| Miltenyi Biotec Inc. |
Auburn |
CA |
11/19/2009
|
| Marketing Product Manager - Auburn, CA |
| Bachelor’s or graduate degree in the life sciences, or MBA preferred. Must have in-depth technical knowledge and 2 to 5 years of experience in science field related to product line marketing; or equivalent combination of education and experience.
We offer a competitive salary and excellent benefits package. There is no relocation associated with this position. EOE/AA
https://home.eease.com/recruit/?id=229953 |
| Miltenyi Biotec Inc. |
|
|
11/20/2009
|
| Technical Sales Consultant |
| Ph.D., M.S. or B.S. degree from a four-year college or university and two to four years experience in the life sciences environment; or equivalent combination of education and experience. Immunology and/or Molecular Biology background is preferred, and Ph.D. is highly desirable.
Other Requirements: Must possess a valid driver’s license, evidence of insurance / insurability and ability to receive appropriate clearance to access restricted government accounts.
We offer a competitive salary, commission, car allowance, and excellent benefits package. There is no relocation associated with this position. EOE/AA
To apply, go to: https://home.eease.com/recruit/?id=367955
|
| Southern Research Institute |
Frederick |
MD |
11/20/2009
|
| Molecular Biologist |
| Currently, our Frederick, Maryland facility is seeking to fill an immediate opening for an advanced individual in the technical support group. Candidate must have a strong background in molecular biology and must be experienced in mammalian tissue culture, RT-PCR, DNA and RNA isolation, recombinant DNA cloning, ELISA, plaque assays and other molecular and immunological techniques. Experience in developing and trouble-shooting molecular assays to detect infectious agents required. Must be able to work independently and develop assays with little guidance using reference materials. Good organizational and computer skills, in addition to a meticulous approach to laboratory experimentation required. Must be able to clear medical and vaccination requirements to work in BSL-3 and be cleared to work with select agents. GLP experience a plus. BS in Biological Science or related field required. MS preferred.
This position will support a variety of contracts, including a multi-million dollar NIAID Biodefense contract focusing on development of various animal models for select agents that includes the evaluation of new therapeutic and vaccine approaches. Primary duties will include optimizing current molecular assays and developing new assays for virus detection in a variety of samples obtained from animals immunized and/or challenged with poxviruses, VEE/WEE, influenza, and other infectious agents. This position will involve handling infectious materials under BSL-2/BSL-3 safety conditions. The position will also be responsible for maintaining general laboratory reagents and supplies. This position must be able to communicate clearly with other members of the scientific staff and be willing to gain further experience through attending conferences, workshops and training courses. This position must be able to work with team members at all levels and all reporting structures within the organization to ensure successful completion of study protocols.
Work Environment & Conditions: Individuals who will enter BSL-2/BSL-3 labs must: satisfactorily complete medical requirements; obtain applicable vaccinations; pass and maintain in depth security and background checks, including clearance to handle select agents; wear required PPE; and must have effective communication skills. All offers of employment (and continued employment) are subject to drug testing.
Applications must be made online at http://www.southernresearch.org / for position sr-02193
|
| Southern Research Institute |
Frederick |
MD |
11/20/2009
|
| Scientific Project Leader for Emerging Pathogens |
| Seeking qualified candidate with a PhD in life sciences discipline, MD, or DVM with a minimum of eight years prior experience managing NIH grants, contracts or projects in the biotech or pharmaceutical industry environment. Must be proficient in project management methodologies, have demonstrated success in generating/developing funding streams through successful proposal submissions; an outstanding publication record and documented combination of education, experience, and training to qualify as a study director within specified programs. Must be able to lead execution of large complex projects involving multiple technical staff at varying levels of expertise. Must be able to respond quickly to new funding opportunities while, at the same time, provide support to existing projects. Prior successful experience in a Contract Research Organization is highly preferred. Qualified candidate must be able to positively interact and communicate with individuals across the organization at all levels and positively engage current and potential funding sponsors within the government and private sector. Candidate must be able to work in a team environment and be capable of supporting and participating in related ongoing project lead by others. Must be able to be able to collaborate with others to accomplish a common goal.
Prior documented experience working in infectious disease research, particularly virology, immunology, biomarkers, and animal models (small animal or NHP models) of infectious diseases. Well known standing in the field of human pathogenic viruses preferred. Experience in respiratory viruses, antiviral therapeutics, or vaccine discovery and development preferred. Prior GLP experience preferred. Must be able to obtain clearance for select agents. This position will work in a BSL2 and BSL3 plus environment and therefore must be able to meet the medical and vaccination requirements.
This position is responsible for obtaining funding for and ensuring the successful execution of projects awarded. This position, as the study director of awarded projects, is responsible for the overall technical conduct of the study; interpretation, analysis, documentation, and reporting of results; issuance of study protocols and amendments; adherence to study protocols and amendments; following GLP practices; meeting all contract deliverables; and maintaining a positive relationship with the client. This position also ensures the quality of the product or service delivered; manages project budget and risk factors; and uses project management methodologies to ensure that projects are managed effectively. We operate in a matrix environment. This position may or may not have direct reports. Regardless of direct reporting technical staff, this position is responsible for the supervision of any/all individuals supporting the project to ensure high quality outcomes. This position is responsible for providing performance feedback to individuals supporting projects through informal and formal performance management processes. This position coordinates necessary technical talent with other project leaders and supervisors to ensure project needs are met. This position trains and develops others as necessary, provides mentoring and coaching, and seeks input from others when necessary. Prior supervision/leadership experience helpful. This position will report to the Director of Infectious Disease Research or the Program Leader.
Work Environment & Conditions: Individuals who will enter BSL-2/BSL-3 labs must: satisfactorily complete medical requirements; obtain applicable vaccinations; pass and maintain in depth security and background checks, including clearance to handle select agents; wear required PPE; and must have effective communication skills. All offers of employment (and continued employment) are subject to drug testing.
Applications must be made online at http://www.southernresearch.org / for position sr-02194
|
| Miltenyi Biotec Inc. |
Auburn |
CA |
11/20/2009
|
| Technical Support Scientist |
| Ph.D. in Immunology, Molecular Biology or similar field with 1-3 years experience in life sciences environment; or equivalent combination of education and experience. Flow cytometry experience is a must.
We offer a competitive salary and excellent benefits package. There is no relocation associated with this position. EOE/AA
To apply, go to: https://home.eease.com/recruit/?id=370281 |
| Morphotek®, Inc. |
Exton |
PA |
11/19/2009
|
| Director, Quality Assurance, Pilot Plant |
| Scope Measures
Oversight of all quality assurance functions within the pilot plant, with a total headcount of ~ 15 persons over the next three years. Considerable decision making capability with regard to ensuring quality is built into development and production processes and that all regulatory and procedural requirements are adhered to.
Knowledge/Skills/Abilities Required
Graduate level degree in quality and/or biological sciences or related subjects is preferable. BS degree required.
Must have knowledge of FDA, EMEA and JP regulations as they pertain to building design, aseptic process requirements and development of antibody-based biotherapeutics.
|
| Morphotek®, Inc. |
Exton |
PA |
11/19/2009
|
| Sr. Scientist - Pharmacology |
| Job Requirements and Qualifications
Education: PhD with training in pathology, cell biology or related fields, expertise in oncology preferred but not required.
Must have at least 5 years experience in biotech/pharmaceutical industry.
Strong experimental skills in human disease model development, mammalian tissue culture, vector transduction and imaging-related technology.
Oncology experience is preferred. Experience in IHC is a plus.
A thorough understanding of molecular oncology and immunology.
Demonstrated experience in in vivo human disease model and an excellent publication record.
Supervisory experience preferred.
Excellent organizational, time management, communication, and interpersonal skills.
Strong oral and written skills, and experience maintaining a record of studies in the form of notebooks, technical reports, summaries, protocols, and quantitative analyses.
Other Information
Special Information (Travel required, physical requirements, on-call schedules, and etc.):
Some travel may be required.
|
| Morphotek®, Inc. |
Exton |
PA |
11/19/2009
|
| Senior Clinical Quality Assurance Specialist |
| Job Requirements and Qualifications
BA/BS degree in biological sciences, nursing or related discipline, or equivalent experience required
Strong knowledge of government regulations, guidelines and standards for investigation of new pharmaceutical products is required
Experience in QA audits of Clinical Investigators
Experience in QA audits of Clinical documents associated with clinical trials
Experience in system/process audits
Experience in development of SOPs
Working knowledge and understanding of drug development and global clinical regulatory environment
Ability to manage multiple projects
Effective organizational skills
Effective team player and detail oriented
Strong attention to detail, good organizational skills, ability to work independently
Solid oral and written communication skills with ability to communicate effectively and professionally with medical personnel
Knowledge Requirements:
Knowledge of the code of federal regulations, European Directives, ICH/GCP practices. The candidate will also have a working knowledge of clinical auditing processes. Previous participation in regulatory inspections is a plus.
Experience:
A minimum of 3-5 years working experience as a clinical quality assurance auditor.
Other Information
Special Information (Travel required, physical requirements, on-call schedules, and etc.):
Travel 25-35%
|
| Morphotek®, Inc. |
Exton |
PA |
11/19/2009
|
| Associate Director, Technical Quality Operations |
| Job Requirements and Qualifications
Education: Graduate level degree in biological sciences or related subjects. Ph.D. preferred
Knowledge Requirements:
Knowledge of protein chromatography, mammalian cell culture and expression systems
Strong working knowledge of cGMP
Excellent written and verbal communication
Excellent interpersonal skills required, in addition to analytical problem solving, the ability to set priorities and achieve goals, and strategic thinking
Ability to manage multiple projects
Willingness and ability to assist all team members to achieve project goals
Working knowledge of Microsoft Office (Word, Excel, and Access).
Technical writing
Experience:
Minimum 10 years experience with cell culture, microbial fermentation and purification processes, scale up strategies and analytical testing of biologics, with at least 1-2 years of antibody manufacturing experience in an FDA regulated environment. Experience performing Quality Assurance functions such as SOP and protocol writing, batch record review, and investigations into deviations and out of specification results is highly preferred.
Other Information
Special Information (Travel required, physical requirements, on-call schedules, and etc.):
Travel 20-30%
Normal office environment
Laboratories on Site: Use of lab coat and safety goggles, as applicable
|
| Morphotek®, Inc. |
Exton |
PA |
11/20/2009
|
| Scientist, Bioanalytical Development |
| Knowledge/Skills/Abilities Required
• BS/MS with 5-7 yrs or PhD with 0-2 yrs relevant experience required.
• In-depth knowledge and understanding of bioanalytical assays for protein macromolecules with strong scientific and technical skills in method development and validation.
• A minimum of 5 years of hands-on experience in the development and/or validation of quantitative ligand binding and immunogenicity assays for biologics (e.g. antibodies, proteins or peptides).
• Well versed in current regulatory guidance and industry practices for development and validation of bioanalytical methods for large molecule biologics.
• Excellent verbal and written communication skills.
• Experience in GLP and/or clinical regulatory compliance is desired.
• Strong analytical skills, and a demonstrated ability to work both independently and in a team setting required.
|
| New England Research Institute |
Watertown |
MA |
11/19/2009
|
| Data Manager II |
|
•BA/BS degree in public health, computer science or related field. Masters degree preferred
•2-4 years experience with electronic data capture systems, spreadsheets and word. Experience with Oracle and SQL preferred
•Knowledge of statistical software
such as SAS helpful;
•Proven ability to coordinate and monitor the quality of data
•Experience developing training and procedures manuals;
•Previous experience in a clinical trial environment is preferred.
If interested, please send your resume and cover letter to Human Resources at humanresources@neriscience.com or visit us at www.neriscience.com
__
NERI is an Equal Opportunity/Affirmative Action Employer M/F/D/V
|
| New England Research Institute |
Watertown |
MA |
11/19/2009
|
| Senior Clinical Data Manager II |
|
•BA/BS plus 5 years of data management experience or MPH plus 3 years of data management experience preferred;
•Must have prior experience in clinical trails and comprehensive knowledge of FDA, ICH, GCP, 21 CFR Part 11 regulatory requirements;
•Experience with data management software such as Inform, E-Clinical, Clinical, ClinTrial or other DMS packages;
•Ability to coordinate and monitor the quality of research data collected;
•Demonstrated GCDMP knowledge required, CDM certification preferred;
•Strong verbal and written communication and Must be team oriented.
If interested, please send your resume and cover letter to Human Resources at humanresources@neriscience.com or visit us at www.neriscience.com
__
NERI is an Equal Opportunity/Affirmative Action Employer M/F/D/V
|
| New England Research Institute |
Watertown |
MA |
11/19/2009
|
| Senior Data Manager |
|
•BA/BS plus 5 years of data management experience. MPH plus data management experience preferred.
•Must be proficient in MS Office applications;
•Strong verbal and written communication;
•Ability to multi-task;
•Must be team oriented;
•Experience with data management software such as Inform, E-Clinical, Clinical, ClinTrial or other DMS packages;
If interested, please send your resume and cover letter to Human Resources at humanresources@neriscience.com or visit us at www.neriscience.com
NERI is an Equal Opportunity/Affirmative Action Employer M/F/D/V |
| New England Research Institute |
Watertown |
MA |
11/19/2009
|
| Senior Biostatistician |
|
•PhD required: Minimum degree of MS in Statistics with PhD in appropriate life science (eg; biology, zoology) or MS in life science with PhD in statistics;
•Experience in designing assay development experiments and/or analyzing lab data working as a statistician;
•Ability to write sections of collaborative manuscripts and/or full papers on study design and methodological issues;
•Excellent communication skills---both oral and written;
•Minimum 7 years of experience beyond PhD program;
•Experience working in clinical research and working on project teams;
•Ability to mentor junior level statisticians;
•Ability to communicate directly with investigators both inside and outside of NERI on matters related to study design and results, select appropriate statistical methods and conduct complex analyses.
If interested, please send your resume and cover letter to Human Resources at humanresources@neriscience.com or visit us at www.neriscience.com
__
NERI is an Equal Opportunity/Affirmative Action Employer M/F/D/V
|
| The HR Team, LLC |
Washington DC |
DC |
11/19/2009
|
| DDMAC Regulatory Professionals |
|
| Miltenyi Biotec Inc. |
|
|
11/20/2009
|
| Field Service Engineer: Mid-Atlantic Southeast |
|
| Strategic Diagnostics Inc. |
Newark |
DE |
11/19/2009
|
| Senior Scientist-Transfection Specialist |
| Demonstarted broad technical expertise in the area of mammalian cell transfections, both for soluble as well as cell bound protiens.
High level of technical expertise in tissue culture
Ability to design and execute plans, interpret results and summarize findings in the area transfection for optimal protein expression for immunization and screening
Prepare and be accountable for timelines
Ability to work well independently as well as part of mutidisciplinary teams
Strong communication skills
MS or PhD preferred with 8-12 years experience (excluding school)
A significant portion of the work for this position is at the bench.
|
| Strategic Diagnostics Inc. |
Newark |
DE |
11/20/2009
|
| Field Application Scientist |
| Credentials Required:
· Ph.D level scientist in Molecular Biology, Immunology or related sciences
· At least 5 years of experience generating of monoclonal and polyclonal antibodies, and/or production of antibodies in vitro and in vivo (ascites) and maintaining cell lines.
· Scientist/consultant with industrial expertise in research & development related to hybridoma technology and/or immunoassay development.
· Proficient or general understanding of Antibody Methodology (mono/polyclonal) such as:
-Rabbit, mouse, hamster or rat handling techniques;
-Mouse ascites fluid and/or hollow fiber bioreactor production of monoclonal antibodies;
-Lymphocyte cell fusions,
-Tissue culture and media formulations,
-Cell freezing techniques,
-Hybridoma fermentation and antibody purification;
-ELISA, RIA, IFA, Western Blot Analysis. MesoScale Platform, IHC techniques; Flow Cytometry (FACS)
-Cell transfections and Protein expression experiments
· Experience and high degree of comfort doing technical presentations
· Energetic, resourceful and highly motivated. Ability to think strategically and work independently.
· Ideally has commercial acumen and understand sales process. |
| Strategic Diagnostics Inc. |
Newark |
DE |
11/20/2009
|
| Manufacturing Manager |
|
--------------------------------------------------------------------------------
Manufacturing Manager
Location: Newark-Pencader
Job Code: 51
# of openings: 1
--------------------------------------------------------------------------------
Description
The Manufacturing Manager is responsible for planning, organizing, staffing directing and controlling production. The manager sets priorities, coordinates the scientists and operators work schedules to meet production requirements while maintaining a high quality standard. Leads continuous improvement programs to increase yield and reduce variation. Helps lead technical troubleshooting and root cause analysis efforts to reduce cost and improve output quality. The manager is an integral part of internal product/process redesigns, new product transfers from R&D and the integration and process transfer of external product/process acquisitions.
Responsibilities and Duties:
1. Manages and coordinates the Scientist/Operator production activities and schedules. Meets job schedules with acceptable quality.
2. Hires new employees and is responsible for operator training & certification, establishes standards of performance, conducts employee performance appraisals and on going coaching. Conducts corrective actions when disciplinary action is required and enforces company policies, rules and regulations.
3. Must be able to achieve completion of objectives through mentoring and coaching others..onitors and measures the department performance, strives for continual improvements in productivity and ways to increase capacity and reduce cost.
