdisciplinary teams.
9. Familiarity with the current analytical instrumentation and techniques to characterize crystalline and amorphous materials.
10. Familiarity with GLPs as applied to pharmaceutical industry. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Principal Scientist - Formulation |
| Education
Mminimum: Technician with continuing education (EU) or BS/MS or equivalent.
Desirable: Advanced degree in a scientific or relevant discipline (Ph.D. or equivalent).
Languages: Good knowledge of English (oral and written). Desirable knowledge of site language.
Experience/Professional requirement:
1. Successfully demonstrated several years (minimum of 3 years) of directly related experience as Senior Scientist or Ph.D. with post-doctoral/industrial experience (minimum of 1 year) or equivalent.
2. Successfully demonstrated expertise in a specific scientific/technical area.
3. Recognized achievements in the development of new lab/plant procedures.
4. Excellent knowledge of laboratory and/or technical tools.
5. Proficient in utilization of special tools/equipment, lab automation tools and specialized facilities e.g., containment/sterile labs.
6. Thorough understanding of development activities and processes in a specific function.
7. Good knowledge of software and computer tools.
8. Profound literature search skills.
9. Good presentation skills and scientific/technical writing skills.
10. Strong scientific leadership skills.
11. Strong knowledge of relevant SOP, GLP, GMP and Novartis regulations and policies.
12. Very good communication skills, advanced coaching skills.
13. May require up to 15% travel.
Experience with drug delivery technologies and application to solid dosage forms preferred. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Principal Clinical Scientist |
| Education:
O.D. degree (or equivalent)
Experience:
4 years in product development and/or research.
Skills:
Working knowledge of experimental design, clinical trial im-plementation and management, and data analysis.
Proficient in MS Word, Excel, and PowerPoint.
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Presidential Post Doctoral Fellow |
| Multiple positions exist at all sites of Novartis Institutes for BioMedical Research for individuals with the following minimum requirements: Ph.D. in biological sciences, chemistry, or computer science. Applicants who have commenced postdoctoral training may apply as well, but they should not have been in postdoctoral training for more than 3 years. Candidates must be able to work independently and also participate in team efforts. Excellent oral / written communication and presentation skills and scientific creativity are essential. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| PhD Scientist: Ophthalmology Pharmacology: Target ID/Validation |
| The ideal candidate will have a Ph.D. in Developmental Biology, Cell Biology, Immunology or Ophthalmology with 3-5 years of relevant post doctoral training and demonstrated expertise in molecular mechanisms and pathways. A solid background in ophthalmology research is preferred. Strong organizational, leadership and both oral and written communication skills, along with a track record of scientific accomplishments and a desire to work in a team focused environment are essential. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| PhD Scientist: Ophthalmology Pharmacology: Ocular Drug Delivery |
| The ideal candidate will have a Ph.D. in Pharmaceutical Sciences, Pharmacology, Ophthalmology, Physiology, Cell Biology or Immunology with 3-5 years of relevant experience after completion of post doctoral training and demonstrated expertise in drug delivery, drug disposition and pharmacokinetics. Strong organizational, leadership and both oral and written communication skills, along with a track record of scientific accomplishments and a desire to work in a team focused environment are essential. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| PhD Scientist: Oncology Biotherapeutics Lab Head |
| Candidates should possess at least 2 years post-doc experience, ideally in a world renowned signaling lab. Previous drug discovery experience is not a prerequisite for this position. Your role will be to lead from the lab, the generation of data that increases our biological understanding of emerging cancer targets and elucidates the mechanism of action of biotherapeutics at the molecular and cellular level. In addition, you will be expected to participate in global multidisciplinary project teams and ultimately lead the discovery, direction, and productivity of a small molecular/cell biology laboratory. This is an excellent opportunity for the successful candidate to grow into a project team leader.
Desired experience:
? Ph.D. in cancer genetics or cell signaling.
? Minimum 2 years of high quality post-doctoral experience in cancer genetics or cell signaling
? Independent, self motivated and innovative personality
? Excellent written and oral communication skills
? Demonstrated publication record
? Previous evidence of coaching or mentoring skills would be advantageous |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| PhD Scientist: Antibody Therapeutics |
| Molecular Biology lab head Qualifications:
? Ph.D. in molecular biology or life science
? Minimum 3 years of post-doctoral experience in life-science and/or antibody therapeutic research. Industry experience is a plus.
? Self-driven and creative personality
? Excellent written and oral communication skills
? Extensive experience in molecular biology, cell and biochemical assay development and analysis |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| PhD Scientist-In Vivo Physiology ? Muscle Disease |
| The position requires a Ph.D degree in a relevant field with a minimum 4-6 years of post-doctoral laboratory experience preferably in an industry setting. Strong skills in in vivo physiology, especially in skeletal muscle models. Also experience in establishing muscle models of disease is needed. The individual should have strong leadership skills, and strong potential to become a leader in the field of muscle research. Strong oral and written communication skills and a demonstrated ability to work in a team-oriented environment are essential. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| PhD Scientist- Oncology Biology |
| Qualifications:
? Ph.D. molecular biology or related field
? Minimum 3 years of post-doctoral experience in cancer biology
? Working knowledge of basic cancer signaling pathways
? Independent, self motivated and innovative
? Excellent written and oral communication skills
? Experience in cell and biochemical assay development and analysis
? Excellent interpersonal skills; track record of success working collaboratively |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| PhD Medicinal/Synthetic Organic Chemist |
| * Ph.D. in synthetic organic or medicinal chemistry
* relevant post doc or up to 10 years of industrial experience
* Experience managing BS/MS chemists
* Proven track record of innovative project contributions including peer-reviewed publications
* Ability to work independently and ability to interact with a multidisciplinary team of medicinal chemists, biologists, pharmacologists and external collaborators.