4. Monitors and measures the department performance, strives for continual improvements in efficiencies and reductions in variation and costs.
5. Takes ownership for the quality of products produced and services performed.
6. Is dedicated to reducing process variation and champions the use of statistical process control (SPC) and formal problem solving tools across all operations, trains employees in quality theory and practice, writes and modifies procedures to confirm to quality standards and maintains proficiency in problem solving techniques.
7. Responsible for the managing and replenishment of key custome reagents.
8. Responsible for the accuracy of the MRP system data, Bill of Material and Routings, Syspro standards and the material and labor variances.
9. Determines manufacturing capital and tooling needs. Is knowledgeable of the process specifications in his/her area of responsibility and is dedicated to the reduce process variation.
10. Continually works towards control of key equipment variables and process parameters associated with the lyophilizers, fermenters, centrifuges, balances, coating machines, reel-to-reel sprayer and dippers. Ensures equipment maintenance is appropriate and monitored.
11. Writes and follows standard operating procedures and makes certain paperwork is properly filled out and data collection systems reflect accurate product movements.
12. Is knowledgeable of the process specifications in the area of responsibility.
13. Makes sure process changes are documented before a new process or change is implemented on the production floor.
14. Communicates effectively with the Supply Chain Manager and Sales & Marketing to resolve customer performance problems, participates in customer audits and visits.
15. Complies with and aids in the development of department safety rules, monitors area for hazards, uses proper personal protective equipment (PPE) when required and maintains a safe, clean and organized work area.16. Monitors and maintains supplies, spare/contingency parts and WIP minimums to reduce downtime.
16. Performs other duties as assigned.
Qualifications :
BS/BA in biochemisty/microbiology/engineering field
At least 5 years of management experience in a manufacturing enviornment
Familiar with antibody and or immunoassays processes
Good mechanical and mathematical abilities and the ability to make critical judgments within the production processes.
Familiarity with antibody and/or immunoassay processes.
Computer proficiency- Word, Excel, PowerPoint, and Project expertise is preferred.
Knowledgeable of SPC and the use of data driven problem solving tools.
Good verbal and written communication skills.
Abilities:
Consistently meets production schedule deadlines
Consistently sets and meets production goals
Identifies and resolves production issues.
Establishes and makes changes to process for continuous improvement
Trains staff on process
Excellent organizational skills
Must be able to mutli-task
Must be able to apply priority management skills and assess the risk/benefits of decisions and actions.
Supervisory Responsibilities:
Manages a staff of technical and labor personnel. Responsibilities include interviewing, hiring and training new employees, planning, assigning and directing work, conducts employee appraisals, on-going coaching sessions provides a motivating work environment, enforces company policies, rules and regulations and maintains cooperation with other areas.
Work Environment/ Other requirements:
At SDI our work environment varies significantly from job to job. Ability to lift or move 20 pounds and work/travel throughout plant environment of varied temperatures and humidity; grasp and hold small objects, a full range of motion, and to wear personal protective devices. This position may expose the employee to fumes or airborne particles, biohazards, and toxic or caustic chemicals. Daily contact with employees in other departments is required.
|
| Strategic Diagnostics Inc. |
Newark |
DE |
11/20/2009
|
| Senior Scientist-Process Engineer |
| Experience in lateral flow, immunoassay, bioluminescence and other bioassays is preferred. MS or PhD generally required for this level with 8-12 years of experience. Individual must demonstrated technical expertise in a related business or field. Must be familiar with accepted industry practices and regulations. Prefer experience in a Food Industry, or Biopharmaceutical/Pharmaceutical Manufacturing environment. |
| Strategic Diagnostics Inc. |
Newark |
DE |
11/19/2009
|
| Scientist III |
| Qualifications: (Knowledge, Skills and Abilities: Education, Experience, Job Skills, Equipment Skills, and Certifications)
1. B.S/B.A. in Biology, molecular biology, Chemistry, biochemistry/ microbiology/ immunology/ medical technology field with 5+years. MS or PhD generally required for this level with 1-2 years of experience.
2. Strong knowledge of QSR, cGMP and ISO regulations and guideline
3. Fully knowledgeable of Instrumentation used in molecular biology.
4. Demonstrated skill in the areas of protein purification and analysis; such as IMAC, Gel filtration, western blot.
5. Demonstrated skill in the areas of DNA manipulation; such as PCR and gene construction, sub-cloning and sequence analysis.
Supervisory Responsibilities:
May manage a team of scientists and technicians performing, training, coaching and aid in quarterly and yearly performance reviews, conducts disciplinary discussions as appropriate.
Abilities:
1. Thorough understanding of molecular biology and protein biochemistry.
2. Must be familiar with accepted industry practices and regulations
3. Maintain broad knowledge of current scientific theories and practices.
4. Able to multitask
5. Able to work independently and lead a team of scientists
6. Able to organize and prioritize tasks for his/her self and others
7. Able to resolve problems with others
8. Good verbal and written communication
9. Develops SOP’s
10. Documents coaching
Work Environment / Other Requirements:
Works in a variety of lab environments that could lead to exposure to heat, cold, dry air, chemicals, odors and humidity. Ability to lift 50 pounds required
|
| Morphotek®, Inc. |
Exton |
PA |
11/19/2009
|
| Associate Director, Aseptic Fill Finish Operations |
| Knowledge/Skills/Abilities Required
Strong knowledge of aseptic manufacturing of biologics as well as ICH, cGMP, EMEA and JP guidelines as they pertain to the manufacturing of monoclonal antibody based therapies required.
Minimum 8 years of relevant aseptic manufacturing experience with biologics, several of which must be in a management position required. Graduate level degree in biological sciences or related subject highly preferred. Individuals without a graduate degree but more experience will be considered.
Prior contract manufacturing project management experience is highly preferred. Prior experience with manufacturing from pre-IND through phase 3 or commercial production is highly desired.
An understanding of project accounting and financial concepts required.
A hands-on, proactive stance is essential with willingness and ability to assist all team members to achieve corporate goals required.
Up to 20% domestic and international travel required. |
| Morphotek®, Inc. |
Exton |
PA |
11/19/2009
|
| Training Administrator |
| Knowledge/Skills/Abilities Required
BA/BS in Business Administration, Human Resources, or a related field required.
2-3 years training, career counseling, career development or related experience in the biotechnology or pharmaceutical industry required.
Previous experience designing, delivering and/or implementing training programs required.
Experience in Learning Management Systems (LMS) and solid understanding of training operations required.
Advanced proficiency in MS Office applications required.
Excellent organizational, written communication, verbal communication, facilitation, presentation and interpersonal skills required.
Proven ability to work independently required.
Occasional travel may be required. |
| Morphotek®, Inc. |
Exton |
PA |
11/19/2009
|
| Director, Analytical Outsourcing Program Management |
| Graduate level degree in biological sciences or related subject required. Ph.D. highly preferred with equivalent expertise required.
Must have a minimum of 8 years of relevant analytical experience with biologics, several of which must be in a management position.
Strong knowledge of biologics manufacturing and analytical methodology as well as ICH, cGMP, EMEA and JP guidelines as they pertain to the manufacturing of monoclonal antibody based therapies required.
Prior contract manufacturing project management experience is highly preferred. Prior experience with manufacturing from pre-IND through phase 3 or commercial production is highly desired.
An understanding of project accounting and financial concepts is also required since this individual will participate in budgeting, tracking and financial decision making for multiple drug development programs.
A hands-on, proactive stance is essential with willingness and ability to assist all team members to achieve corporate goals.
Excellent interpersonal skills are mandatory, in addition to analytical problem solving, the ability to set priorities and achieve goals; strategic thinking, energy, enthusiasm and an entrepreneurial mindset.
The ability and willingness to travel (domestic and international) approximately 20% of the time is required. |
| Radiometer America, Inc. |
Northern California |
CA |
11/19/2009
|
| Sales Representative |
| •Bachelor’s degree in respiratory, biology, or chemistry preferred.
•2 to 5 years in medical capital equipment sales experience with proven accomplishments clinical lab or similar work. Immunoassay experience required.
•Qualified candidate will have good organization, time management and presentation skills.
•Ability to communicate at all levels internally and externally with customers.
•Extensive travel – 50%+
If you are unable to apply electronically because of a disability, dial 711 to apply through the Ohio Relay and ask to be connected to the Human Resources Department at 440-871-8900.
Radiometer America Inc. is an equal opportunity / affirmative action employer and does not discriminate on the basis of race, color, gender, national origin, ancestry, religion, martial status, age, veteran status or disability or any other legally protected characteristics that may vary by state, city and/or county of employment.
|
| Radiometer America, Inc. |
Dallas or Houston |
TX |
11/19/2009
|
| Transcutaneous Sales Specialist |
| •Bachelor’s degree in Science (i.e. Biology, Chemistry) or Nursing
•3+ years clinical experience in Respiratory Care, Hyperbaric/Wound Care Medicine or Cardiology
•3+ years medical capital sales experience
•Strong organizational, time management, territory planning skills
•Dynamic, high-energy individual to implement sales activities
•50% travel
If you are unable to apply electronically because of a disability, dial 711 to apply through the Ohio Relay and ask to be connected to the Human Resources Department at 440-871-8900.
Radiometer America Inc. is an equal opportunity / affirmative action employer and does not discriminate on the basis of race, color, gender, national origin, ancestry, religion, martial status, age, veteran status or disability or any other legally protected characteristics that may vary by state, city and/or county of employment.
|
| Radiometer America, Inc. |
Quebec |
C09 |
11/19/2009
|
| Sales Representative |
| •Bachelor’s degree in respiratory, biology, or chemistry preferred.
•2 to 5 years in medical capital equipment sales experience with proven accomplishments clinical lab or similar work. Immunoassay experience required.
•Qualified candidate will have good organization, time management and presentation skills.
•Ability to communicate at all levels internally and externally with customers.
•Extensive travel – 50%+
|
| CommonHealth |
Parsippany |
NJ |
11/20/2009
|
| Medical Strategist |
| Knowledge and Skills
MD
Ideally internal medicine background with broad range of experience, especially in oncology and neuropsychiatry
Ideally, agency, med-ed and/or pharma industry experience
CommonHealth is an equal opportunity employer
|
| CommonHealth |
Parsippany |
NJ |
11/20/2009
|
| Medical Writer |
| Knowledge and Skills
Doctoral level education in biomedical sciences preferrably (PhD, PharmD, MD) oncology experience required
Knowledge of assigned therapeutic areas
Experience writing peer-reviewed articles, distilling complex technical information for a variety of medical audiences
Familiarity with RefMan or similar database program, Word, PowerPoint
Familiarity with AMA style writing
Ability to write high-quality scientific articles
Demonstrated written and verbal communications skills
Ability to work as a team member
Problem Solving
Balancing work quality with timelines
Adopting the writing style to the target audience
Managerial Direction
Make decisions regarding content and style in consultation with program management and account management
Self management to adhere to agreed T&E schedules, budgets, and to alert team to potential deviations and overages
We are an equal opportunity employer
|
| CommonHealth |
Parsippany |
NJ |
11/20/2009
|
| Medical Director |
| Requirements:
2+ years experience in patient care or medical education
Advanced degree in biomedical sciences (PharmD, PhD, MD)
Developing educational concepts and content through critical analysis of data, distilling complex technical information for a variety of medical audiences, working with opinion leaders
Knowledge of CME procedures
Writing proposals
Editing documents
Clinical research and publication experience is a plus.
Ability to provide independent medical direction
Strong written and verbal communication and presentation skills.
Software: Microsoft Word, PowerPoint, reference database programs such as Refman
Familiarity or interest in pharmaceutical marketing
Must work well in a team-oriented environment
Ability to meet deadlines while working on multiple, parallel projects
Develop solid understanding of the market and goals advocated by the medical and marketing clients
We are an equal opportunity employer.
|
| Boston Scientific |
Valencia |
CA |
11/19/2009
|
| Marketing Manager |
| Experience:
· Prefer minimum of 3 years experience in a medical-related industry in a product management, sales or marketing position with product launch experience.
· Field medical sales, technical and/or marketing communications experiences a plus.
SPECIALIZED KNOWLEDGE & SKILLS:
· Must have excellent communication skills, including the ability to listen to clinical and customer needs, prioritize needs/requirements and communicate them to cross-functional teams, including physicians.
· Must have exceptional leadership, presentation, negotiation and interpersonal skills, particularly in working effectively as a member of a team.
· Must be able to work in a fast paced environment and foster constructive relationships with internal and external customers.
· Must have excellent and professional written and verbal skills.
· Must have excellent analytical skills.
· Must have good presentation skills.
EDUCATION and TRAINING:
· Bachelor’s degree
· MBA preferred
PHYSICAL ENVIRONMENT / WORKING CONDITIONS:
· Must have the ability to handle the stresses of 25% or more travel schedule. Ability to independently manage a moderate travel schedule. Ability to be flexible in working extended schedules, including some weekends.
RESPONSIBILITY FOR PERSONNEL:
Direct Supervision: None
Indirect Supervision: None
INTERNAL CONTACTS: All levels of Sales, Engineering, Management staff, department heads, Marketing, Purchasing, Finance, Human Resources, QA, Regulatory and Clinical staff.
EXTERNAL CONTACTS:
Vendors: Vendors for all types of marketing services used in the development and promotion of medical devices; specifically, advertising agencies, market research firms, sales training organizations, graphics developers, etc.
Consultants: Scientific and health care industry consultants.
Customers: Clinicians (Referring Physicians, Implanting Physicians, Allied Health Care Providers), Hospitals and Hospital Systems, Patients, Payer Organizations, etc.
Other: University Professors and Research groups working in the Bioengineering field and the Implantable Device field.
Boston Scientific is an Equal Opportunity Employer, EEO/AA
|
| Sysmex |
Mundelein |
IL |
11/19/2009
|
| Manager, Technical Assistance Manager |
| 4- Year Bachelor's Degree in Medical Technology or Biomedical Engineering - Operations management experience and direct or indirect experience working in the clinical laboratory environment. Call Center experience helpful, technical troubleshooting with medical diagnostic equipment a plus. Demonstrated analytical and technical skills used in strategic planning and forecasting using MS Excel/database knowledge. The successful candidate must be able to communicate effectively with all levels in the organization. Strong project and team management skills required.
We are proud to be an EEO/AA employer M/F/D/V. We maintain a drug-free workplace and perform pre-employment substance abuse testing. |
| openQ |
Charlottesville |
VA |
11/19/2009
|
| Data Research Project Manager |
| Skills:
• Very thorough understanding of life sciences industry
• Understanding of, and comfort with, reading medical literature and performing information searches on medically-related topics
• Excellent verbal and written communication skills
• Strong analytical skills and technical understanding of data acquisition, data structuring and data quality control
• Prior experience interfacing with customers about data-related projects
• Strong team player and the proven ability to work independently
Education:
• PhD in life sciences field preferred or Master’s degree and preferably at least 5 years relevant experience in life sciences driven data company
|
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| WW Senior Strategic Marketing Manager |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| WW Controller Cell Analysis |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| VP Manufacturing Injection |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| VP Manufacturing Infusion |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Validation Technician II |
| See above |
| BD (Becton, Dickinson and Company) |
Burlington |
NC |
11/20/2009
|
| Validation Engineer I |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Validation Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Technical Writer IV |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Technical Team Member- ADVANCED MOLDING SKILLS |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Technical Team Member |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Technical Team Member |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Technical Team Member |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Technical Team Member |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Technical Team Member |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Technical Support: Technical and Informatics Support Specialists (TAISS) |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Technical Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Technical Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Technical Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Technical Associate |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Technical Applications Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Tech Transfer Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Team Leader, Customer Service |
| See above |
| BD (Becton, Dickinson and Company) |
Holdrege |
NE |
11/20/2009
|
| Team Leader |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| System Project Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Support Technician |
| See above |
| BD (Becton, Dickinson and Company) |
Bedford |
MA |
11/20/2009
|
| Supply Network Planner |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus |
NE |
11/20/2009
|
| Summer Engineering Internship |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Strategic Sourcing Manager - Professional Services & Manufacturing |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Strategic Sourcing Manager - Indirect Services |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Strategic Sourcing Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Strategic Sourcing Analyst |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Strategic Marketing Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Strategic Innovation Leader |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Staff Engineer, Packaging Technology |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Staff Engineer - Environmental Sustainability |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Sr. Systems Analyst - Logistics Execution |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Sr. Product Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Sr. Packaging Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Sr. Manufacturing Equipment Engineer - Reagents |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Sr. Financial Analyst - Finance Leadership Development Program (2 of 2) |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Sr. Electro-Mechanic |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Sr. Cost Analyst |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Sr Scientist |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Sr Reagent Dev Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Sr Brand Manager, Hospital & Insitutional |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Sr Algorithm Scientist Developer |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Software Project Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Software Project Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Research Triangle Park |
NC |
11/20/2009
|
| Software Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Holdrege |
NE |
11/20/2009
|
| Six Sigma Coordinator |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Service Assurance Representative |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Senior Scientist |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Senior Regulatory Affairs Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Senior Quality Engineer, Pen Injection Platform |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Senior Project Engineer - Molding |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Senior Project Engineer - Assembly |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Senior Product Manager - Vaccines |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Senior Paralegal - Procurement Contracts |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Senior Marketing Manager, Strategic Marketing |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Senior Marketing Manager ? Multiplexed Assay Products |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Senior Intellectual Property Counsel |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Senior Engineer, Quality Systems |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Senior Engineer, Packaging Technology, BD Medical Surgical Systems |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Senior Clinical Trial Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Senior Clinical Research Associate (IVD strongly preferred) |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
11/20/2009
|
| Scientist II - Molecular Biology |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
11/20/2009
|
| Scientist I |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
11/20/2009
|
| Scientist I |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Scientist I |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Scientist |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Scientific Affairs Liaison |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
11/20/2009
|
| Research Associate III |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Research Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Mebane |
NC |
11/20/2009
|
| Research & Development Validation Engineer II |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Reliability Engineer II |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Regulatory Compliance Complaint Analyst |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Regulatory Affairs Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Regulatory Affairs Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Mebane |
NC |
11/20/2009
|
| Receiving Associate II |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Rebate Reconciliation Associate |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Reagent Dev Associate III |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Reagent Dev Associate III |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| R&D Sr. Optical Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| R&D Mechanical Project Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| R&D Manager, Technology Development |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| R&D Manager, Packaging Technology |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| R&D Manager, Infusion Systems |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| R&D Manager, Emerging Markets |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| R&D Electrical Project Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| R&D Director, Preanalytical Systems |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| R&D Director, Additive and Chemistry |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Quality Systems Leader |
| See above |
| BD (Becton, Dickinson and Company) |
Burlington |
NC |
11/20/2009
|
| Quality Engineer II, Reagents |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Quality Engineer II |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Quality Engineer II |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Quality Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Quality Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Woburn |
MA |
11/20/2009
|
| Quality Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Quality Control Microbiologist |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| QA Technician II -FPR |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
11/20/2009
|
| QA Inspector I |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus |
NE |
11/20/2009
|
| PS Site IT Leader |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Project Manager, IT |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Project Engineer - Packaging |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Project Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Program Manager |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Production Technician II |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Production Technician I |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Production Supervisor |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Production Planner/Buyer |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Production Operator IV |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Production Operator III |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Production Operator III |
| See above |
| BD (Becton, Dickinson and Company) |
Waltham |
MA |
11/20/2009
|
| Production Operator II |
| See above |
| BD (Becton, Dickinson and Company) |
Waltham |
MA |
11/20/2009
|
| Production Operator I |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Production Mechanic |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Production Chemist I |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Product Manager, Scientific Services |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Product Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Product Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Product Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Process Technician/Mold Set Up -- Trainee |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Process Technician |
| See above |
| BD (Becton, Dickinson and Company) |
Canaan |
CT |
11/20/2009
|
| Process Engineer - Molding |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus |
NE |
11/20/2009
|
| Process Automation and Development Engineer - Cannula Operations |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Principal Scientist, Advanced Technology - Medical Surgical Systems |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Principal Engineer- R&D Platform |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Principal Engineer, Mechanical Engineer - Hypodermic team |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Principal Engineer, Environmental Packaging |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Principal Engineer - Technical Lead |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus |
NE |
11/20/2009
|
| PosiFlush Manufacturing Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Teterboro |
NJ |
11/20/2009
|
| Pilot/Aircraft Captain Corporate Flight Department |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| New Product Launch Coordinator |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus |
NE |
11/20/2009
|
| Moldmaker |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Molding Technology Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Microbiologist |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Metallurgist/Materials Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Medical Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Mechanical Engineer w/ FEA, Medical Surgical Systems |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Mechanical Engineer / Senior Mechanical Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Mechanical Design Engineer, Medical Surgical Systems |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Master Data Coordinator |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
11/20/2009
|
| Marketing Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Manufacturing Technician II (Packaging) |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Manufacturing Technician I |
| See above |
| BD (Becton, Dickinson and Company) |
Waltham |
MA |
11/20/2009
|
| Manufacturing Technician - Production |
| See above |
| BD (Becton, Dickinson and Company) |
Woburn |
MA |
11/20/2009
|
| Manufacturing Supervisor |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
11/20/2009
|
| Manufacturing Manager - Tissue Culture |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Manufacturing Integrator, Diabetes Care |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Manufacturing Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Manufacturing Associate I |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Manager, Corporate Communications |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Manager US Regulatory Affairs |
| See above |
| BD (Becton, Dickinson and Company) |
Burlington |
NC |
11/20/2009
|
| Manager Technical Product Support Cervical Programs |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Manager International Regulatory Affairs |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Maintenance Technician III-IV |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus |
NE |
11/20/2009
|
| Luer Forming Set-Up Operator B Shift |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus |
NE |
11/20/2009
|
| Luer Forming Set-Up Operator A Shift |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Lead Technical Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Lead Technical Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Lead Business Unit Coordinator |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Laboratory Technician |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Internal Audit Director |
| See above |
| BD (Becton, Dickinson and Company) |
Broken Bow |
NE |
11/20/2009
|
| Intern -Engineering Process/Electrical |
| See above |
| BD (Becton, Dickinson and Company) |
Broken Bow |
NE |
11/20/2009
|
| Intern - Quality Engineer/Microbiology |
| See above |
| BD (Becton, Dickinson and Company) |
Broken Bow |
NE |
11/20/2009
|
| Intern - Information Technology (IT) |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
11/20/2009
|
| Instrumentation Technician I |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Instrument Assembly Associate I |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Inspection Technician II |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Information Technology Senior Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Immunoassay Development Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
11/20/2009
|
| Human Resources Administrative Assistant |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| HR Business Strategy Leader |
| See above |
| BD (Becton, Dickinson and Company) |
Research Triangle Park |
NC |
11/20/2009
|
| Global Business Systems Analyst -Manufacturing Execution System Implementation |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Finance Manager - WWIT |
| See above |
| BD (Becton, Dickinson and Company) |
Kansas City |
MO |
11/20/2009
|
| Field Sales Consultant - Acute Care - Kansas City |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Facilities Maintenance Technician I |
| See above |
| BD (Becton, Dickinson and Company) |
Holdrege |
NE |
11/20/2009
|
| Facilities Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Engineering Technician |
| See above |
| BD (Becton, Dickinson and Company) |
Research Triangle Park |
NC |
11/20/2009
|
| Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus |
NE |
11/20/2009
|
| Electromechanical Technician 1st shift |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| EBusiness Applications Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| E-Business Analyst |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Distribution Manager |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Director of Campaigns |
| See above |
| BD (Becton, Dickinson and Company) |
Mebane |
NC |
11/20/2009
|
| Diagnostic Instrument Value Stream Lead |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Customer Service Representative |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Customer Service Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Cost Accounting Supervisor |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus |
NE |
11/20/2009
|
| Cost Accountant |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Core Team Leader- R&D Platform |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Core Team Leader- R&D Platform |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Core Team Leader |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Core Team Leader |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Commercial Development Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Clinical Project Lead |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Clinical Data Management Group Leader |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Clinical Data Analyst |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Calibration Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus |
NE |
11/20/2009
|
| Business Analyst |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Bioprocess Engineer II |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Bioprocess Engineer II |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Bioprocess Engineer I |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Bioprocess Engineer I |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Bioprocess Engineer I |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| BioPharma Market Development Manager |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
11/20/2009
|
| Biochemist I |
| See above |
| BD (Becton, Dickinson and Company) |
Woburn |
MA |
11/20/2009
|
| Bioanalytical Chemist |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Automation Technician II |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Administrative Assistant |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Accounts Receivable Associate |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Accounting Manager |
| See above |
| Agilent Technologies, Inc. US |
Westlake Village |
CA |
11/20/2009
|
| Field Service Engineer- Westlake Village |
| Description : Representative for the Life Sciences and Chemical Analysis Group (LSCA) of Agilent Technologies. Responsibilities include on-site installation, customer training, repair and troubleshooting of hardware, and provide routine preventative maintenance, qualifications, and verification services. Typical products include Liquid Chromatographs, Gas Chromatographs, Mass Spectrometers, UV/VIS Spectrophotometers and Data Systems. Job focus will be on customer satisfaction by providing customers with high quality services. Other responsibilities include adherence to environmental health and safety guidelines, managing parts, coordinating resources, training, organization, providing feedback to manufacturing divisions, working with sales forces, and maintaining up to date technical knowledge for assigned products. Will be part of a team that delivers on-site services at a major account.
Agilent Technologies is the world's premier measurement company. Agilent provides core electronic and bio-analytical measurement tools to engineers, service providers, researchers and scientists in the electronics, communications, life science research, environmental and petrochemical industries.
~cb~11/17/09 |
| Agilent Technologies, Inc. US |
Loveland |
CO |
11/20/2009
|
| R&D Software Intern |
| Qualifications:
Completion of junior year at an accredited 4- year university working toward a degree in Electrical Engineering, Computer Engineering or Computer Science.
? Working knowledge of C++.
? Knowledge of objected oriented programming concepts and design.
? The ability to work in a team and across geographic boundaries.
? Good verbal and written communication skills.
cb~11/14/2009 |
| Agilent Technologies, Inc. US |
Santa Rosa |
CA |
11/20/2009
|
| Productivity Engineer |
| Musts
- 5 years minimum experience in PCB layout
- 3 years minimum experience in high-speed digital and/or high-frequency RF PCB layout
- Expertise with Mentor Graphics Expedition and specifically Expedition CES
- Expertise in manufacturing output processes, data, and tools
- Experience with Mentor BoardStation layout
- Excellent troubleshooting skills and ability to trace problems to root cause in layout
- Knowledge and familiarity with PCB fabrication and assembly technologies and processes
- Experience with the Valor design rule checker
- AS degree in electronics, Computer-Aided drafting, or equivalent
- Excellent communication skills and ability to do multitasking
- Good computer skills
Wants
Skill or experience in the following areas would be a plus, but aren't required.
- Programming skills in scripting (e.g., VBscript, Perl, Javascript)
- Documentation and technical writing skills
- Familiarity with component library and schematic tools
- Electronic circuit design experience
- Familiarity with other PCB tools besides Mentor Graphics (e.g., Cadence, Zuken, Intercept) and can objectively evaluate and recommend best tools and practices
- Experience in systems and EDA tool administration
- Bachelors degree in electrical engineering or equivalent
~cb~11/17/09 |
| Agilent Technologies, Inc. US |
San Diego |
CA |
11/20/2009
|
| Field Service Technician |
| Qualifications: Associates Degree in Electronics or recent Military experience/training in electronic measurement calibration and a minimum of 2 years field experience.
Position requires:
? Hands-on Experience as Field Service Engineer or Maintenance Technician
? Knowledge of the calibration and repair of all types of electronic equipment
? Excellent communication skills (customer interface skills)
? Strong organizational skills
? Positive/Energetic attitude
? Willingness to learn |
| Agilent Technologies, Inc. US |
El Segundo |
CA |
11/20/2009
|
| RF and Microwave Field Applications Engineer |
| Position requires Bachelors or Master Degree or equivalent and a minimum of 1-2yrs relevant experience with typically 2-4yrs in an Applications Engineering or Sales support role.
? 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
? Must be US Citizen
~cb~11/13/09 |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
11/20/2009
|
| Engagement Manager |
| Qualifications:
? Bachelors Degree or equivalent plus a minimum of 10 years relevant experience in IP networks especially routing, switching and various tunneling protocols
? A strong technical background in communications and computer technologies is required
? Previous marketing and/or sales experience is required
? Proven management experience is required
? A demonstrated ability to work with sales teams, senior management and directly with customers is required
? Strong communications skills both written and verbal are required
Preferences:
? Some form of network certification (i.e., CCNA, JNCIS, etc.)
? MBA or advanced degree
? Experience with voice and video IP based communication
? Wireless network experience
? Enterprise and/or Service Provider experience
? Experience in network management, monitoring and troubleshooting
~cb~8/29/2009 |
| Agilent Technologies, Inc. US |
Cedar Creek |
TX |
11/20/2009
|
| Manufacturing Associate-Intermediate |
| This position requires a BS/BA degree in biological science or related field and one (1) to two (2) years of previous experience in chemistry, molecular biology and/or biochemistry. A strong working knowledge of standard laboratory techniques of molecular biology is required ( PCR, DNA and RNA isolation, bacterial transformations). Strong oral and written communication, organization, team building and computer skills essential.
cb~11/11/2009 |
| Agilent Technologies, Inc. US |
Columbia |
MD |
11/20/2009
|
| Federal Inside Account Manager |
| ? The successful candidate needs to have at a minimum a BS Degree in the science such as Chemistry, Biology, Biochemistry or Physics.
? The ability to identify legislative funding to key agencies is necessary. Collaborating with Agilent's Government Affairs Office is required to facilitate earmark funding opportunities.
? Computer web searching and conducting federal business research and familiarity with the federal government's E-Buy and FedBizOpps and miscellaneous electronic interfaces is a requirement.
? They should have a strong understanding and can demonstrate computer skills and utilize programs to include Microsoft Office Suite 2007, Visio, Adobe etc.
? Excellent organization, written and verbal communication skills are required. Exception telephone communication skills are required and should be able to be demonstrated.
? The ability to research, formulate , format and organize electronic information to include sales data, government agency budget information, regulatory guidance affecting the federal programs, should be demonstrated and is required.
? Excellent probing and questioning skills required.
? A fundamental understanding of the sales process from prospecting and cold calling through closing deals is desired.
? The ability to use Customer Relationship Management software is desired. Previous experience with SAP-CRM is desired.
? The ability to accurately predict and forecast business close dates is desired.
? The ability to negotiate and mitigate critical customer issues is desired.
? The ability to configure and quote Agilent systems for sale is desired. |
| Agilent Technologies, Inc. US |
Garden Grove |
CA |
11/20/2009
|
| Scientist I |
| MS/Ph.D. or equivalent industrial experience required
Strong protein chemistry background essential:
- conjugation
- purification
Experience working with immunoglobulins desired
Diagnostics industry experience desired
~cb~11/11/09 |
| Agilent Technologies, Inc. US |
Cedar Creek |
TX |
11/20/2009
|
| Distribution Associate I |
| ? High school diploma or general education degree (GED); or zero (0) to three (3) years related experiences and/training; or equivalent combination of education and experience.
? Ability to demonstrate an understanding at a level that may include addition, subtraction, multiplication and division in all units of measure using whole numbers, common fractions and decimals.
? Ability to read and interpret at a level that may include documents such as safety rules, operating instructions and procedural manuals.
? Ability to apply common sense understanding to carry out instructions furnished in written, oral or diagram form. Requires basic computer operations skills. Awareness and or ability to use Microsoft Office Suite tools.
Certification:
? Forklift Operator Certification, required within 90 days.
Other skills:
? Knowledge of commonly used practices and procedures within distribution and warehousing.
Physical demands:
? The physical demands described here are representative of those demands that must be met by the employee to successfully perform the essential functions of the 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, reach with hand and arms, sit, climb, balance or stoop, kneel, crouch or crawl, regularly lift and/or move up to 15 pounds and occasionally lift and/or move up to 100 pounds. Specific vision abilities required include accurate close vision, distance vision and depth perception.
Work Environment:
? The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of the job. While performing the duties of this job, the employee is frequently exposed to extreme cold and loud noises. the employee is occasionally exposed to moving mechanical parts, high, precarious places and toxic or caustic chemicals requiring steel toed shoes to be worn at all times and occasionally hard hats. |
| Agilent Technologies, Inc. US |
La JollaSanta Rosa |
CA |
11/20/2009
|
| MEMS Intern |
| You will have completed a Master's Degree and will be pursuing a Ph.D. |
| Agilent Technologies, Inc. US |
Roseville |
CA |
11/20/2009
|
| Service Tech Coordinator - Career |
| Position requires:
? Electronics degree, Military Certificate, or equivalent experience required.
? Experience in the electronic instrumentation repair/calibration industry
? Ability to work with minimal supervision and interface effectively with fellow team members, customers and management
? 1+ years direct experience in calibration, diagnosis, troubleshooting and repair to the assembly/component level of Agilent Spectrum Analyzers is highly desired
? Strong abilities in use of technical manuals and schematics
? Competent Computer skills
? Knowledge of Total Quality Methodologies
? Direct experience on Agilent instrumentation and automated calibration systems is preferred
? PMEL/Metrology background is a plus
Geo Location: Roseville, CA
~cb~11/06/09 |
| Agilent Technologies, Inc. US |
Fishkill |
NY |
11/20/2009
|
| Field Service Technical Engineer--Account Management- NJ |
| Description : As the Field Service Engineer for a high tech growth business serving the Life Sciences markets, your primary responsibilities will include: account management, as well as, providing support on analytical LC, GC and MS products for customers, on-site. This role will provide you with the opportunity to join the Life Sciences and Chemical Analysis Group (LSCA) of Agilent Technologies.
Agilent Field Service Engineers deliver technical expertise to customers based on Agilent products and services primarily in the MS area. As an individual contributor, this job will focus primarily on large account management by providing customers with high quality services to ensure customer satisfaction. Responsibilities include on-site installation, customer training, repair and troubleshooting of hardware, and provide routine preventative maintenance, qualifications, and validation services. Other responsibilities include, adherence to environmental health and safety guidelines, understanding our customers business, parts management, coordinating resources, training, organization, providing feedback to manufacturing divisions, working with sales forces, and maintaining up to date technical knowledge for assigned products. We are looking for enthusiastic individuals who want to grow with our company and become part of a dedicated group of individuals.