* Experience with modern structure-based drug design and multi-parallel synthesis is a plus.
* Excellent oral / written communication and presentation skills
* Flexibility to work in a dynamic environment |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Pharmacogenetic Analyst |
| Competencies:
? Strong background in genetics and/or molecular biology
? Previous experience performing genetic association studies required
? Strong background in biostatistics and/or statistical genetics
? SAS programming a plus
? Proficiency working with and manipulating large data sets
? Broad scientific knowledge
? Experience in clinical development desirable
? Ability to work well in a team environment
? Excellent presentation and communication skills (essential)
? Strong publication record desirable
Education and professional experience:
PhD in genetics (or related fields) is required with experience performing genetic/genomic association studies. |
| Novartis Oncology |
na |
NE |
9/4/2010
|
| Pharmaceutical Technician |
| ? High school diploma or GED required. Associate?s degree in science or related field preferred.
? Must be able to demonstrate attention to detail, have organizational skills, good communication and interpersonal skills.
? Competency with basic math skills required.
? Supports and contributes as a team member to achieve team and company objectives.
? Participates in investigations and attends team meetings.
? Must be able to lift and move material drums of varying weights |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Pathways Cellular/Molecular Scientist (BS/MS) |
| Minimum requirements MS in Biochemistry, Molecular Biology, Cell Biology, with 5-10 years of laboratory research experience.
? Thoroughly familiar with culturing various mammalian cell lines and primary cells, generating stable cell lines, designing cell-based and biochemical assays, and executing small molecule screens.
? Outstanding molecular biology techniques including DNA cloning, DNA/RNA preparation and characterization (SB, NB, qPCR).
? Exceptional expertise in genetic screening with siRNA/shRNA/cDNA by conventional and viral transduction technologies.
? Proficient in various techniques of protein expression, purification and functional characterization (WB, Co-IP, ELISA, luciferase assay).
? Experience with fluorescent imaging, flow cytometry.
? Excellent communication skills and usage of data analysis software. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Patent Attorney |
| Minimum education: B.A., B.Sc. (or equivalent), chemistry, biochemistry or equivalent with strong understanding of medicinal chemistry in a biotech/pharma environment. M.S., Ph.D. or equivalent in organic or medicinal chemistry preferred.
J.D. or equivalent; Admission to at least one state bar; and Registered to practice before Patent Office.
? Expertise in local patent law; Detailed understanding of global patent systems (including but not limited to US, EP, JP and international systems), patent process, documentation and national and international patent office filing systems.
? Strong scientific background.
? Strong customer-service focus to build and sustain good working partnerships with key stakeholders and project teams.
? Effective analytical, presentation and communication skills.
? Demonstrated ability to work independently as well as collaboratively in a team.
? Well-developed research and critical thinking skills, and sound decision-making abilities, with attention to detail to produce consistently accurate work.
? Strong organization and time management skills with flexibility, creativity, resourcefulness to successfully prioritize and manage multiple, competing priorities simultaneously.
? Strong written and spoken communication in English is required. Proficiency in other languages, such as German, a plus. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Patent Agent II (Pharma Division) |
| ? Bachelor's Degree or higher in Chemistry, Biochemistry or other relevant scientific discipline.
? US Patent Agent Registration to practice
? Minimum 5 years' experience in patent prosecution in a corporate or law firm setting specific to chemical, pharmaceutical or healthcare industry
? Must be able to understand and apply basic patent law principles and procedures
? Excellent written and oral communication skills
? Ability to communicate clearly in a cross-functional and multinational environment and with employees of different levels within the company
? A small amount of travel to meetings and conferences may be required (about 5%). |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Paralegal |
| Education : Bachelor?s Degree(or equivalent in education and experience)
Paralegal Certificate (from a program approved by the American Bar Association)
Experience:
Minimum of 3 years of paralegal experience with expertise in litigation is required; Paralegal Certificate;
Experience in corporate, large law firm or government setting;
Experience in pharmaceutical industry preferred. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Outsourcing Manager |
| Minimum of Bachelor?s degree in business or Life Science or equivalent with a minimum of 5 years experience in contract negotiation and preparation and familiarity with legal terminology associated with the pharmaceutical industry or CROs. Strong negotiation skills/diplomacy. Strong oral and written communication skills. Strong analytical and problem solving skills. Strong interpersonal skills/team player. Customer focused
Fluent English (oral and written)