~cb~11/05/09 |
| Agilent Technologies, Inc. US |
Westlake Village |
CA |
11/20/2009
|
| Field Service Engineer- Westlake Village |
| Description : As the Field Technical Support Representative for a high tech growth business serving the Chemical Analysis and Life Science markets, your primary responsibilities will include: Installation, repair and qualification services for Agilent and non-Agilent analytical instruments (LC/GC/MS) products for customers, on-site. Provides service in accordance to a maintenance contract, which may involve a managed service arrangement. Will be part of a team that delivers services on-site for large volume customers.
Perform the duties of a Customer Service Representative for the Life Sciences and Chemical Analysis Group (LSCA) of Agilent Technologies. Responsibilities include on-site installation, customer training, repair and troubleshooting of hardware, and provide routine preventative maintenance, qualifications, and verification services. Typical products include Liquid Chromatographs, Gas Chromatographs, Mass Spectrometers, UV/VIS Spectrophotometers and Data Systems. Job focus will be on customer satisfaction by providing customers with high quality services. Other responsibilities include adherence to environmental health and safety guidelines, managing parts, coordinating resources, training, organization, providing feedback to manufacturing divisions, working with sales forces, and maintaining up to date technical knowledge for assigned products.
Agilent Technologies is the world's premier measurement company. Agilent provides core electronic and bio-analytical measurement tools to engineers, service providers, researchers and scientists in the electronics, communications, life science research, environmental and petrochemical industries.
~cb~11/05/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| Applications Engineer |
| Requires:
- BS in biology, biochemistry, molecular biology; related discipline or equivalent. Master or PhD preferred.
- 3+ years experience with life science software products
- Experience with systems biology software products
- Experience in interacting with customers in a pre-sales and/or post sales support role
- Experience in generating and presenting technical training materials
- Experience in interacting with cross-functional groups including sales, marketing and R&D
Geo Location: Santa Clara, California |
| Agilent Technologies, Inc. US |
Garden Grove |
CA |
11/20/2009
|
| Marketing Manager |
| -Educated to at least university degree level years10 years' practical experience, including 5+ years' experience managing sales and marketing in Clinical Diagnostics. Here's where your people skills, technical knowledge and influential leadership ability will really make an impact.
~cb~11/05/09 |
| Agilent Technologies, Inc. US |
Wilmington |
DE |
11/20/2009
|
| Customer Account Specialist |
| ? Bachelor of Arts or Bachelor of Science degree
? Ability to travel
? Relevant customer experience
Geo Location: Wilmington, DE
~cb~11/11/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| HPLC Bio-Separations Application Chemist |
| ? Advanced Degree in Biochemistry, Molecular and Cellular Biology, or equivalent (demonstrated by 5+ years working experience in analytical HPLC bio-separations and confirmation of technical HPLC and Bio-Chromatography knowledge)
? Demonstrated expertise in operating HPLC systems and using a variety HPLC Bio-Columns including ion exchange, size exclusion, reverse phase, hydrophobic interaction and affinity
? Demonstrated experience in operating LC/MS and/or capillary electrophoresis systems for Biologic analysis preferred but not required
? Proven track record of self motivation and initiative
? Excellent verbal and written communication skills
? Ability to travel world wide as required up to 30% of the time
? Biopharmaceutical or Biotechnology expertise is critical to this position
~cb~11/01/09 |
| Agilent Technologies, Inc. US |
Columbia |
MD |
11/20/2009
|
| System Engineering Specialist |
| Qualifications:
?Bachelors or Master Degree or University 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 UMTS, GPRS, GSM and CDMA technologies and Central Office networking.
?Experience with Perl and Shell Scripting as well as administration of Operating Systems: Linux and UNIX.
?Experience with end user, installation and commissioning of new systems within customer environments is highly desired.
?Strong interpersonal/relationship skills, solid written and verbal communications.
?US citizenship required
?Current US Government Security Clearance -or- ability to process for and obtain US Government Security Clearance.
Position will be located in northern Virginia or Maryland area. |
| Agilent Technologies, Inc. US |
Columbia |
MD |
11/20/2009
|
| Senior System Engineer |
| Qualifications:
?BS/MS in EE or Computer Science and 5+ years of demonstrated experience in architecting and implementing complex solutions for Telco and/or IP Networks.
?Experience in design and/or support using OSI model and current evolutionary trends in Telecoms and IP networks.
?Administration of Operating Systems: Linux and UNIX with working knowledge of Perl and Shell Scripting.
?A broad telecom background and IP technology expertise is essential including UMTS, GPRS, GSM and CDMA technologies and Central Office networking.
?Ability to develop written proposals and participate in the creation of RFI/RFP responses.
?Strong interpersonal/relationship skills with superior verbal and written communication to effectively communicate with the customer, executives and team-members.
?US citizenship required
?Current US Government Security Clearance -or- ability to process for and obtain US Government Security Clearance is also required.Position will be located in northern Virginia or Maryland area. |
| Agilent Technologies, Inc. US |
Columbia |
MD |
11/20/2009
|
| Signaling Analysis Application Specialist |
| Qualifications:
?Bachelors or Master Degree or University Degree in Electrical/Electronic or Computer Engineering and 5+ years applicable experience in architecting and implementing complex software solutions with a deep understanding of communication protocols (GSM/CDMA/GPRS/UMTS/VoIP/IP).
?Knowledge of Agilent products such as Signaling Analyzer, acceSS7 and or prior experience with telecommunications network monitoring platforms in wire line, cellular telecom, and IP is desired.
?Familiarity with the community?s architecture and interfaces is desired.
?Familiarity with OSI model and current/evolving telecoms standards with a strong background in IP.
?Experience with programming languages C/C++, Perl and Shell Scripting and administration of Operating Systems: Linux and UNIX.
?Strong interpersonal/relationship skills, solid written and verbal communications.
?US citizenship required
?Current US Government Security Clearance -or- ability to process for and obtain US Government Security Clearance is also required.
Position will be located in northern Virginia or Maryland area. |
| Agilent Technologies, Inc. US |
Columbia |
MD |
11/20/2009
|
| Operations Specialist |
| Qualifications:
?AA or BA in Business and 4-6 Years of equivalent Experience.
?Previous military logistics acquisition/supply chain or previous experience as a program administrator for a major systems integrator company is desirable.
?Extremely strong organizational skills and muti-tasking ability is required for support of multiple projects, customers and teams.
?Strong business process skills, including business analytical skills is required with the ability to work independently for business process creation and improvement.
?Solid team player with strong interpersonal/relationship skills with superior verbal and written communication to effectively communicate with customers, executives and team-members.
?Excellent Microsoft Office Suite skills to generate and maintain tracking reports.
?Excellent customer interaction skills.
?Working knowledge of databases, (Oracle is preferred) and other related database systems. Will require a person who is able to operate in an Oracle environment to generate order management interactions and reporting and to ensure an expedited transition to other internal Agilent systems for detailed record gathering.
?Previous work experience inside one of Agilent NWS?s end customers or Primes is highly desirable.
?US citizenship required
?Current US Government Security Clearance -or- ability to process for and obtain US Government Security Clearance
Position will be located in Columbia, MD. |
| Agilent Technologies, Inc. US |
Santa Rosa |
CA |
11/20/2009
|
| Semiconductor Fab Integration Engineer |
| M.S. or Ph.D. in Electrical Engineering, Physics, Materials Science, Mechanical Engineering, Chemical Engineering or equivalent experience.
Experience with advanced semiconductor and/or MEMS processes and devices is essential and specific skills in III-V device physics and processing are highly desirable.
Experience with statistical process control and design of experiments is desired.
Candidates should have excellent interpersonal, problem solving, and communication skills for successful inter-group and intra-group interactions.
US Citizenship/Permanent Resident status is 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 electronics technology.
Geo Location: Santa Rosa, CA
~cb~11/02/09 |
| Agilent Technologies, Inc. US |
Wilmington |
DE |
11/20/2009
|
| Marketing Technical Writer Intern |
| Qualifications:
- Proficient with Microsoft Word and and PowerPoint
- Strong verbal and technical writing skills.
- Strong typing skills
- Proficient and comfortable using internet and web-based tools.
cb~11/03/2009 |
| Agilent Technologies, Inc. US |
Wilmington |
DE |
11/20/2009
|
| Marketing Program Manager |
| ? Undergraduate degree in Marketing or Business Administration. Strongly prefer chemistry or Biological Sciences degree.
? Minimum of 7 years of demonstrated results in a marketing role or relevant experience
? Worldwide experience developing outbound marketing programs to drive demand for new and existing products, as well as encourage repeat purchasing
? Well developed strategic thinking skills, project management skills, experience working with outside suppliers, a proven track record of measuring and enhancing program effectiveness, strong initiative, and the ability to work with a diverse group of individuals are critical.
? Demonstrated experience developing justifications for marketing investments (ROI analysis)
? Demonstrated results orientation, including developing fact-driven, business goal-focused plans that align with strategic objectives
? Effective project management and organizational skills
? Clear and compelling writing skills; strong oral communication skills; strong content presentation skills
? Ability to work collaboratively with a diverse group of individuals cross-organizationally, cross-functionally and within a global matrix
? Strong initiative and creativity
? Experience in relationship marketing, retention, and loyalty strategies using a range of direct marketing channels
? Proven ability to understand the needs and buying influences of a scientific target audience |
| Agilent Technologies, Inc. US |
Richardson |
TX |
11/20/2009
|
| Application Engineer |
| Education:
B.S.E.E and/or M.S.E.E. preferred
Experience:
-5+ years of practical RF design engineering experience.
-2 years of which will be relevant industry experience.
-Ability to fully understand customer needs and the technical ability to fulfill them.
-Understanding of RAT's (Radio Access Technology), in 2G/3G systems like GSM, WCDMA, HSPA. WiMax, LTE and MIMO experience a plus.
-Understanding applied use of advanced one box testers, signal generators and spectrum analyzers.
Geo Location: Richardson, Texas
~cb~11/05/09 |
| Agilent Technologies, Inc. US |
Houston |
TX |
11/20/2009
|
| Service Sales Specialist ? Southern US Region |
| Requires
- BS/MS in Scientific, Engineering or Business discipline or equivalent.
- 3+ years hands on laboratory or industry experience with instrumentation hardware, software, applications coupled with industry regulatory requirements such as (GLP, GMP, FDA) highly desired
- 3+ years sales experience with a demonstrated track record of success in projects or sales at major accounts highly desired.
- Ability to translate the Value Proposition of service as a financial and operational benefit to meet customer needs.
- Strong business development, sales negotiating, and sales closing skills.
- Must have excellent communication skills (written and verbal) and teamwork skills.
- Outstanding presentation, planning and organizational skills
- High level knowledge of instrument support services business
- Computer literate with advanced skills using Microsoft suite of products (Outlook, Excel, Word, Powerpoint, Access) plus other IT systems.
- Able to interface comfortably at high levels within the customer management structure
- Demonstrated attention to detail and ability to manage large volumes of data.
- Must be available for up to 60% business travel
- Live in Houston, or surrounding communities
Region Includes: Texas, Oklahoma, Louisiana
~cb~11/09/09 |
| Agilent Technologies, Inc. US |
Schaumburg |
IL |
11/20/2009
|
| Service Technical Specialist |
| Requires higher education or specialized training/certification.
Requires a minimum of 5 years directly related calibration/repair experience, with typically 7 to 10 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) required.
Requires excellent communication and organizational skills. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| Senior Software Engineer |
| Job requirements:
? Demonstrated C/C++ programming skills in a product-development environment.
? Demonstrated knowledge of STL, MFC, ATL, ActiveX, and other related software technologies.
? Experience with Microsoft Visual Studio and other software-development tools required.
? Experience investigating newer technologies and evaluating feasibility of utilizing newer technologies for system platforms.
? Experience synthesizing a cohesive system consisting of hardware, electronics, firmware, and software.
? Ability to work collaboratively in team environments.
? Ability to provide clear and concise oral and written communication of product concepts and engineering requirements.
? Ability to follow both written and verbal directions and ask questions when necessary.
? Ability to adhere to a quality control system.
? Willingness to exercise considerable independent judgment.
? Demonstrated strong follow-through with thorough attention to detail.
Education/Experience:
? Bachelor's degree in computer science, engineering, or related field. Advanced degrees are strongly preferred.
? 10+ years of technical experience required, with past work on product-development teams strongly preferred.
? Experience developing production-quality software required, with robotics and automation experience a plus.
~cb~10/29/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| Software Engineer |
| Educated to at least university degree level, you'll also have 5+ years' practical R&D experience, including at least 3 years' in a similar environment. A keen problem-solver with a proactive, team-oriented approach, you'll relish the challenges this pioneering environment presents.
~cb~10/29/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| Software Engineer |
| Educated to at least university degree level, you'll also have 5+ years' practical R&D experience, including at least 3 years' in a similar environment. A keen problem-solver with a proactive, team-oriented approach, you'll relish the challenges this pioneering environment presents.
~cb~10/29/09 |
| Agilent Technologies, Inc. US |
Newport |
DE |
11/20/2009
|
| Chemical Process Engineer |
| Qualifications
Minimum of 4 years experience in chemical process manufacturing
Bachelors or Masters Degree in chemical engineering or chemistry
Demonstrated ability to apply chemical process fundamentals
Extensive cross-functional team experience with demonstrated excellent teamwork skills
Demonstrated success with process transfer and scale-up from R&D
Previous manufacturing experience in an ISO9000 environment
Demonstrated success improving process performance with respect to quality, rate, and yield
Proven ability to find successful solutions to multiple problems of varying scope and complexity
Demonstrated ability to work across multiple functions leading and managing projects
Excellent written and oral communication skills
Desired Qualifications:
5 to 8 years of experience
Experience with batch chemical processing
Experiences applying LEAN principles in a manufacturing environment
Experience with colloidal science - experience with colloidal silica a plus
Experience working within a Six Sigma organization with Green Belt or Black Belt certification
~cb~10/28/09 |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
11/20/2009
|
| R&D Mechanical Engineer - Intern |
| - Bachelors Degree or Masters Degree in ME in progress with a Graduation Date of May 2011 to May 2012.
- Experience via course work or previous internships
- Strong written and verbal communication skills.
- Excellent teamwork skills.
- Self-starter. Willing and able to quickly learn new technologies.
cb~10/27/2009 |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
11/20/2009
|
| R&D Electrical Engineer - Intern |
| - Bachelors Degree or Masters Degree in EE in progress with a Graduation Date of May 2011 to May 2012.
- Experience via course work or previous internships
- Strong written and verbal communication skills.
- Excellent teamwork skills.
- Self-starter. Willing and able to quickly learn new technologies.
cb~10/27/2009 |
| Agilent Technologies, Inc. US |
Columbia |
MD |
11/20/2009
|
| Advanced Programs Development Manager |
| Bachelors or Master Degree in Technical/Engineering discipline or equivalent, plus a minimum of 8 years relevant experience in RF System sales. Post-graduate and/or certification/license is a plus. Chosen candidate will possess the following:
? Experience selling RF Surveillance Products and Programs
? Knowledge of Intelligence Community and RF Surveillance competitors
? Experience in SIGINT (Signal Intelligence)
? Must be a US citizen
? Must hold or be eligible to receive SCI clearance.
? Proven experience developing complex sales strategies
? Proven track record in large system sales/High dollar revenue generation
? Experience developing relationships with Federal Government, Department of Defense, Intell organizations
? In depth product knowledge of signal generators, network analyzers, spectrum analyzers, and communications test equipment
? Skilled at working with geographically dispersed teams.
? Strong interpersonal networking and communication skills, extremely customer oriented |
| Agilent Technologies, Inc. US |
Folsom |
CA |
11/20/2009
|
| Manufacturing Operator |
| The successful candidate will possess the following:
-Ability to work with small volumes of chemicals a 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
-Skill to multi-task and organize thoughts as needed
-Capacity to lead and motivate others
-Ability to work independently and within a team
-Talent for establishing and maintaining 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
-At least 3 years experience working in a manufacturing environment
-Experience with lean manufacturing and 6-Sigma preferred
Geo Location: Folsom, CA
~cb~10/26/09 |
| Agilent Technologies, Inc. US |
Folsom |
CA |
11/20/2009
|
| Manufacturing Operator |
| The successful candidate will possess the following:
- Ability to work with small volumes of chemicals a 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
- Skill to multi-task and organize thoughts as needed
- Capacity to lead and motivate others
- Ability to work independently and within a team
- Talent for establishing and maintaining 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
- At least 3 years experience working in a manufacturing environment
- Experience with lean manufacturing and 6-Sigma preferred
~cb~10/26/09 |
| Agilent Technologies, Inc. US |
Folsom |
CA |
11/20/2009
|
| Manufacturing Operator |
| The successful candidate will possess the following:
- Ability to work with small volumes of chemicals a 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
- Skill to multi-task and organize thoughts as needed
- Capacity to lead and motivate others
- Ability to work independently and within a team
- Talent for establishing and maintaining 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
- At least 3 years experience working in a manufacturing environment
- Experience with lean manufacturing and 6-Sigma preferred
~cb~10/26/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| LC/MS Research |
| Required qualifications:
? Recent Ph.D. degree in chemical or biological sciences
? Familiarity with HPLC/MS technologies.
? Demonstrated proficiency in laboratory research.
? Ability to quickly learn and develop new laboratory skills and techniques.
? Preference to work within a multidisciplinary team and with leading edge external collaborators.
The following additional skills are highly desired:
? Experience in nanoLC/MS and its applications.
? Proficiency using high level programming languages for data acquisition, analysis and instrumentation control.
? Exceptional skills in quantitative data analysis.
? Excellent communication skills.
~cb~10/26/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| SAP Technical Lead, Expert |
| ? Proven ability to develop plans and lead technical teams in the delivery of IT projects and services.
? Demonstrated knowledge and proficiency of the Basis aspects of complex SAP environments and integration with other platforms and technologies.
? Demonstrated ability to manage large IT/business projects and programs through all phases of the project life cycle, including 3rd party resources.
? Participated in two or more full project life cycle implementations of various SAP modules.
? Demonstrated skills and proficiency of the SAP Netweaver environment with SAP ECC, CRM, APO, and BI.
? High level of understanding of eSOA and enterprise portal.
? Extensive hands on exposure to SAP environment planning, monitoring, and optimization tools.
? Excellent written and verbal communication skills in English; ability to present complex information in a clear and structured way; ability to work at all levels in the organization (end users to executives, IT and business).
? Bachelors Degree in Information Systems or Computer Science, with a focus on business applications and Information Technology. Advanced degree is preferred. Minimum of 10 years in an SAP environment, including 5+ years of technical team lead experience.
~cb~10/23/09 |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
11/20/2009
|
| R&D Software Engineer |
| Position requires:
? BS/MS Degree in Computer Science or equivalent and a minimum of 5+ years SW development experience
? 5+ yrs Java Development, with a significant portion of this in the client server area.
? Experience with Object and data modeling
? Experience with WEB application development
? Experience creating UI?s using FLEX Builder.
? Experience working with XML and XSD?s.
? Experience with database access and database design.
? Excellent verbal and written communication skills
? Ability to work with cross-functional global teams
? Results-oriented and track record of success in delivering to critical project deadlines
? Strong sense of initiative and ability to work autonomously
These additional skills are strongly preferred:
? Network protocol knowledge and experience
? Experience with multi-threaded transaction systems
? Linux OS experience
? Telecom or general networking industry knowledge is helpful ( as related to network quality of service)
? Web based transactions (managing sessions, persistence of the data, JPA)
? Knowledge of, REST API, GUI human factors background is an added plus
? C++ programming
? Prefer experience will some or all of the following: JUnit, MySql, Hibernate, JMS, XML and Java parsers, J2EE, JTA, JMX, Java Patterns.
~cb~8/18/2009 |
| Agilent Technologies, Inc. US |
MiamiTampa |
FL |
11/20/2009
|
| Academic Sales Account Manager-Florida |
| Requires
- BS/MS in a Life Science discipline (advanced degree preferred) and
- 3+ years direct sales 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
Geographic Location: Tampa/Miami |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| 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:
? 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)
~cb~10/19/09 |
| Agilent Technologies, Inc. US |
Columbia |
MD |
11/20/2009
|
| Sr. Systems Design Engineer |
| The position requires a BSEE/MSEE with emphasis in digital signal processing (DSP). Must have proven ability to use computer tools for simulation, coding and measurement (i.e. MatLab) and working knowledge of C and/or C++ languages within Microsoft Windows? and Linux operating system frameworks. Ability and desire to work on rapid paced projects with several design tasks. Ability to work effectively as a member of a geographically dispersed team of engineers both in our core labs and in other functional areas including our sales group. Chosen candidate must have excellent communication skills, both verbal and written. Must be willing to travel when necessary.
? Must be a US Citizen
? High-level government security clearance is required
Desired Skills:
? MSEE with emphasis in communications signal analysis and processing
? In-depth knowledge of programming with Visual Studio? and Wind River DIAB development environments
? Experience in design of demodulators including digital PLL's, digital filters and bit coding/decoding algorithms
? In-depth knowledge of complex receiver and signal processing chains
? Working knowledge of the Agilent E3238s system
? Knowledge of measurement techniques and considerations in the wireless market
? Working knowledge of direction finding |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| Human Resources Business Partner |
| ? BS/MS Degree in Business/ HR/OD or equivalent
? 8 years business experience in progressively challenging responsibilities in the following areas: leadership development of senior business team, organizational development/effectiveness, consulting, change management and talent management.
? A minimum of 3-5 years of HR experience within the Life Sciences space.
? Experience supporting Life Sciences channels preferred.
? A working knowledge of general HR practices a must along with the ability to influence HR strategy and policy using previous knowledge and experience from other business and work environments.
? The successful candidate will be an experienced business and human resources professional who has had experience within a heavily matrixed organization. This candidate will have related industry experience in the life science/biotech industry, with an emphasis in strategic planning, the ability to facilitate and relate to people across cultures and levels, and proven leadership skills.
Geo Location: San Francisco/Bay Area |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| Applications Scientist - Microarrays & QPCR |
| Key Areas of Expertise:
Must have expertise in the following key areas:
-Microarrays ? Agilent arrays: Gene Expression, ChIP-on Chip, CGH
-QPCR ? both probe and SYBR Green assay experience desired
-Agilent Bioanalyzer
-Use of bioinformatics software, such as GeneSpring or ArrayAssist to analyze microarray data
Education/Experience:
?Must have a B.S. or M.S. in Biology, Molecular Biology, or Biochemistry. A PhD is preferred.
?5 years lab experience with microarrays and QPCR
?Lab experience with Stratagene and Agilent products is a plus
?Must be a team player
?Excellent verbal and written communication, organizational, and project management skills
-Ability to interface with global multidiscipline internal/external cross function teams
-Ability to demonstrate excellent outbound phone calling communication skills.
-Ability to solve a broad range of problems of varying scope and complexity.
-Proactively acts to understand customer needs and identify solutions to non-standard tasks/queries; actively creates business opportunities.
Geo Location: May reside in the Santa Clara, CA - La Jolla, CA - or Wilmington De Office
No relocation assistance available.
cb~10/08/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| Product Marketing Engineer |
| ? Bachelor of Science in biology, biochemistry, molecular biology, bioinformatics, or related discipline is required. Master or PhD preferred.
? Ability to communicate and discuss technical information on copy number and SNP analysis/bioinformatics, genetics, and genomic studies.
? Knowledge of key software platforms for genetic analysis and bioinformatics tools and databases such as the eArray, DGV, NCBI and UCSC Genome Browser.
? Exceptional cross-functional communication skills - proven ability to influence at all levels of the organization.
? 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. |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
11/20/2009
|
| PC Design Intern |
| Completion of sophomore year at an accredited 4 year engineering school. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| Regional Government Security Manager (West) |
| - MUST currently hold a SCI level security clearance with a current Single Scope Background Investigation (SSBI).
- Must have a firm understanding of the security policies, procedures and directive of the DoD, National Industrial Security Program and Intelligence Community SCI security programs.
- Bachelors Degree in Criminal Justice, Security Management, Industrial Security, Business Management or equivalent combination of education and experience.
- 5 to 10 years of experience in the Government Security Field.
- Knowledgeable in the use of JPAS, DIAS COMSEC and DoD/OPM Electronic Personnel Security Questionnaire software packages.
- Proficiency with Microsoft Office products is essential.
- Requires the ability to make sound decisions, manage time, take independent action, analyze problems and provide focused solutions.
- Demonstrated ability to effectively communicate information to various audiences and all levels of the organization both verbally and through written communications.
- Must be highly organized, be willing to work in a team environment, be able to prioritize tasking, perform in a multi-tasked and dynamic environment.
- Must be dependable, responsive, customer focused and possess the qualities of diplomacy, tact, excellent judgment, discretion and initiative.
~cb~10/05/09 |
| Agilent Technologies, Inc. US |
Boulder |
CO |
11/20/2009
|
| Quality Control Analyst |
| This is a solutions oriented environment where your energy, enthusiasm and pro-active approach will not only help drive Agilent's continued growth and development, but also your own career success.
EDUCATION and/or EXPERIENCE
Bachelor's degree (B.S.) or equivalent in chemistry or related life sciences field; and five to ten years related experience and/or training; or equivalent combination of education and experience. Five to ten years experience working in a GMP production environment is required.
1. Knowledge of GMP guidelines as well as international regulations pertaining to the production of APIs and drug products.
2. Knowledge and understanding of the oligonucleotide manufacturing or related pharmaceutical manufacturing processes.
3. Skill in communication, written and verbal; will be handling various relations issues and will be confronted with various interactions
4. Knowledge of and skill in using computer software and hardware applications, including Microsoft products and the Internet.
5. Skill in managing various projects; must be able to use individual discretion in completing work assignments; while assisting the group in establishing priorities, setting standards and working collectively to accomplish deadlines and objectives
6. Ability to read, analyze, and interpret industry related periodicals, SOPs, and government regulations. Ability to write reports, business correspondence, and procedures. Ability to respond to common inquiries or complaints from customers, co-workers, subordinates, and supervisors regarding the products and processes.
Geo Location: Boulder CO
cb~11/11/09 |
| Agilent Technologies, Inc. US |
FolsomMenlo ParkPalo AltoPleasantonRedwood CityRohnert ParkRosevilleSan FranciscoSan JoseSanta ClaraSanta Rosa |
CA |
11/20/2009
|
| Instrument Firmware Developer |
| Requires:
BS degree in EE, CS or equivalent; MS is preferred - 5+ years of experience in an instrument firmware development role. Experience designing analytical equipment is strongly desired.
- Strong skills in programming to include most of the following:
o VxWorks
o Linux and/or Unix
o C, C++
o Assembler
o DSP
o Signal Processing
o Programmable Logic Design (FPGA)
o Network programming (TCP/IP, OSI layer model etc.)
- Strong skills in interfacing with analog and digital electronics:
o System architecture and design
o Communications protocols
o Driver development
o Display and keyboard protocols
- Other desired skills:
o Experience in IC design
o Experience in PCA/PCB design
o Experience in Analytical Instruments
- Good communication and documentation skills.
- Works effectively in a multi-disciplined environment and with other functions (manufacturing, marketing, etc). |
| Agilent Technologies, Inc. US |
Boulder |
CO |
11/20/2009
|
| API Process Development Scientist |
| Requires:
- 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
~cb~10/20/09 |
| Agilent Technologies, Inc. US |
AnaheimEl SegundoFolsomGarden GroveLa JollaMenlo ParkPalo AltoPleasantonRedwood CityRohnert ParkRosevilleSan DiegoSan FranciscoSan JoseSanta BarbaraSanta ClaraSanta RosaWestlake Village |
CA |
11/20/2009
|
| Product Marketing Engineer |
| ? Bachelor of Science in biology, biochemistry, molecular biology, bioinformatics, or related discipline required. Master or PhD preferred.
? Understanding of software tools used in copy number and SNP studies
? Ability to communicate and discuss technical information on copy number and SNP analysis/bioinformatics, genetics, and genomic studies.
? Knowledge of key software platforms for genetic analysis and bioinformatics tools and databases such as the eArray, DGV, NCBI and UCSC Genome Browser.
? Exceptional cross-functional communication skills - proven ability to influence at all levels of the organization.
? 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.
cb~10/01/09 |
| Agilent Technologies, Inc. US |
Santa Rosa |
CA |
11/20/2009
|
| R&D Engineer, Software |
| ? University degree in Electrical Engineering (MS level) required, PhD. in the EM simulation area highly preferred.
? Thorough understanding of EM simulation techniques, particularly in time domain methods, as well as their software implementation aspects, including the implementation of complex numerical algorithms.
? Good understanding on the application areas of EM simulation products.
? Experience in numerical/scientific programming in C/C++ and generally good software development skills
? The ability to work in a multi-site, multi-cultural team environment |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| Nucleic Acid Chemist - Genomics R&D |
| Qualifications :
? Ph.D. degree in Organic Chemistry, Biochemistry or equivalent
? 4+ years relevant experience in industry and/or academia
? Strong theoretical knowledge and hands-on applications of modern Nucleic Acid chemistries required
? Strong knowledge and experience developing DNA and RNA synthesis processes is highly desired
? Knowledge of Chemical and Physical property Analytical techniques is highly desired, including LC/MS, NMR, viscosimetry, tensiometry, etc.
? Knowledge of Surface chemistry and surface analytical techniques a plus
? Proficiency in molecular biology techniques (electrophoresis, enzymatic assays, ?) and experimental troubleshooting a plus
? Proficiency with PCR & qPCR methodologies a plus
? Previous experience with microarrays and a working knowledge of statistical methods a plus
? Computer literacy and hands-on experience working with database software applications
? Excellent communications skills and time management skills
? Ability and enthusiasm to work in a collaborative team environment
~cb~11/12/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| LC/MS Proteomics Scientist |
| PhD Degree or equivalent in Chemistry, BioChemistry, Biology, or related field.
Minimum of 4 years relevant experience.
The successful person for this position will:
? Be comfortable with all aspects of LC/MS analysis of proteins: sample preparation, instrument operation, data analysis, and data interpretation and processing
? Have the ability to use mathematical, theoretical modeling and software tools to develop predictive models for improving methods and data mining algorithms
? Have an understanding of the use of statistics in data interpretation and experimental design
? Be well-versed in the scientific method
? Have an understanding of mass spectrometry instrumentation, ion optics, and sources
? Have familiarity with and the ability to write software tools to assist in data mining
? Have a good understanding of proteomics in relation to other aspects of systems biology
? Be an effective communicator and team player
~cb~11/12/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| Applications Engineer |
| Requires:
- BS in biology, biochemistry, molecular biology; related discipline or equivalent. Master or PhD preferred.
- 3+ years experience with life science software products
- Experience with systems biology software products
- Experience in interacting with customers in a pre-sales and/or post sales support role
- Experience in generating and presenting technical training materials
- Experience in interacting with cross-functional groups including sales, marketing and R&D
Geo Location: Santa Clara, California
cb~09/11/09 |
| Agilent Technologies, Inc. US |
Boulder |
CO |
11/20/2009
|
| Process Engineer |
| B.S. Chemical Engineering
9+ years of experience in chemical or pharmaceutical manufacturing.
5+ years of experience in pharmaceutical industry with a thorough understanding of GMP production standards and compliance guidelines.
Ability to generate and review PFDs, P&IDs, facility layouts, standard operating procedures, user requirement specifications and validation documentation including installation, operational and performance qualification protocols.
Experience with current International Fire and Building Codes as well as sanitary piping design standards is preferred.
Efficient use of Microsoft spreadsheets and Word documents is required. Ability to use AutoCAD is advantageous.
Must be able to lift 50 pounds.
Geo Location: Boulder, CO
~cb~11/10/09 |
| Agilent Technologies, Inc. US |
|
MA |
11/20/2009
|
| Account Manager-Life Science Research |
| - BS/BA Degree or equivalent in molecular biology or equivalent
- 1+ years research experience
- 3+ years related direct life science product sales experience with a demonstrated track record of successfully selling against a quota.
- Demonstrated business development and sales closing skills.
- Good written and verbal communication skills.
- Ability work within a team selling environment.
- Ability to interface with all levels within an organization for both internal/external customers.
- Experience with pharmaceutical, biotech and academic customers a plus.
Geo Location: Cambridge, MA
~cb~09/09/09 |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
11/20/2009
|
| R&D Network Engineer |
| This role requires a well rounded, hands-on Network Engineer who will function as a Network expert, Software development engineer, and Test Engineer. The individual must possess a BS Engineering ( or equivalent) and possess advanced knowledge in a high-performance datacenter with direct support and network services engineering responsibilities. Network certifications are strongly preferred. C++ and XML Software development skills are also strongly preferred. Other key skills:
? Advanced experience with configuration and support of Cisco routers and switches (minimum 7+ years)
1.Desired Cisco hardware knowledge with platforms 6500, 7500, 4500, 3800, 3700, 2900
? Advanced experience with configuration and support of Hewlett Packard switches (minimum 5+ years)
1.Desired Hewlett Packard knowledge with platforms Procurve 4000m/8000m, 3400, 3500, 5300, 5400
2.Advanced experience with configuration and support of Juniper equipment.
3. Advanced experience with configuration and support of Alcatel-Lucent equipment.
? Strong layer 2 and layer 3 experience with a focus on enterprise and data center switching and routing including: Ethernet, Spanning Tree, VLAN, MPLS, Link Aggregation, ether-channel, QoS, 802.1Q, DHCP, ARP, RARP, IGMP, SNMP, IPv4, VoIP, multicast routing protocols, 10 Gig Ethernet, minimum 5 years
? Demonstrated ability to gather design requirements or problem requirements and recreate infrastructure so that initial design validation can be completed or in the case of a problem being able to troubleshoot and isolate root cause.
? In-depth knowledge of network element infrastructure, error reporting, OS limitations, etc.