1. Capable of clear written and verbal expression of ideas, an active/proactive communicator
2. Ability to interact with a wide range of people and build strong positive relationships.
3. Potential for customer orientation awareness and focus
4. Basic knowledge of the Drug development process
5. Computer literacy
6. Excellent organizational skills |
| Novartis Oncology |
na |
CA |
9/4/2010
|
| Operator - Vacaville, CA Biopharmaceutical Operations |
| Requires handling of chemicals such as acids, alkalis, solvents and powdered media; Must be able to wear a negative pressure based respirator; Able to work in noisy environments that may exceed 80 decibels; May be required to lift up to 50 pounds multiple times in the work shift (e.g. 1-5 times in a hour); Requires pushing and pulling of equipment (e.g. drum dollies with 55 gallon drums or 500 liter portable tanks) throughout the work shift (e.g. 1-5 times in a period of 1 hour); Requires bending and reaching throughout the work shift in support of wide range of activities such as valve adjustment, fastening of hoses and/or connections and con-ducting cleaning activities; May require climbing up and down flights of stairs during the work shift (e.g. 1-4 times in a hour) as well as ascending a fixed or portable ladder to heights up to twenty feet; Requires walking / standing for extended periods (up to 6 hours) throughout the work shift; Must be able to enter confined spaces such as tanks and pits; Must be able to op-erate powered industrial trucks and/or motor vehicles throughout the work shift (e.g. driving periods up to 2 hours).
Minimum of 5 years experience with a H.S. diploma or 1 to 3 years experience with a Bachelors degree. Experience in GMP manufacturing or research and development is required. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Operational Alliances Representative |
| The ideal candidate will have a (life) science degree and enrolment in or completion of a business degree. The successful candidate will have at least three to five years experience in the pharma/biotech arena, and have a working understanding of the science related to it. Strong analytical and communication skills, and excellent skills in both prioritization and time management are required. The successful candidate will have a strong sense for urgency, be team player, and bring a creative approach to problem solving. Reliability, independence, and initiative are essential. Finally the candidate must have a genuine passion for science, and for finding new ways to perform his/her job better. |
| Novartis Oncology |
na |
IL |
9/4/2010
|
| Open Territory Specialist- Chicago IL |
| Minimum Education Required:
Bachelor's degree or equivalent
Minimum Experience Required:
1-2 years successful outside sales experience.
Preferred Level:
One (1) year contact lens sales/ophthalmic related sales/contact fitting experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel may be required.
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
CA |
9/4/2010
|
| Open Territory Specialist - Western US |
| Minimum Education Required:
Bachelor's degree or equivalent
Minimum Experience Required:
1-2 years successful outside sales experience.
Preferred Level:
One (1) year contact lens sales/ophthalmic related sales/contact fitting experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel may be required.
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
NY |
9/4/2010
|
| Oncology Sales Representative/Specialist - LI/Queens |
| Bachelor?s Degree 5 years of pharmaceutical sales experience At least 2 years of experience in oncology/urology/institutional/specialty sales. Computer literacy i.e., Word, Excel, PowerPoint Candidates must be self-motivated, possess a high degree of technical expertise, have exceptional selling skills, be team-oriented and must be familiar with the Oncology community. Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive advantage. Novartis is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
IA |
9/4/2010
|
| Oncology Sales Representative/Specialist - Iowa |
| Bachelor?s Degree 5 years of pharmaceutical sales experience At least 2 years of experience in oncology/institutional/specialty sales. Computer literacy i.e., Word, Excel, PowerPoint Candidates must be self-motivated, possess a high degree of technical expertise, have exceptional selling skills, be team-oriented and must be familiar with the Oncology community. Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive advantage. Novartis is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Oncology Pharmacologist BS/MS Scientist |
| B.A/B.S. or technical equivalent with expertise in in vivo physiology or pharmacology. Industry experience with oncology models is strongly preferred. Individuals with experience in molecular biology techniques are strongly encouraged to apply.
Candidates will be expected to possess:
? Hands on in vivo skills necessary to validate and implement rodent oncology models including dosing and tumor implantation techniques. Experience with models derived from primary patient samples a plus.
? Demonstrated ability to quickly learn and perform in new areas, implement new techniques and instrumentation.
? Meticulous laboratory approach, careful adherence to protocol and excellent lab notebook documentation
? Strong analytical and computer skills
? Strong oral and written communication skills
? Demonstrated team player. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Oncology Global Drug Development Fellow |
| Qualifications required
Medical Doctorate (MD) degree or equivalent is required.
Advanced knowledge in Oncology, Haematology, Endocrinology required. Completion of 2-4 years of post-MD training in above area required.
Fluent oral and written English. Any other language a plus.
Knowledge, Skills, and Experience desired
Involvement in patient care and demonstrated medical/scientific expertise in oncology and/or haematology
Exposure to or demonstrated interest and knowledge in pharmaceutical company research environment
Strong interpersonal, communication, and problem solving skills.
Demonstration of general understanding of drug development process including key processes involved in protocol development, clinical trial conduct, statistical analysis of trials, and regulatory environment,
Demonstration of ability to work within a team environment and across other functions
Mobility/Citizenship
Must be able to relocate to Basel, Switzerland or New Jersey, USA for a period of one year
Current residency/citizenship of an EU country is highly preferred.
Must be able to attain the appropriate work authorization for the US in a timely fashion.