? Strong Customer interface skills
? Excellent written and communication skills
? Experience in mentoring peers and junior level engineers and administrators
~cb~8/31/2009 |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
11/20/2009
|
| R&D Software Engineer |
| Position requires:
? BS/MS Degree in Computer Science or equivalent and a minimum of 5+ years SW development experience
? 5+ yrs Java Development
? Linux OS experience
? Telecom or general networking industry knowledge is helpful ( as related to network quality of service)
? Experience with WEB application development
? Knowledge of FLEX GUI Builder, REST API, and XML/XSD, GUI human factors background is an added plus
? Excellent verbal and written communication skills
? Ability to work with cross-functional global teams
? Results-oriented and track record of success in delivering to critical project deadlines
? Strong sense of initiative and ability to work autonomously
These additional skills are strongly preferred:
? Experience with Object and data modeling
? Web based transactions (managing sessions, persistence of the data, JPA) |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
11/20/2009
|
| R&D Software Engineer |
| Position requires:
? BS/MS Degree in Computer Science or equivalent and a minimum of 5+ years SW development experience
? 5+ yrs Java Development
? Experience building devkits is preferred
? C++ experience desirable
? Linux OS experience desirable
? Telecom or general networking industry knowledge is helpful ( as related to network quality of service)
? Experience with WEB application development
? Knowledge of FLEX GUI Builder, REST API, and XML/XSD, GUI human factors background is an added plus
? Excellent verbal and written communication skills
? Ability to work with cross-functional global teams
? Results-oriented and track record of success in delivering to critical project deadlines
? Strong sense of initiative and ability to work autonomously
These additional skills are strongly preferred:
? Experience with Object and data modeling
? Web based transactions (managing sessions, persistence of the data, JPA)
~cb~8/27/2009 |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
11/20/2009
|
| R&D Software Engineer |
| Position requires:
? BS/MS Degree in Computer Science or Human Factors Engineering or HCI with a minimum of 5+ years experience working as a Human Factors Engineer on software products
? Experience with User Interface Design and Usability is a must
? Experience developing User Interface software is a must.
? Expertise in HCI/UI/Usability standards and de-facto standards is preferred
? Excellent verbal and written communication skills
? Ability to work with cross-functional global teams
? Results-oriented and track record of success in delivering to critical project deadlines
? Strong sense of initiative and ability to work autonomously |
| Agilent Technologies, Inc. US |
Columbia |
MD |
11/20/2009
|
| System Architect |
| Qualifications:
Qualifications:
? Bachelors or Master Degree or University Degree in Electrical/Electronic or Computer Engineering and 5+ years applicable experience in architecting and implementing complex software solutions, and a deep understanding of Mobile Communication Systems and Networks. (Including Cell Phone and other Mobile Communications Infrastructure).
? Software project management, definition, development and deployment expertise.
? Understanding of the customers data streams and architecture where our products content will be used.
? Direct experience with SIGINT customers, products and applications.
? Experience in SIGINT acquisition systems, familiarity with content acquisition platforms in wireline, cellular telecom, and IP.
? End USER expertise in SIGINT missions
? Experience with end user, installation and commissioning of new systems within customer environments is highly desired.
? Familiarity with 7 layer OSI model and current and evolving telecoms standards including Wireless Protocols, with a strong background in IP
? Self starter and ability to self-learn
? Strong interpersonal/relationship skills, solid written and verbal communications
? US citizenship required.
? Current US Government Security Clearance -or- ability to process for and obtain US Government Security Clearance |
| Agilent Technologies, Inc. US |
Wilmington |
DE |
11/20/2009
|
| 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 |
New Castle |
DE |
11/20/2009
|
| Logistics Representative-Advanced Level |
| Must Skills:
Undergraduate and/or MBA in Logistics or Supply chain or Business. Demonstrated strong written, verbal and presentation skills
Project management experience desired
Knowledge/ understanding of demand management/logistics and supply chain management concepts
Excellent personal computer skills
Financial, Analytical and statistical skills to resolve complex supply chain process/system problems
Demonstrated ability to influence others, strong planning and organizational skills, and work effectively across groups/ work teams with varying skill sets and backgrounds.
Working knowledge of ERP Systems - SAP/ MS applications, Excel, MSaccess, project, database creation/management a Plus |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
11/20/2009
|
| Network and Service Assurance Product Planner/Product Manager |
| ?? Bachelors or Master Degree or University Degree or equivalent plus a minimum of 5 years relevant experience in product planning and strategy, with typically 10 or more years of practical experience through which you have developed an in-depth knowledge both technical and marketing in the mobile/wireless and wireline market segments.
? Expert knowledge of performance monitoring / assurance systems for multi-service communications networks
? Teamwork and communication skills are a requirement as you work directly with customers, sales channel, applications engineers, business development, R&D and senior management.
? Specific Requirements:
o Proven product planning or product architect results and experience.
o Excellent understanding of wireless and wireline technologies [e.g. IMS, LTE, WiMAX, Triple Play]
o Knowledge and experience of wireline transport and mobile communication networks, their operation, and interworking.
o Knowledge and experience of the key issues faced by network operators as they deploy and manage telecom networks and services
o Experience in working with network operators. |
| Agilent Technologies, Inc. US |
Anaheim |
CA |
11/20/2009
|
| LCMS Product Specialist-Los Angeles |
| ? Strategic Selling Skills (Executive Selling, Solution Selling)3-5 years
? High degree of LCMS application and platform domain competency
? Strategic Selling Skills (Executive Selling, Solution Selling)3-5 years
? LCMS Industry and Market Knowledge
? Excellent Verbal and Written Communication Skills as well as Interpersonal and Presentation Skills
? Teaming/Collaboration Skills (resource mgmt. and team leadership)
? B.S., M.S. or PhD in Biology, Chemistry, or Molecular Biology
~cb~09/09/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| NPI Engineering - Mass Spectrometer Instrumentation |
| Requires:
- BS/MS degree in Electrical Engineering or equivalent
- 2+ yrs industry experience working on the NPI of large integrated systems
- Experience in bringing new product design from R&D to scalable manufacturing
- NPI experience of Mass Spectrometer Instrument Systems highly desired
- knowledge of electrical theory, components, and circuits
- Experience with high voltage components desired
- Knowledge of PCA test methods
- Excellent written and verbal communication skills
- Track record of success working within cross functional /cross regional teams
- DFX Experience
- Available for up to 10% business travel
Geo Location: Santa Clara, CA
~cb~8/17/2009 |
| International Partnership for Microbicides, Inc. |
|
Paarl |
11/20/2009
|
| Clinical Medical Director |
| Education/Experience
- Degree in Medicine from a tertiary institute and medical specialty preferred;
- Minimum of 10 years in clinical research environment or relevant setting;
- Minimum 5 years in pharmaceutical industry clinical research, pharmacovigilance or Medical Affairs or equivalent;
- Registration with the relevant Medical Council;
- Previous experience in the safety field and/or pharmaceutical industry;
- Experience in Clinical Medicine and Familiarity with Ethical Practices.
Knowledge, Skills, and Abilities
- Must have knowledge of Pharmacovigilance, clinical safety regulations and guidelines, and clinical research trials methodology, design, implementation and analysis;
- Must have knowledge of FDA Regulations, EMEA Regulations, ICH GCP guidelines, Local Regulations of the country where trials are being conducted, and clinical trials research and management;
- Knowledgeable and skilled in medicine and pharmaceutical product safety;
- Experience applying medical knowledge to the interpretation of individual case review;
- Experience with reporting of individual adverse events;
- Have the ability to comprehend, integrate and interpret scientific and medical data from a variety of resources;
- Experience working in a team environment, including supporting other team members when necessary promote collegiality and teamwork among peers;
- Ability think clearly and decisively and present independent, reasoned solutions to identified safety issues, helps to drive consensus of opinion, and catalyzes action to meet critical regulatory objectives;
- Demonstrated creative problem solving skills that enact change and drive continuous improvement;
- Seeks to develop self and others;
- Excellent oral, and written skills;
- Excellent communication, interpersonal and time management skills;
- Demonstrated flexibility and adaptability in a rapidly changing environment;
- Ability to build and manage inter-relationships by motivating and inspiring others.
Terms and ConditionsThis position is based in the Clinical Affairs Department in South Africa IPM office. Job holder should expect fast-paced working environment. International Travel required (at least 50%). A valid driver's license and own reliable vehicle is required. |
| International Partnership for Microbicides, Inc. |
|
Paarl |
11/20/2009
|
| Community Engagement Director |
| Education/Experience
- A Masterâ??s degree or higher in health education, community development, public health or related field is required for this position.
- Extensive experience in international and national community education, project management and stakeholder engagement.
Knowledge, Skills, and Abilities
- Strong team leadership, strategic planning, problem solving and conflict resolution skills.
- Demonstrated ability to work with diverse communities and exhibit cultural sensitivity.
- Familiarity with and sensitivity to perspectives and concerns among HIV-affected communities. Fundamental working knowledge regarding the scientific, ethical and other aspects of microbicide evaluation will be an advantage.
- Ability to communicate successfully with a variety of constituencies, including professional and clinical staff in national and international organizations, senior government officials and researchers, as well as community leaders and trial participants.
- Understanding of issues and organizational structure of HIV prevention and services at the community level.
- End-user computer efficiency, with proficiency in Microsoft Office products.
- Ability to motivate and influence others, and maintain positive interpersonal relationships;
- Ability to organize and prioritize multiple projects and tasks.
- Excellent verbal and written skills; must be able to communicate effectively at all levels of the organization.
- Ability to work independently and in a cross-functional and cross cultural team environment;
- Good conflict resolution and problem solving skills.
This position is based in the Clinical Affairs Department in Paarl, South Africa. Job holder should expect fast-paced working environment. International Travel required (at least 50%). |
| International Partnership for Microbicides, Inc. |
Silver Spring |
MD |
11/20/2009
|
| Executive Assistant |
| â?¢ Associate/Bachelorâ??s degree or equivalent experience working in position with similar responsibilities.
â?¢ Minimum five years administrative experience assisting senior level executives with demonstrated experience in positions that require maturity, poise, ability to handle sensitive information and communicate with high level stakeholder and constituents.
General office in downtown Silver Spring, Maryland. Job holder should expect fast-paced, dynamic working environment.IPM is an Equal Employment Opportunity Employer. |
| International Partnership for Microbicides, Inc. |
|
Paarl |
11/20/2009
|
| Laboratory Monitor |
| Education/Experience
- Minimum of a Biotechnology degree or equivalent;
- Minimum of 3 yearsâ?? experience in clinical research and laboratory setting will be a preference;
- Good knowledge of Good Laboratory Practice (GCP) will be a preference;
- Experience working in an accredited laboratory;
- Experience in SOP writing;
- Willingness and ability to travel as required (typically requires 60% travel);
- Ability to motivate and mentor, maintain positive interpersonal relationships;
- Familiarity with HIV/AIDS and/or Africa medical settings is desired.
Knowledge, Skills and Abilities
- Demonstrated proficiency in Microsoft Office products, including Word, PowerPoint and Excel, as well as web-based research and information collection skills required.
- Excellent time management skills. Demonstrated ability to organize and prioritize multiple projects and tasks.
- Initiative - highly motivated and team oriented, but also able to work independently, assessing priorities and competently handling a variety of activities with a high degree of accuracy in a deadline-driven environment.
- Strong written and verbal communication skills; must be able to communicate effectively.
- Superior attention to detail â?? is thorough when performing work and conscientious about every aspect of work.
- Results orientation - ability to work in a fast-paced environment and meet deadlines with competing priorities.
Terms and ConditionsThis position is based in the Clinical Affairs Department in Paarl, South Africa. Job holder should expect fast-paced working environment. International travel required (60%). |
| International Partnership for Microbicides, Inc. |
|
Paarl |
11/20/2009
|
| Medical Writer |
| Education/Experience
- Relevant tertiary education.
- Proven experience in medical and regulatory writing and editing.
- Experience with regulatory documents for a pharmaceutical company or clinical research organization.
- Must be familiar and up-to-date on regulations such as ICH guidelines and current good clinical practices.
- Must have experience and significant participation in preparation of clinical documents for regulatory submissions
- Experience in incorporating diverse feedback into a high quality document.
Knowledge, Skills, and Abilities
- Exceptional attention to detail
- Excellent verbal and written communication skills
- Demonstrated expertise with grammar, syntax, and format
- Systematic, methodical and process driven
- Ability to work precisely according to procedures, rules and regulations
- Ability to approach issues from a number of perspectives, summarizing data to draw a conclusion.
- Ability to work unsupervised taking responsibility for own actions
- Proficiency in word processing systems, i.e., Microsoft Word, MS Office or similar systems.
This position is based in the Clinical Affairs Department in Paarl, South Africa. Job holder should expect fast-paced working environment. |
| International Partnership for Microbicides, Inc. |
|
Paarl |
11/20/2009
|
| Site Development Coordinator |
| Education/Experience
- Bachelors degree in life science or healthcare field, or equivalent;
- Minimum of three (3) years experience in clinical research;
- Good knowledge of regulatory and ICH/GCP guidelines required;
- End-user computer efficiency, with proficiency.
Knowledge, Skills and Abilities
- Demonstrated proficiency in Microsoft Office products, including Word, PowerPoint and Excel, as well as web-based research and information collection skills required;
- Demonstrated poise and maturity in communicating with high-level executives.
- Excellent time management skills. Demonstrated ability to organize and prioritize multiple projects and tasks.
- Initiative-highly motivated and team oriented, but also able to work independently, assessing priorities and completely handling a variety of activities with a high degree of accuracy in a deadline-driven environment.
- Strong written and verbal communication skills; must be able to communicate effectively.
- Superior attention to detail- is thorough when performing work and conscientious about every aspect of work.
- Results orientation- ability to work in a fast-paced environment and meet deadlines priorities.
Terms and ConditionsInternational travel required (60%). Position is based in Paarl, South Africa. |
| International Partnership for Microbicides, Inc. |
|
Paarl |
11/20/2009
|
| Site Development Manager |
| Education/Experience
- Bachelors degree in life science or healthcare field, or equivalent;
- Minimum of five (5) yearsâ?? experience in clinical research;
- Good knowledge of regulatory and ICH/GCP guidelines required;
- Willingness and ability to travel as required (typically requires 50% travel);
- Ability to motivate and mentor, maintain positive interpersonal relationships;
- Familiarity with HIV/AIDS and/or Africa/Asia medical settings is desired;
- End-user computer efficiency, with proficiency in Microsoft Office products.
Knowledge, Skills, and Abilities
- Demonstrated poise and maturity in communicating with high-level executives;
- Excellent time management skills. Demonstrated ability to organize and prioritize multiple projects and tasks;
- Initiative - highly motivated and team oriented, but also able to work independently, assessing priorities and competently handling a variety of activities with a high degree of accuracy in a deadline-driven environment;
- Strong written and verbal communication skills; must be able to communicate effectively;
- Superior attention to detail â?? is thorough when performing work and conscientious about every aspect of work;
- Results orientation - ability to work in a fast-paced environment and meet deadlines with competing priorities.
- Demonstrated proficiency in Microsoft Office products, including Word, PowerPoint and Excel, as well as web-based research and information collection skills required.
This position is based in the Clinical Affairs Department in South Africa IPM office. Job holder should expect fast-paced working environment. |
| Teva Pharmaceuticals USA |
North Wales |
PA |
11/20/2009
|
| Talent Development Specialist |
|
| Teva Pharmaceuticals USA |
North Wales |
PA |
11/20/2009
|
| Sr. Manager, Network Administration & IT Security |
|
| Teva Pharmaceuticals USA |
Horsham |
PA |
11/20/2009
|
| Sr Director, Clinical Reg Affairs- Women's Health |
|
| Teva Pharmaceuticals USA |
North Wales |
PA |
11/20/2009
|
| HR Analyst |
|
| Teva Pharmaceuticals USA |
Horsham |
PA |
11/20/2009
|
| Employment Law Counsel |
|
| Teva Pharmaceuticals USA |
North Wales |
PA |
11/20/2009
|
| Staffing Partner |
|
| Teva Pharmaceuticals USA |
Fairfield |
NJ |
11/20/2009
|
| Security Officer |
|
| Teva Pharmaceuticals USA |
North Wales |
PA |
11/20/2009
|
| Business/Market Research Analyst |
|
| Biogen Idec, Inc. |
Cambridge |
NC |
11/20/2009
|
| Supervisor, Manufacturing |
Must have Excellent GMP documentation skills. A Full understanding of bio-processing (Purification, Cell Culture, Dispensing operations, and Production support)
A Fundamental knowledge of validation is required. Must have good troubleshooting skills. Strong interpersonal, leadership and communication skills are required. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Sr. Compensation Analyst |
â?¢ Experience (5-7 years) in compensation design and analysis with strong quantitative and analytical skills.
â?¢ Preferred background will include consulting firm experience, biotech/pharma sector experience and experience in a commercial (sales and marketing) organization.
â?¢ Proven critical thinking capabilities, judgment, ethical standards and interpersonal communication skills are required.
â?¢ Ability to effectively prioritize, take initiative and consistently deliver high-quality, accurate work within deadlines is required.
â?¢ Advanced capabilities in analysis and modeling with MS-Excel and other analytic tools is required. |
| Biogen Idec, Inc. |
Washington DC |
DC |
11/20/2009
|
| Research & Support Analyst, Government Relations |
| 3-5+ years of previous relevant and related experience |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Associate Director, Public Affairs |
â?¢ Minimum 8-10 years in public relations, including agency or corporate experience
â?¢ Strong background in product PR campaigns
â?¢ Media-relations experience, particularly with consumer, health and trade media
â?¢ Excellent strategic thinking and tactical execution skills
â?¢ Excellent written, verbal and leadership communication skills
â?¢ Ability to work closely and collaboratively with counterparts in neurology marketing, as well as other members of the public affairs department, in a time-sensitive environment
â?¢ Ability to handle and manage issues and crisis scenarios
â?¢ Ability to manage outside PR agencies
â?¢ Strong initiative and ability to multi-task |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Associate Scientist II, BioPharm Develop |
â?¢Experience and expertise in crystallization and recrystallization of API to conduct pre-elementary polymorph screening.
â?¢Experience in preparing salts to conduct or support the salt screening efforts.
â?¢Experience in NMR, LC/MS and MS/MS
Education: BS/MS in Organic Chemistry
BS: 5+yrs and MS 3+yrs |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Scientist II, Stability |
Minimum of 3 years direct experience in stability / formulation of biological and/or small molecule products in the Pharmaceutical industry, with 10+ years industry experience.
PhD with 10+ years industry experience preferred, or BS/MS degree in Biology, Chemistry, Biochemistry, Chemical/Biochemical Engineering, or related disciplines with equivalent experience. |
| Biogen Idec, Inc. |
Waltham |
MA |
11/20/2009
|
| Director, Finance Syntonix |
Qualifications:
â?¢ Significant financial management experience ranging from business unit level strategic planning to detailed budgeting and decision support.
â?¢ High level of business acumen with the ability to identify key issues and questions and explain to others with diverse functional backgrounds.
â?¢ Excellent informal leadership skills with the ability to influence peers in business line functions.
â?¢ Experience working across cultures and companies to develop effective relationships and processes.
â?¢ Effective communicator with the ability to tailor message and delivery to both technical and senior audiences. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Lead, Manufacturing - Cell Culture |
Understands the theory and concepts behind biopharmaceutical technology and processes. A strong knowledge of at least one mfg. department with a general understanding of process impact on other mfg. Areas.
Demonstrates ability to recognize deviations from procedures and/or production records. Understanding of in-process specs and limits. Ability to perform validation runs independently. Must possess ability to balance outside projects with production schedule. Understands impact of validation on production.
***Must be able to work rotating shifts - 7:00am/pm to 7:00pm/am***
Education:
BS degree and minimum 6 years of manufacturing experience in a biotech setting.
Appropriate leadership and process experience may be substituted for degree. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Director, Small Molecule Product Quality Management |
Ph.D. in Chemistry, Pharmaceutical Sciences or equivalent with 10+ years of experience in Analytical Development, Process Chemistry or Manufacturing, including 3+ years in Quality or Regulatory departments of Pharmaceutical Company/ies.
Experience in working with external collaborations for manufacturing, CMC projects and matrix managed projects is desirable. The candidate should possess working knowledge of Quality Assurance, Quality Control, cGMP compliance and regulatory requirements for multiple regulated territories.
Success factors for this leadership position are ability develop people, change management, ability to drive teamwork for timely decisions in a multi-disciplinary, matrix managed results oriented environment. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Associate Director, Supply Chain Quality- Small Molecule |
-Minimum of 10 years Small Molecule experience, with at least 5 years experience in Quality Assurance.
-Understanding of cGMPs, quality systems and regulations.
-Excellent written and verbal communication skills.
Minimum of B.S. in Science or Engineering. Advanced degree preferred. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Scientist I, BioPharm Development |
â?¢Experience and expertise in HPLC, Dissolution, GC/MS (headspace for residual solvents), solid state characterization: PSD, XRPD, TGA, DSC, BET, VTI etc. This includes method development (quantitative and qualitative).
â?¢DHA: is able to write protocols and reports to conduct the compatibility testing supporting the IND and other regulatory filings.
Education: PhD in Analytical Chemistry
BS: 6+yrs, MS: 4+yrs and PhD: 2+yrs |
| Biogen Idec, Inc. |
Waltham |
MA |
11/20/2009
|
| Associate Scientist |
| A minimum of 3+ years of industrial research experience. The successful candidate should be responsible, motivated, flexible, a good team-player, have excellent oral and written communication skills, be able to collaborate with cross-functional teams. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Director, CMC - Late Stage Small Molecule |
A Ph.D. in Chemistry with 10 + years of experience in the pharmaceutical industry in areas related to CMC. Prior experience in leading CMC teams is essential. Experience with filing of an NDA and commercialization of a product would be a plus. Strong communication skills and the ability to work in a matrix environment are essential elements for this job.
a. Overall knowledge of drug development technical experience in at least one area of CMC
b. Previous experience on CMC teams and in leading cross functional teams
c. Experience in healthcare/biotech/pharmaceutical industry with a demonstrated understanding of the interdependencies of research, development, preclinical, clinical and regulatory functions
d. Demonstrated leadership and capability for strategic analysis and issue resolution. Organizational and project management skills working in a matrix environment
e. Excellent communication, negotiation, problem solving and decision making skills and a strong ability to influence or manage without direct authority |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Principal Scientist, Pathologist |
â?¢5 years of experience in toxicologic pathology is desirable.
â?¢Excellent written and spoken communication skills are expected.
â?¢Experience and proven ability to work with scientists and professionals from a wide variety of disciplines in a dynamic, project-driven environment
â?¢Desire to have impact on the development of novel pharmaceuticals |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Scientist II, BioPharm Develop |
â?¢Experience in solid state chemistry and material science technology.
â?¢Expertise in pre-formulation (characterization of physiochemical properties).
â?¢Experience in drug discovery support and solubilizing techniques to support medicinal chemistry, pharmacology, DMPK and PCDS.
â?¢Expertise in polymorphism, salt screening/salt selection |
| Biogen Idec, Inc. |
Waltham |
MA |
11/20/2009
|
| Head of Human Resources, Syntonix |
Ten to fifteen years (Post University) experience in progressively responsible roles in HR, including HR business partner or generalist role supporting a multi-function business with global scope. Experience working within both small and large company environments is a significant plus.
Possesses the business maturity and interpersonal savvy to work with senior leaders, including Executive Committee members, as well as the sensitivity to work with line employees.
Track record of driving creative solutions within a dynamic environment and the ability to lead and create positive change.
Proven ability and eagerness to achieve results by working as part of a management team is essential. To develop the trust and confidence of key line and HR staff, the candidate should have strong leadership abilities (e.g., be credible, consultative, and persuasive).
Preference will be given to candidates with experience in different HR functions, and to those with experience in a highly matrixed environment.
Individuals with demonstrated leadership capabilities in line management roles are also highly desirable, as are candidates with biotechnology and/or pharmaceutical experience. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Supervisor, Animal Facility |
â?¢Minimum of six to eight years directly related laboratory animal experience with at least three years supervisory experience
â?¢Certification/Licensure: AALAS certification at the LATG level, and CVT certification is preferred
â?¢Knowledge and experience of animal husbandry and sanitization requirements, and cagewash operations
â?¢Knowledge and experience in proper methods of small laboratory animal husbandry, handling and restraint, injection and sample collection techniques and euthanasia procedures
â?¢Advanced understanding of colony health status requirements and applicable animal care regulations
â?¢Excellent interpersonal, supervisory, and leadership skills. Demonstrated ability to interact professionally with investigators, contractors, vendors, and staff
â?¢Sound judgment and decision making skills, effective written and verbal communication and supervision skills
â?¢Excellent organizational and observational skills
â?¢Ability to work independently with minimal supervision
â?¢Advanced working knowledge of Microsoft Word and Excel
â?¢Ability to lift, push/pull 50 pounds |
| Biogen Idec, Inc. |
Waltham |
MA |
11/20/2009
|
| Clinical Program Leader |
â?¢Typically requires at least 8+ years of global drug development with experience managing clinical projects within time, budget, and quality expectations.
â?¢Experience in hemophelia, thrombosis and/or oncology clinical research and development is very desirable
â?¢NDA/BLA or MAA experience desirable, particularly within an orphan/rare disease therapeutic area.
â?¢Thorough knowledge of GCP, ICH guidelines and awareness of global regulatory requirements/differences for clinical development.
â?¢Detail and process oriented, with excellent project management skills, including risk assessment and contingency planning.
â?¢Demonstrated leadership, communication, and organizational skills, along with problem solving, conflict resolution, and team building skills.
â?¢Proven excellence in cross-functional matrix and/or cross-cultural partnership setting preferred. |
| Biogen Idec, Inc. |
Seattle |
WA |
11/20/2009
|
| Senior Program Officer - Agricultural Development |
• Minimum of ten years experience in the development and management of projects involving crop improvement, crop management, extension research and/or seed systems for Africa or South Asia
• A PhD or other advanced degree in a discipline relevant to crop improvement, including plant breeding, molecular marker applications, agronomy or a closely related field
• The capacity to think through, evaluate, justify, and make major investments in agricultural research and development
• An outstanding record of achievement and leadership in the field
• Experience developing, managing, and implementing project strategies and the negotiation, execution, conduct and management of performance-based contracts
• Experience with grants or cooperative agreements
• Ability to think/work at scale as well as “work in white space,” create new ideas, strategize with passionate commitment to a successful outcome
• Demonstrated excellent written and oral communication skills in positions requiring communication with a broad and diverse audience
• Ability to prioritize, focus, and achieve results in a fast paced environment
• Track record of working well with others in teams; sense of humor
• Selfless dedication to the mission, flexibility, and willingness to learn
• Overseas experience and the ability to travel internationally |
| Biogen Idec, Inc. |
Waltham |
MA |
11/20/2009
|
| Director, Product Development |
At least 10 years of biotech/pharmaceutical industry experience, including in program management and/or clinical development. An understanding and command of topics across manufacturing, regulatory and commercial functions is critical to success in the role. Ability to navigate a corporate organization and manage a collaboration partner with diplomacy are essential skills.
Experience in the following is a significant plus:
o hemophilia program leadership
o clinical development in hemophilia and/or in a global clinical trial
o commercial or regulatory responsibility for a program in clinical development |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Sr Manager, R&D Application Support & Training |
ï?§ Proven expertise in the management of scientific software support design, testing, production implementation, and training in a large corporate environment.
ï?§ At least 5 years of software management experience is required, with a minimum of 3-5 years of project management experience.
ï?§ Ability to effectively communicate with customers is essential.
ï?§ Excellent managerial and communication skills combined with proven ability to interact in multi-disciplinary cross-cultural project teams.
ï?§ Experience in a similar position in the biotechnology or pharmaceutical industries is preferred. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| eDiscovery Operations Manager |
| Minimum 3 years of industry experience |
| Biogen Idec, Inc. |
Wellesley |
MA |
11/20/2009
|
| Senior Manager, Marketing - Tysabri |
â?¢ Minimum 5 plus years commercial health care / prior marketing experience
â?¢ Solid understanding of key marketing principles
â?¢ Ability to manage external brand agencies and vendors on a day-to-day basis and
â?¢ Ability to manage promotional budgets
â?¢ Understand process in obtaining approval for promotional pieces materials through the medical, regulatory and legal promotional review process
â?¢ Excellent planning, analysis, project and budget management skills, with experience managing multiple projects against a timeline
â?¢ Strong interpersonal skills and the ability to work and manage cross-functional teams
â?¢ Demonstrates understanding of Pharma/Biotech commercial products, (BIIB and relevant competitor product knowledge), market dynamics and practice settings
â?¢ Detail oriented, strong quantitative and analytical ability
â?¢ Ability to understand and communicate highly scientific and technical medical information
â?¢ Must possess excellent verbal and written communication skills including strong presentation skills
â?¢ Demonstrated success in persuasion, influence, and negotiation skills
â?¢ Demonstrated business acumen
â?¢ Ability to travel up to 25%
â?¢ Prior field sales and CRM experience preferred |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Technician II, Animal Care |
â?¢ Minimum of 2-5 years directly related experience.
â?¢ AALAS certification is preferred or successful achievement of certification within 18 months of hire.
â?¢ Proficiency with basic technical procedures and identification methods.
â?¢ Good working knowledge of Microsoft Word and Excel.
â?¢ Strong organizational skills and attention to detail.
â?¢ Strong written and verbal English communication skills. Ability to follow written and verbal instructions.
â?¢ Ability to stand for extended periods of time.
â?¢ Ability to regularly lift/push, or pull up to 50 pounds.
Other
Regular work schedule is 40 hours per week; however, the incumbent may be required to work on weekends and holidays on a rotating basis. This position is over time eligible. |
| Biogen Idec, Inc. |
Pittsburgh |
PA |
11/20/2009
|
| Area Business Manager, Neurology - Pittsburgh S., PA |
| Minimum 5+ years pharmaceutical sales or biotech sales experience required. Experience with reimbursement issues, product launch, and injectable/infusion product selling experience desired. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Manager, EHS â?? R&D Support, Radiation Safety Office |
The successful candidate will also have experience in one or more of the following:
-Biosafety program - Providing oversight for the implementation and documentation of a biosafety program
-Material Safety Data Sheet program - Providing oversight to product MSDS development process
-Potent compound program â?? Supporting the implementation of an active pharmaceutical ingredient exposure control program.
-Green Chemistry â?? Developing and implementing green chemistry principles in an R&D setting.
Qualifications
Successful candidate will have demonstrated the following experience:
8-10 years working in a biotechnology or pharmaceutical environment with a good understanding of scientific principles and practices. Experience as a safety professional applying a working knowledge of regulatory requirements and dealing with relevant federal, state and local regulatory agencies.
Masters degree and Certified Health Physicist certification preferred. |
| Biogen Idec, Inc. |
San Diego |
CA |
11/20/2009
|
| Scientist II, BioPharm Develop |
| A Ph.D. in Biochemistry/Chemistry/Pharmaceutics/Chemical Engineering or a related discipline with a minimum of two years biopharmaceutical industry experience or relevant postdoctoral experience is required. The candidate should have excellent laboratory, computer, documentation, communication and organizational skills. Experience with protein formulation and analysis is required. |
| Biogen Idec, Inc. |
Cambridge |
NC |
11/20/2009
|
| Sr Clinical Logistics Analyst |
- Strong written and oral communication skills
- Ability to multitask on a daily basis and maintain multiple projects in parallel
- Proven capability to work in a fast paced dynamic environment
- Experience in a regulated industry or in an environment dealing with workflow industry contraints (i.e. ISO, ISTA, GMP, etc.)
- Prior Logistics experience
- Cold chain logistics or pharmaceutical logistics experience a plus
Education:
A Bachelor Degree in a technical discipline or Industrial Engineering is required. |
| Biogen Idec, Inc. |
Wellesley |
MA |
11/20/2009
|
| National Sales Director - East |
â?¢ 5 years of successful sales management experience in the pharmaceutical or biotech industry.
â?¢ Must have professional experience outside of sales, such as Marketing, Managed Markets
â?¢ Neurology or Specialty sales experience is highly desirable.
â?¢ Ability to work in close collaboration with multiple departments, including sales and marketing to align objectives
â?¢ Experience with systematic approach to both selling & sales procedures is needed.
â?¢ Strong leader with effective coaching and team building skills
â?¢ Solid negotiation, oral and verbal communication, organizational, presentation and analytical skills required.
â?¢ Ability and willingness to travel up to 60% of the time.
â?¢ There is flexibility as to where this position can geographically reside but it must be based within the Northeast/Mid Atlantic area |
| Biogen Idec, Inc. |
Waltham |
MA |
11/20/2009
|
| Director, Global Hemophilia Marketing |
Seasoned marketing professional, with at least 10 years of pharmaceutical commercial experience, including development and execution of a brand plan in a specialty market.
Experience in the following is a significant plus:
o hemophilia commercial strategy development
o execution on pre-launch and launch activities in hemophilia or specialty markets
o health economics expertise
o build out of infrastructure in a specialty therapeutic area new to the employer |
| Biogen Idec, Inc. |
Waltham |
MA |
11/20/2009
|
| Scientist II |
â?¢3-5 years of industry experience in (peptide/protein) analytical chemistry in a research/product development setting.
â?¢Understanding and hands-on experience with a wide range of analytical chemistry techniques: HPLC (reversed-phase, size-exclusion, ion exchange), Electrophoresis (SDS-PAGE/IEF/CE), Protein Sequencing, Peptide Mapping, Carbohydrate Analysis and Mass Spectrometry.
â?¢Knowledge and experience with amino acid post-translational modifications.
â?¢Understanding and hands-on experience with biophysical techniques: ITC and Light Scattering
â?¢Excellent oral, written and interpersonal communication skills and an ability to work across scientific disciplines.
â?¢Experience with FDA/ICH guidelines.
â?¢Knowledge of statistics and the ability to interpret experimental data to summarize the key findings.
â?¢Meticulous attention to detail in following procedures, preparing written documentation and execution of experiments.
â?¢Perform complex assays and investigate/troubleshoot assay problems. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Associate General Counsel, IP |
This position is targeted for 12+ years minimum post-law school experience. Experience in a law firm and a pharmaceutical/biopharmaceutical corporation is strongly preferred. Substantial experience with supporting business development activity and intellectual property strategy is required.
Substantial experience with freedom to operate analysis and opinion work is also required. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Manager, Business Analysis |
| Prior project management and operations experience are required. |
| Biogen Idec, Inc. |
Raleigh/Durham |
NC |
11/20/2009
|
| Scientist I, Stability |
Minimum of 3 years direct experience in stability / formulation of biological and/or small molecule products in the Pharmaceutical industry, with 6+ years industry experience.
PhD with 6+ years industry experience preferred, or BS/MS degree in Biology, Chemistry, Biochemistry, Chemical/Biochemical Engineering, or related disciplines with equivalent experience. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Associate II, Quality Control - Virology |
At least 5 years of related experience or equivalent combination of education and experience, previous Quality Control and GLP experience required. Viral clearance/vaccine production experience strongly preferred. Will consider candidates without virology experience if other technical requirements are met (PCR, bioassay, cell culture, etc.)