For US and Switzerland, Novartis will apply on the candidate?s behalf. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Oncology Director/Sr. Director Global Medical Affairs |
| MD required. Board certified hematologist/oncologist preferred. Advanced knowledge of oncology required. Must have >5 years of demonstrated leadership and accomplishment in clinical trials and/or medical affairs (planning, executing, reporting clinical trials, leading medical affairs activities) in academia/pharmaceutical industry. Strong leadership, management, interpersonal, communication, negotiation, and problem-solving skills. Ability to think strategically. Organizational awareness (inter-relationship of departments, business priorities), and experience working on cross functional teams desired. Excellent written and oral communication skills, including presentation skills. Fluent oral and written English. Ability to interact effectively with external customers and internal stakeholders. Ability to travel, US and International. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Oncology Director Medical Affairs |
| MD with board-eligibility or certification in oncology or hematology preferred. Advanced knowledge of oncology required. Must have >2 years of demonstrated leadership and accomplishment in clinical trials and/or medical affairs (planning, executing, reporting clinical trials, leading medical affairs activities) in pharmaceutical industry. Team player attitude is necessary. Prior staff management experience is a plus. Ability to communicate and partner with global marketing and medical colleagues as well as study investigators. Ability to travel both domestically and internationally is required. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Onco Sr Dir Clinical Res Phys |
| The successful candidate will be required to have Board Certification in Oncology and Hematology with a minimum of 2+ year of industry experience managing clinical research or 5+ years of relevant medical/clinical experience.
? Experience in previous management and accountability for budget execution is desirable.
? Previous experience in collaborative interactions on clinical studies with investigators globally is very important
? Previous experience managing CRO interactions related to clinical study operations is highly desirable.
? Candidates should have demonstrated the capability for strategic planning along with operational skill and experience related to clinical research involving both single and multiple centers. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Onco Sr Dir Clinical Res Phys |
| The successful candidate will be required to have Board Certification in Oncology and Hematology with a minimum of 2+ year of industry experience managing clinical research or 5+ years of relevant medical/clinical experience.
? Experience in previous management and accountability for budget execution is desirable.
? Previous experience in collaborative interactions on clinical studies with investigators globally is very important
? Previous experience managing CRO interactions related to clinical study operations is highly desirable.
? Candidates should have demonstrated the capability for strategic planning along with operational skill and experience related to clinical research involving both single and multiple centers. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| NIBR Search Network, Application Manager |
| Qualifications:
? Advanced degree in Computer Science
? At least 3-5 years experience in Application Management
? Sound Knowledge of Search and Web Technologies
? At least 1 year of experience with the Fast ESP platform
? Strong communications and interpersonal skills
? Ability to work independently and as part of a team
? Work with different NITAS groups that work in close coordination with TMS e.g. Omega, Data and Middleware Management Services in RCP and the NITAS Help Desk in the US.
Reporting
The candidate will be part of the Text Mining Services Group, one of the IS (information services) groups in NITAS and will report to the Head of Text Mining Services located in Basel. The role is based in Cambridge, Massachusetts. The candidate will be a member of the NIBR Search team and work under the direction of the NIBR Search project leader. |
| Novartis Oncology |
na |
IL |
9/4/2010
|
| National Account Scientific Directpr |
| MD, PharmD, or PhD with 4 years Post-Doctoral experience required or relevant experience. Oncology experience required. Managed care & outcomes research experience preferred. Field based medical experience in the pharmaceutical industry preferred. Thorough knowledge of clinical medicine, the managed markets, pharmacoeconomics, disease management, and medical research. Excellent interpersonal communication and presentation skills, (including ability to network), strong personal integrity, teamwork abilities and a customer focus are necessary. Must possess a thorough understanding of the FDA, OIG, HIPAA, and GCP/ICH guidelines relevant to the pharmaceutical industry. Must be able to organize, prioritize, and work effectively in a constantly changing environment. Strong working knowledge of the organization of Microsoft Office Suite (Word, PowerPoint, Excel, Access). Ability to interface effectively with a variety of technical platforms for the collection, review, and dissemination of medical information. Demonstrated record of scientific/medical publication. Demonstrated knowledge of GCP practices and standards. Demonstrated technical expertise in oncology. |
| Novartis Oncology |
na |
AR |
9/4/2010
|
| National Account Manager-Walmart |
| ? Bachelors Degree or equivalent
? MBA Preferred
? 5+ years of field sales and industry related experience.
? Proficient computer skills in MS Office and database usage.
? Previous Walmart or Sam?s Club Experience preferred |
| Novartis Oncology |
na |
MN |
9/4/2010
|
| National Account Manager-Target |
| ? Bachelors Degree or equivalent
? MBA Preferred
? 5+ years of field sales and industry related experience.
? Proficient computer skills in MS Office and database usage.
? Previous Traget sales experience preferred |
| Novartis Oncology |
na |
OH |
9/4/2010
|
| National Account Manager-Kroger |
| ? Bachelors Degree
? Kroger account management experience
? 5+ years of field sales and industry related experience.
? Proficient computer skills in MS Office and database usage.
? Travel Approximately 35%.
This is a home based position in the Cincinnati area. |
| Novartis Oncology |
na |
RI |
9/4/2010
|
| National Account Manager-CVS |
| -Bachelors Degree or equivalent
- 5+ years of field sales and CPG industry related experience.
- 7 + years key account management in Consumer Products
- Proficient computer skills in MS Office and database usage.