BS in a Biological Science or related technical field. |
| Biogen Idec, Inc. |
Waltham |
MA |
11/20/2009
|
| Associate Director, Global Hemophilia Marketing |
Seasoned marketing professional, with at least 8 years of pharmaceutical commercial experience, including global marketing and market research in a specialty therapeutic area.
Experience in the following is a significant plus:
o hemophilia commercial marketing and/or sales
o execution on pre-launch and launch activities in hemophilia or specialty markets
o health economics strategy and execution |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Director, Discovery & Preclinical IT |
â?¢ In-depth knowledge of informatics and IT solutions in the discovery and preclinical space.
â?¢ Proven expertise in global solutions design, development, and production implementation.
â?¢ Excellent managerial and operational skills, combined with strong customer focus.
â?¢ Ability to effectively communicate with peers, upper management, and business partners
â?¢ Demonstrated ability to articulate and â??sellâ? a vision for IT-enabled drug discovery.
â?¢ Proven ability to lead multi-disciplinary, cross-cultural project teams.
â?¢ Comfortable working in a matrix organization and managing by influence.
â?¢ Previous managerial experience in a similar industrial position preferred.
â?¢ Demonstrated ability to forge academic and commercial collaborations is a strong plus. |
| Biogen Idec, Inc. |
Wellesley |
MA |
11/20/2009
|
| Director, Commercial Services, Customer and Partner Services |
| Healthcare industry professional with 10 years of overall experience and 5+ years specific experience leading analytical and contract management programs. Healthcare, pharmaceutical or biotechnology industry related experience preferred. Well developed computer and desktop management skills. Ability to lead in a fast paced, multi-task environment with responsibilities that are diverse. Candidate must have excellent communication, interpersonal and organizational skills. Ability to budget effectively and monitor compliance with budget. |
| Biogen Idec, Inc. |
Waltham |
MA |
11/20/2009
|
| Associate Scientist, Molecular/Cell Biology and Assay Support |
A minimum of 2-3 years of relevant experience. Excellent communication skills are essential and the individual should possess the ability to work well within a team environment.
Job title shall be commensurate with experience |
| Biogen Idec, Inc. |
San Diego |
CA |
11/20/2009
|
| Associate Scientist II, Molecular Discovery |
1 to 5 years laboratory experience.
A solid understanding of the fundamentals/theory of chromatography.
Excellent written and oral communication skills.
Good computer skills.
Experience with FPLC and/or preparative HPLC a plus. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Assoc Director, Investor Relations |
| Position requires a minimum of 8 years experience, preferably in a publicly held healthcare company or as a sell-side analyst. Candidate will have ability to interface effectively at all levels, both internally and externally. Excellent personal communication skills and experience in delivering communications in written, web and other mediums. Position requires 25% travel. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Associate Director, CMC - Early Stage Small Molecule |
| A Ph.D. in Chemistry with 7 + years of experience in the pharmaceutical industry in areas related to CMC. Prior experience in leading CMC teams is essential. Strong communication skills and the ability to work in a matrix environment are essentail elements for this job. |
| Biogen Idec, Inc. |
Wellesley |
MA |
11/20/2009
|
| Manager, Regional Meeting Planning |
â?¢ Leadership skills highly important: must be able to delegate, deliver feedback, and make quick, effective decisions
â?¢ Interpersonal skills highly important: must be able to motivate team, listen to team ideas, and â??readâ? people
â?¢ Communication skills: must be able to communicate with all types of personalities
â?¢ Meeting planning, event planning experience
â?¢ Must have excellent customer service skills
â?¢ Professional experience for at least 10 years
â?¢ 2-3 years of managment experience preferred |
| Biogen Idec, Inc. |
Waltham |
MA |
11/20/2009
|
| Clinical Trial Manager |
â?¢Typically requires at least 5+ years of global drug development with experience managing clinical projects within time, budget, and quality expectations.
â?¢Experience in hematology/oncology clinical research and development very desirable, especially in the areas of hemophilia and clotting disorders.
â?¢NDA/BLA or MAA experience desirable, particularly within an orphan/rare disease therapeutic area.
â?¢Thorough knowledge of GCP, ICH guidelines and awareness of global regulatory requirements/differences for clinical development.
â?¢Detail and process oriented, with excellent project management skills, including risk assessment and contingency planning.
â?¢Demonstrated leadership, communication, and organizational skills, along with problem solving, conflict resolution, and team building skills.
â?¢Proven excellence in cross-functional matrix and/or cross-cultural partnership setting preferred. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Scientist II, Bioanalytical |
| A Ph.D. in cell biology/molecular biology/immunology with 5-7 years of industry experience in a related field is required. Experience in immunoassay development, cell based assay development using a variety of technologies such as ELISA, Biacore, flow cytometry, reporter gene assays, statistical analysis of data is required. Familiarity with PK/PD concepts, and experience in supporting pre-clinical and clinical studies, interaction with pharmacokinetics scientists, toxicologists, clinicians and with regulatory authorities is desirable. Familiarity with GLP compliance procedures and guidelines is a must. |
| Biogen Idec, Inc. |
Sacramento |
CA |
11/20/2009
|
| Area Business Manager, Neurology - Sacramento CA |
| Minimum 5+ years pharmaceutical sales or biotech sales experience required. Experience with reimbursement issues, product launch, and injectable/infusion product selling experience desired. |
| Biogen Idec, Inc. |
Bronx / Upper Manhattan |
NY |
11/20/2009
|
| Area Business Manager, Neurology - Bronx / Upper Manhattan |
| Minimum 5+ years pharmaceutical sales or biotech sales experience required. Experience with reimbursement issues, product launch, and injectable/infusion product selling experience desired. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Principal Scientist, Bioanalytical Chem |
PhD in a science major such as Chemistry and Biochemistry
· >8 years experience in pharmaceutical industry or contract research organization
· Experience in managing/conducting high throughput LC/MS/MS bioanalytical studies to support discovery small molecule projects.
· Excellent organizational, interpersonal and communication skills.
· Solid experience in people and performance management.
· Demonstrated record of scientific publications. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| VP, Regulatory Affairs Syntonix |
Deep functional knowledge and significant experience leading broad range of Regulatory activities with global scope:
â?¢Interfacing with relevant regulatory authorities through all stages of drug development. International Regulatory experience strongly preferred.
â?¢Preparation of major regulatory submissions and supportive amendments or supplements from IND through BLA. Experience with post-marketing commitments and commercial labeling and promotion preferred.
â?¢Direct experience with Orphan Drug, Fast-Track, Priority Review and Accelerated Approval.
â?¢Broad knowledge of international GCP and GMP requirements and the ability to translate market-to-market differences into integrated development approach.
â?¢Assessment of CMC changes, developing comparability protocols based on critical product quality attributes, and translation to clinical planning.
â?¢Good knowledge of evolving RoW Guidelines and Regulations and how to incorporate into global development plans. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Lead, Manufacturing - Dispensary |
Understands the theory and concepts behind biopharmaceutical technology and processes. A strong knowledge of at least one mfg. department with a general understanding of process impact on other mfg. Areas.
Demonstrates ability to recognize deviations from procedures and/or production records. Understanding of in-process specs and limits. Ability to perform validation runs independently. Must possess ability to balance outside projects with production schedule. Understands impact of validation on production.
***Must be able to work rotating shifts - 7:00am/pm to 7:00pm/am***
Education:
BS degree and minimum 6 years of manufacturing experience in a biotech setting.
Appropriate leadership and process experience may be substituted for degree. |
| Biogen Idec, Inc. |
Houston |
TX |
11/20/2009
|
| Area Business Manager, Neurology - Houston TX |
| Minimum 5+ years pharmaceutical sales or biotech sales experience required. Experience with reimbursement issues, product launch, and injectable/infusion product selling experience desired. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Audit Project Manager |
â?¢At least 7-10 years of progressive business experience
â?¢3 to 5 years diversified US and/or International auditing experience, preferably a combination of Big 4 and Lifescience Industry experience.
â?¢Ability to manage short-term projects and entry-level professional staff.
â?¢Detail and deadline oriented
â?¢Excellent analytical, written communications, interpersonal, organizational and presentation skills.
â?¢Ability to travel (15-20%) and work in domestic and international markets for multi-week assignments as necessary. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| (API) Assoc Director, NA Strategic Procurement |
| ? Science /Business degree
? Member of Institute of Procurement
? Very Strong communication and influencing capabilities
? Strong and creative IT skills; must have advanced Presentation Skills and MS Project or similar
? Experience in Supply Chain / Purchasing
? Generic/Pharma experience
? Knowledge of best practice within Supply Chain and Purchasing |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| AD/Dir. Brand Managed Markets - Psychiatry |
| ? Undergraduate degree required; MBA preferred
? Minimum of 5 years Commercial Operations experience including experience in field sales, brand marketing and account management. Experience in market access, pricing & contracting and government affairs and interacting with government and payers is highly desired.
? Demonstrated leadership abilities. Experience as a first line manager of a team preferred.
? Strong entrepreneurial spirit and willingness to take risks
? Exceptional at interpreting and drawing business insights from customer interactions, supported by data and analysis
? Strong at managing bottom line and making financial trade-offs
? Strong understanding of the pharmaceutical industry, payers, providers and external factors impacting the market
______________________________________________________________________________
SKILLS & COMPETENCIES:
? Demonstrated ability to champion a concept from idea to completed program while swiftly navigating the appropriate and necessary approval processes of a large organization
? Ability to deal with ambiguity while achieving clarity in process and capabilities to deliver results
? Deep understanding of the pharmaceutical marketplace and the broad range of customers who impact pharmaceutical market access
? Deep understanding of the government payer system for pharmaceutical products
? Competencies in the following areas: cross-functional leadership, negotiations skills, communication skills (verbal, written & presentation skills), business acumen, strategic marketing, , ability to manage financial resources, analytic skills and decision making
? Demonstrated ability to be a problem solver who can design the strategy and also take it to successful execution |
| Novartis Oncology |
na |
GA |
11/20/2009
|
| Adverse Event Specialist |
| MINIMUM EDUCATION REQUIRED - BS in health-science related field, or a combination of education, experience and technical certifications determined to be equivalent.
MINIMUM EXPERIENCE REQUIRED - Minimum 3 years experience in medical device or related industry with emphasis on product safety. Familiar with global regulations regarding medical devices. Data entry experience required. Prefer experience in audit/compliance, training, quality assessment or an ASQ certification. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Analyst III, Pricing |
| EDUCATION/EXPERIENCE:
BS/BA and 5 years of professional related experience. |
| Novartis Oncology |
na |
NC |
11/20/2009
|
| Analyst, LIMS Technical Support |
| Education/Experience:
High School Diploma and 2 years of related experience. |
| Novartis Oncology |
na |
CO |
11/20/2009
|
| Analytical Research Scientist |
| BS Degree and 3-7 years experience.
Masters Degree and 3 - 4 years experience.
PhD - 1 to 3 years experience.
Previous method development experience required.
Knowledge of cGMPs.
Pharmaceutical industry experience preferred. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Area Scientific Assoc Director MSL, New England (QKQE1K) |
| 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 |
CA |
11/20/2009
|
| Asc Dir Quality Assurance-CMO (Emeryville, Calif) |
| -Bachelor or higher in Biochemistry, Chemistry, Microbiology or another related science
-Fluent in speaking / writing in English
-10 or more years experience in the pharmaceutical industry, with direct experience with Biopharmaceutical APIs. Experience in QA Operations, production, QC and/or other relevant operational areas, but must include minimally 5 years in QA, and 3 years of management and or project management experience. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Asc Dir, Prin Clin Outsourcing |
| Bachelor?s Degree
1. At least 5 years experience in Drug Development in Pharmaceutical Industry or with a CRO/Central Lab/Specialty Provider.
2. Basic understanding of the clinical development process and the management of clinical trials.
3. Demonstrated ability of completing projects on time and within budget.
4. Excellent influencing and negotiation skills.
5. Basic understanding of contracts (including basic legal understanding of terms and conditions).
6. Familiar with the CRO/Central Labs./Specialty Provider marketplace.
7. Good financial understanding (understanding of cost drivers for clinical trials) as it relates to contracts and cost reductions.
8. Excellent written and oral communications skills.
9. Strong problem solving skills.
10. Demonstrated willingness to make decisions and to take responsibility for such.
11. Excellent interpersonal skills (team player). |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Asc Dir/ Dir New Product Strategies |
| A combination of science/marketing-business degrees; advanced degrees preferred; Minimum of 8 years of Pharma industry experience is required that include sales, medical science liaison and/or product management. At least 4 years of oncology experience and knowledge of US market. The candidate must possess strong interpersonal, communication and analytical/strategic thinking abilities. 25% travel is a requirement of this position. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Asc Director Biostatistics |
| PhD in statistics with 5 years of pharmaceutical experience. Strong statistical and data analysis skills; strong knowledge of statistical and clinical trial methodology. Solid hands-on experience as statistician in clinical development program. Good knowledge of drug development process. Experience in supporting NDA submissions. Strong ability in protocol development, analyses and clinical trial reports/publications of Phase I-III clinical trials. Very good oral and written communication skills. Knowledge of FDA/ICH guidelines. Good knowledge of SAS, S-Plus and R computer packages. Good project management skills. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Asc Director Biostatistics |
| Education (minimum/desirable):
PhD or Masters Degree (or equivalent degree) in Statistics, Data mining, Bioinformatics or related field with 3 years or 5 years of experience respectively for senior role.
Languages: Fluent English (oral and written).
Experience/Professional requirement:
? Proven knowledge and expertise in statistics, data mining and/or bioinformatics and their applications to clinical trials. Experience with a wide range of advanced statistical methods. Strong analytical capabilities and data exploration skills.
? Experience in main tasks of a program statistician and as a team leader.
? Proven knowledge of drug development.
? Background knowledge and strong interest in life sciences.
? Proven knowledge of general statistical software packages (e.g. SAS, R/Splus/MATLAB). Knowledge of specialized statistical/data mining tools.
? Good communication, presentation and consultancy skills.
? Creative mind with good problem solving skills. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Asc.Dir/Director Health Economics & Outcomes Research US EBM - CVM |
| The position will be filled at a level commensurate with experience and will require all of the following:
? Undergraduate degree in a relevant scientific/clinical discipline.
? Graduate degree in a relevant discipline focused on health economics and outcomes research methods.
? Minimum 5 years conducting health economics and outcomes research studies related to pharmaceutical products.
? Experience conducting research directly with managed care organizations.
? Strong knowledge of outcomes research methods, including study design and analysis methods.
? Excellent oral and written skills, as well as established background in developing research collaborations.
? Substantial understanding and experience working within the U.S. health care system.
? Understand the role of evidence-based medicine for health policy decision-making.
? Ability to work well in a team environment, as well as independently with limited supervision. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| ASSISTANT BRAND MANAGER 2010 |
| This opportunity is limited to current 2nd year MBA students only.
? Demonstrative strategic and creative problem solving skills
? Strong analytical and leadership skills particularly of cross-functional teams
? Excellent oral and written skills and proactive self-starter.
? Broad understanding of brand management principles. Knowledge of sales and marketing principles and awareness of market research methods
? Computer efficiency required (Word, Excel, PowerPoint, Lotus notes preferred).
? Ability to analyze and summarize marketplace dynamics.
? Internship with consumer packaged goods company or prior marketing experience a plus |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Assoc Dir, Clinical Research |
| Education:
MD, PhD, or PharmD degree
Experience:
3 to 5 years experience in a major pharmaceutical clinical research organization or a CRO |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Assoc Dir/Director Compliance Auditing (Ethics and Compliance) |
| This position will be filed at level commensurate with background of applicant.
Bachelor?s degree in accounting or MBA, Professional certifications (CPA, CFE and CIA certifications) preferred. At least 7 to 9 years broad public or internal audit experience at a major global firm or corporation and expertise in performing and managing compliance, financial, operational and information technology audits and fraud investigations. At least two years of pharmaceutical compliance field sales auditing, prefer three or more of general pharmaceutical compliance auditing. Candidate must possess excellent written and oral skills. Prefer some experience in a leadership capacity. Ability to assess the impact of compliance requirements on the current business environment. The individual must display both a personal and professional maturity that will enable them to remain calm in tense interpersonal situations. The ability to establish and maintain credibility within the organization is imperative. This position demands an individual who is able to protect confidential information and remain discreet in all interactions. This person must be a person of strong conviction who is able and willing to take a difficult or unpopular position when necessary. Ability to travel (up to 25%). |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Assoc Dir/Director Regulatory Compliance (Ethics and Compliance) |
| Requires a BA. Must have 5 to 10 years of specific direct experience interviewing witnesses and investigating cases. JD a plus. Experience in a prosecutor?s office or other law enforcement agency preferred.
KNOWLEDGE AND SKILL REQUIREMENTS:
1. Knowledge of investigative case techniques including document & witness analysis and interviewing skills.
2. Ability to analyze documents, witness statements, case law and provide recommendations. Detailed knowledge of rules of evidence, admissibility of confessions/statements of witnesses; this is normally acquired through a combination of, or, the completion of a Bachelor's Degree and Juris Doctor from an accredited law school or five to ten years of investigative or legal experience.
3. Strong interpersonal and communication 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. Good telephone skills including the ability to conduct interviews by phone. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| 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 |
11/20/2009
|
| Assoc Director, FDF Strategic Procurement |
| Education/Experience:
? Science /Business degree
? Member of