- Proficient in working use of computer systems including Adesso, SAP, SFS |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Muscle Regenerative Medicine Research Investigator (Ph.D) |
| The candidate should have a Ph.D. in an appropriate discipline, greater than 3 years post-doctoral experience and demonstrated expertise in a fields of regenerative medicine, cell and molecular biology. Expertise in modeling complex biology in vitro and ex vivo is required and we are particularly interested in candidates with a strong background in the area of skeletal or cardiac muscle biology. The candidate should have excellent communication skills and an ability and desire to work in a highly team oriented environment. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Multiple Sclerosis Sr Nurse Educator - Atlanta, GA - MC1ENB |
| Education/Experience:
? RN with a four year Bachelors degree is required
? RN (ADN) with MS Certification in lieu of Bachelors degree
? Minimum 3-5 years nursing experience necessary
? Multiple Sclerosis/Neurology experience preferred, but not required
? Ability to manage multiple tasks and adapt to changing environments/situations required
? Excellent communication/presentation skills are needed
? Sales experience and/or displayed leadership skills a plus
? Overnight travel required
This position covers multiple territories. Overnight travel is required ranging from 10% to 40%
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive advantage. Novartis is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
WA |
9/4/2010
|
| Multiple Sclerosis Regional Institutional Marketer - West |
| This person should have strong marketing experience and proven success in the areas of
KOL development, medical marketing and meeting + event tactical execution. Specific experience in marketing multiple sclerosis products is a strong plus. Business and/or medical, sciences education with concentration on marketing is preferred (PharmD or MBA a plus). Sales ,sales leadership and account management experience are also highly favorable. Solid strategic thinking skills and analytical skills are essential as well as strong senior management communication skills and sales force communication. The ideal candidate will have the ability to bridge marketing and science and the ability to manage a heavy workload common to a priority brand.
The applicant must possess a high level of analytical and conceptual ability in order to provide strategic focus to the brand, and demonstrate a proven track record of strong execution and results. Additional requirements include the ability to lead and manage teams across functional areas. 40-50% travel is required.
Preferred Skills:
? Deep understanding of the local MS market dynamics
? Experience/competencies in marketing
? Managed Markets experience |
| Novartis Oncology |
na |
WA |
9/4/2010
|
| Multiple Sclerosis Area Sales Manager - Seattle, WA MW1F |
| ? Bachelor's degree (preferably in Life Sciences, Pharmacy, or Business related discipline)
? 3 or more years of pharmaceutical sales experience including 2 yrs. Specialty experience
? At least 2 years of pharmaceutical Specialty Sales Management experience.
Preferred Requirements:
? Strong ability to collaborate and work cross-functionally within a matrix environment.
? Demonstrated ability to increase sales through facilitating relationships between Managed Care institutions.
? Demonstrated ability to lead and inspire a group towards meeting and exceeding objectives.
? Strong leadership, planning and organization, and problem solving and decision making skills.
? Specialty sales experience and/or hospital/institutional experience required, MS experience preferred. |
| Novartis Oncology |
na |
MD |
9/4/2010
|
| MS Specialist - Silver Spring, MD ME1F1B |
| * Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline
* Minimum of 5 years of successful pharmaceutical sales experience.
* 2 years of which must be in Institutional or Specialty Sales (preferably with Neurologists)
* Demonstrated ability to work with Academic customers
* Previous MS Sales experience & familiarity with the Neuroscience/MS community is highly preferred.
* Internal candidates must be in their current position for at least two years.
Additional Information:
Candidates need to be motivated, results-oriented and have a high degree of technical expertise, exceptional selling skills, and must have outstanding skills in the areas of communication, organization, decision making and tactical execution. Must demonstrated collaboration, relationship building and customer service competencies.
Excellence in required skills: interpersonal communication, organization & prioritization, presentation skills, decision making, tactical execution & computer literacy.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive advantage. Novartis is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
PA |
9/4/2010
|
| MS Sales Specialist - Wilkes-Barre, PA ME1D2A |
| * Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline
* Minimum of 5 years of successful pharmaceutical sales experience.
* 2 years of which must be in Institutional or Specialty Sales (preferably with Neurologists)
* Demonstrated ability to work with Academic customers
* Previous MS Sales experience & familiarity with the Neuroscience/MS community is highly preferred.
* Internal candidates must be in their current position for at least two years.
Additional Information:
Candidates need to be motivated, results-oriented and have a high degree of technical expertise, exceptional selling skills, and must have outstanding skills in the areas of communication, organization, decision making and tactical execution. Must demonstrated collaboration, relationship building and customer service competencies.
Excellence in required skills: interpersonal communication, organization & prioritization, presentation skills, decision making, tactical execution & computer literacy.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented, performance driven people. All of which makes us one of the most rewarding employers in our field. We're committed to peak performance, improving the quality of life, and embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive advantage. Novartis is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
DC |
9/4/2010
|
| MS Sales Specialist - Washington, DC/Silver Spring, MD ME1F2C |
| * Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline
* Minimum of 5 years of successful pharmaceutical sales experience.
* 2 years of which must be in Institutional or Specialty Sales (preferably with MS products or Neurologists)
* Demonstrated ability to work with Academic customers
* Previous MS Sales experience & familiarity with the Neuroscience/MS community is highly preferred.
* Internal candidates must be in their current position for at least two years.
Additional Information:
Candidates need to be motivated, results-oriented and have a high degree of technical expertise, exceptional selling skills, and must have outstanding skills in the areas of communication, organization, decision making and tactical execution. Must demonstrated collaboration, relationship building and customer service competencies.
Excellence in required skills: interpersonal communication, organization & prioritization, presentation skills, decision making, tactical execution & computer literacy.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented, performance driven people. All of which makes us one of the most rewarding employers in our field. We're committed to peak performance, improving the quality of life, and embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive advantage. Novartis is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
VA |
9/4/2010
|
| MS Sales Specialist - Richmond, VA ME1BF2D |
| * Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline
* Minimum of 5 years of successful pharmaceutical sales experience.
* 2 years of which must be in Institutional or Specialty Sales (preferably with Neurologists)
* Demonstrated ability to work with Academic customers
* Previous MS Sales experience & familiarity with the Neuroscience/MS community is highly preferred.
* Internal candidates must be in their current position for at least two years.
Additional Information:
Candidates need to be motivated, results-oriented and have a high degree of technical expertise, exceptional selling skills, and must have outstanding skills in the areas of communication, organization, decision making and tactical execution. Must demonstrated collaboration, relationship building and customer service competencies.
Excellence in required skills: interpersonal communication, organization & prioritization, presentation skills, decision making, tactical execution & computer literacy.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented, performance driven people. All of which makes us one of the most rewarding employers in our field. We're committed to peak performance, improving the quality of life, and embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive advantage. Novartis is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
PA |
9/4/2010
|
| MS Sales Specialist - Pittsburgh South, PA ME1E2C |
| * Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline
* Minimum of 5 years of successful pharmaceutical sales experience.
* 2 years of which must be in Institutional or Specialty Sales (preferably with Neurologists)
* Demonstrated ability to work with Academic customers
* Previous MS Sales experience & familiarity with the Neuroscience/MS community is highly preferred.
* Internal candidates must be in their current position for at least two years.
Additional Information:
Candidates need to be motivated, results-oriented and have a high degree of technical expertise, exceptional selling skills, and must have outstanding skills in the areas of communication, organization, decision making and tactical execution. Must demonstrated collaboration, relationship building and customer service competencies.
Excellence in required skills: interpersonal communication, organization & prioritization, presentation skills, decision making, tactical execution & computer literacy.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented, performance driven people. All of which makes us one of the most rewarding employers in our field. We're committed to peak performance, improving the quality of life, and embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive advantage. Novartis is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
CA |
9/4/2010
|
| MS Sales Executive Specialist - San Francisco, Ca. - Overlay MW1E2E |
| * Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline
* Minimum of 5 years of successful pharmaceutical sales experience.
* 2 years of which must be in Institutional or Specialty Sales (preferably with Neurologists)
* Demonstrated ability to work with Academic customers
* Previous MS Sales experience & familiarity with the Neuroscience/MS community is highly preferred.
* Internal candidates must be in their current position for at least two years.
Additional Information:
Candidates need to be motivated, results-oriented and have a high degree of technical expertise, exceptional selling skills, and must have outstanding skills in the areas of communication, organization, decision making and tactical execution. Must demonstrated collaboration, relationship building and customer service competencies.
Excellence in required skills: interpersonal communication, organization & prioritization, presentation skills, decision making, tactical execution & computer literacy.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive advantage. Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Molecular/Cell Biology Research Associate (BS/MS) |
| B.S/M.S. degree with over 3 years of lab experience and strong background in cell biology, biochemistry and molecular biology. Previous experience in the study of innate immunity is highly desirable. Experience with large dataset analysis is a plus. The candidate is expected to possess strong problem solving and analytical skills, and be capable of independent, creative thinking. Excellent communication and organization skills are required. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Molecular Phenotyping Scientist |
| Applicants should hold a BS degree in biology (or related fields) with 2 plus years experience as research histologist in the bio-pharmaceutical industry or biomedical research. A very good understanding and practical experience of special histology techniques and immunohistochemistry applied to pre-clinical research is essential. Excellent knowledge of molecular biology concepts applicable to research histology in order to select appropriate reagents and assay design is highly desirable. An excellent capacity and adaptability to learn new techniques under the direction of more senior laboratory peers is required. Previous experience in digital slide scanning and image analysis applied to tissue sections is a plus. Excellent organizational skills in daily laboratory activities are essential. Good interpersonal skills and capacity to conduct laboratory activities in a dynamic cross-functional research environment is essential. Excellent computer skills with daily experience with Microsoft Office environment are also required. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Molecular Pathways Investigator (Ph.D) |
| Ph. D. degree with 1- 3 years of postdoctoral training and with strong background in cell biology, biochemistry and molecular biology. Previous experience with identification and progression of biological targets is a plus. The candidate is expected to possess strong problem solving and analytical skills, and be capable of independent, creative thinking. Excellent communication and organization skills are required. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Molecular Pathway Biology Research Scientist (BS/MS) |
| BS or MS scientist with 3-5 years of laboratory research experience.
? Thorough familiarity with culturing various mammalian cell lines and primary cells, generating stable cell lines, designing cell-based and biochemical assays, and executing small molecule screens.
? Outstanding molecular biology techniques including DNA cloning, DNA/RNA/protein isolation and characterization.
? Expertise in genetic screening with siRNA/shRNA/cDNA by conventional and viral transduction technologies.
? Excellent communication skills and usage of data analysis and repository software.
? Eagerness and flexibility to learn new techniques, a positive team orientation, and genuine scientific curiosity are a must. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Molecular Pathologist, Investigative Toxicology |
| Education
? MD or DVM, board-certified pathologist or equivalent
and
? PhD or equivalent scientific records in life sciences
Experience
? Extensive operational knowledge of gene expression analysis from tissues
? Proficient data interpretation techniques applicable to toxicology
? Knowledge in toxicology and/or toxicologic pathology
? Significant scientific experience working in molecular pathology or molecular toxicology
? Hands-on experience in immunohistochemistry/in situ hybridization,image analysis, and gene expression profiling
? Excellent data summarization: used to presenting clearly and simply complex data or phenomena
? Excellent oral and written English communication skills. Able to present and defend data and influence the decision process regarding study design
? Experience organizing labs
? A results-driven self-starter and decision taker; open, confident and persuasive, succeeding through influence
? A creative and innovative approach with a sharp and objective intellect, experienced in balancing big picture thinking with detailed analysis
? Strong cooperative team player, ability to be flexible and adapt to a changing environment
? A commercial outlook; used to helping a business achieve its objectives
? Well developed interpersonal skills
? Good planning, prioritisation, problem solving and organisational skills
? Resilient, energetic and enthusiastic; responding constructively to challenging new ideas and inputs |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Molecular and Cellular Biology Research Scientist (BS/MS) |
| ? B.S/M.S. in Biochemistry, Cell Biology or Molecular Biology
? Minimum 5 years experience in biochemistry, mammalian cell biology working with various cell lines and/or cell signaling mechanisms
? Previous experience with stable cell line production, design and analysis of cell-based assays, transfection and viral transduction technologies and RNAi techniques is required.
? Proficiency in the use of molecular biology and protein biochemistry technologies, e.g. DNA cloning, Real-time PCR, protein-protein interaction, and enzymatic assays is preferred.
? Familiar with different technologies to monitor cellular events (proliferation assays, high content imaging, technologies to monitor the state of signaling molecules in cellular extracts).
? Must be highly motivated, team-oriented, and have excellent interpersonal and communication skills. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Mgr/Associate Director, Audit and Monitoring (Ethics and Compliance) |
| B.A. degree; experience in audit; CPA and/or CFE certification preferred.
KNOWLEDGE AND SKILL REQUIREMENTS:
1. Knowledge of audit techniques including risk analysis identification skills.
2. 5-10 years experience with at least 3 years in the pharmaceutical industry conducting complex, sensitive and essential (ad-hoc and required) audit and monitoring activity related to pharmaceutical fraud and abuse and regulatory non-compliance in order to identify individual conduct issues as well as overall program enhancement opportunities (e.g., policy, training, etc).
3. Strong interpersonal, communication, and presentation skills. Requires political savvy and the ability to take difficult or unpopular positions when necessary to protect the company.
4. Visibility requires maintaining an even temper and treating all persons with respect to project a positive image at all times despite stress or other circumstances.
5. Solid knowledge of Federal health care regulations, FDA and OIG laws/guidelines in relation to compliance program administration within the pharmaceutical industry.
6. Candidate must have the proven ability to evaluate trends, organize and conduct multiple, simultaneous audit and monitoring initiatives, deal tactfully with others, prepare accurate and sound reports, and coordinate with many cross-functional stakeholders to achieve identified outcomes.
7. Ability to travel 40%. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Mgr, CMC |
| Education:
Minimum BS or BA, MS in Life Science: Pharmacist preferred, or equivalent
Experience:
1 (Specialist) to 2/3+ (Senior Specialist) and 5 + (Manager) years in CMC Regulatory Affairs |
| Novartis Oncology |
na |
PR |
9/4/2010
|
| Mgr Purchasing |
| Demonstrate experience in sourcing. The individual should have thorough knowledge of sourcing in a GMP environment. The individual should have a working knowledge of sourcing methods. Requires skills to plan, schedule and coordinate the sourcing projects with minimum supervision. |
| Novartis Oncology |
na |
CA |
9/4/2010
|
| Mfg Process Engineer - Vacaville, Calif |
| BS in Chemical, Biochemical, or Mechanical Engineering, preference in Chemical/Biochemical Engineering.
Written and spoken English
Up to 5 years in a commercial manufacturing environment |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| MES Engineer |
| Minimum Education Required:
BS in Engineering or Computer Science.
Minimum Experience Required:
Five years experience with Plant Floor Manufacturing Execution System (MES) application, including the de-velopment of electronic batch records.
Two years experience with Wonderware MES Solutions.
Two years experience using Microsoft Visual Studio 2005 and SQL Reporting Services to develop reports and ASP.NET Web applications.
Five years experience with Relational Databases. Prior experience with development and maintenance, especially Oracle 10g and Microsoft SQL is required.
Knowledge of industry standard methods/middleware including OPC and XML.
Experience working with FDA regulated industries and 21 CFR Part 11 Compliance. Understanding of GxP regulations and computer validation principles is required.
Experience following the SDLC (Software Development Life Cycle)
Proven analytical/problem solving skills; demonstrated ability to dig into problems at detail level and reconcile system anomalies/problems with supporting data.
Experience with Allen Bradley PLCs is a plus.
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Medicinal Chemistry Associates/Scientists (BS/MS) |
| Multiple positions exist at all levels for candidates with the following minimum qualifications. B.S. in Chemistry or M.S. degree with at least 1 year experience in the synthesis and characterization of organic compounds. Experience with common spectroscopy (NMR, IR, UV, MS) and analytical techniques required. Experience with chromatography purification systems required. Good written and oral communication skills are required for effective drug discovery team participation. For faster consideration, please provide research summary when submitting resume. NIBRIERP |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Medical Scientific Expert |
| Education: MD required with unique knowledge for successful clinical program development and execution required.
Languages: Fluent English (oral and written)
Experience:
? Advanced medical/scientific writing and communication skills.
? Proven ability to interpret, discuss and represent efficacy and safety data relating to the assigned area.
? Proven ability to work both independently or in a cross functional team setting, including a matrix environment.
? Clinical research experience preferred.
? Medical and/or scientific expertise within a disease area preferred. Preference for previous experience with Heart Failure or Thrombosis focused work. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Medical Science Liaison (MSL) Hematology - New Jersey |
| Position will be filled at level commensurate with experience. Advanced scientific degree required (MD, PhD, or PharmD highly preferred). Minimum of 5 years Oncology experience with a strong current working knowledge of Oncology required. Teaching experience preferred. Previous pharmaceutical industry experience preferred. Thought leader development experience is a plus. Knowledge of treatment guidelines, clinical research processes, FDA regulations and OIG guidelines is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important external customers, including medical thought leaders, academic institutions, large group practices, medical directors and pharmacy directors is required. Must be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Must be a strong team player who can effectively interface cross-functionally with Novartis clinical and commercial personnel. Working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel) and associated hardware is required. The position is associated with approximately 60% travel. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Medical Information Mgr/Associate Director US MIC Multiple Sclerosis |
| This position will be filled at a level commensurate with experience.PharmD, healthcare-related PhD, or MD is required with significant industry or related medical information experience preferred. Post-graduate specialty training is desirable. Customer-oriented approach and ability to effectively work in cross-functional teams. Strong knowledge of medical terminology, pathophysiology, pharmacology, pharmacotherapeutics, and laboratory diagnostic tests. Knowledge of drug information processes and adverse event reporting regulations a must. Computer literacy is required. Excellent verbal, written, and telephone communication skills. At least 1 to 3 years of experience in a drug information setting is preferred. Previous experience in the Multiple Sclerosis Therapeutic Area is preferred. Ability to travel (approximately 10%). |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Medical Director/Senior Medical Director, Psychiatry, US Medical |
| A MD or DO degree with 3-5 years of pharmaceutical industry experience is required; Board Certification/Eligibility in Psychiatry and clinical/research background in Psychiatry would be a plus.
? Experience in managing clinical trial conduct for psychiatric disorders is essential.
? Firm working knowledge of GCP, scientific and clinical methodology, protocol design, project management and regulatory requirements for clinical studies designated for review by regulatory authorities.
? Medical Affairs and U.S. marketing experience, to include a well documented history in medical development of Psychiatric therapeutics and of bridging proactive relationships among product development, clinical development and marketing teams.
? A well-established network within the medical research community that will attract high-caliber professionals into the Novartis organization.
? Proven ability to build productive relationships and teams internally and externally, and the ability to develop high potential subordinates into leadership roles.
? Reputation as an open, available and transparent communicator.
? Strong leadership and organizational skills; demonstrated personnel management capabilities.
? Excellent oral and written communication skills.
? Experience leading large projects/organizations.
? Ability to travel (U.S. and European; 20-25% annually. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Medical Dir/Sr Medl Dir,Primary Care, US Medical(Arthritis/Immunology) |
| ? A MD or DO degree with 3-5 years of pharmaceutical industry experience is required; Board Certification/Eligibility in Internal Medicine and clinical/research background in rheumatology would be a plus.
? Experience in managing clinical trial conduct for rheumatologic disorders is essential.
Firm working knowledge of GCP, scientific and clinical methodology, protocol design, project management and regulatory requirements for clinical studies designated for review by regulatory authorities.
? Medical Affairs and U.S. marketing experience, to include a well documented history in medical development of rheumatology therapeutics and of bridging proactive relationships among product development, clinical development and marketing teams.
? A well-established network within the medical research community that will attract high-caliber professionals into the Novartis organization.
? Proven ability to build productive relationships and teams internally and externally, and the ability to develop high potential subordinates into leadership roles.
? Reputation as an open, available and transparent communicator.
? Strong leadership and organizational skills; demonstrated personnel management capabilities.
? Excellent oral and written communication skills.
? Experience leading large projects/organizations.
?Ability to travel (U.S. and European; 20-25% annually). |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Medical Dir/Sr Medical Director US Medical NSO (Multiple Sclerosis) |
| A MD degree with 3-5 years? pharmaceutical industry experience is required; Board Certification/Eligibility in Neurology and clinical/ research background in Multiple Sclerosis will be a plus.
? Experience in managing clinical trial conduct for neurological disorders and Multiple Sclerosis is essential.
? Firm working knowledge of GCP, scientific and clinical methodology, protocol design, project management and regulatory requirements for clinical studies designated for review by regulatory authorities.
? Medical Affairs and U.S. marketing experience, to include a well documented history in medical development of Multiple Sclerosis/ Neuroscience therapeutics and of bridging proactive relationships among product development, clinical development and marketing teams.
? A well-established network within the medical research community that will attract high-caliber professionals into the Novartis organization.
? Proven ability to bu | |
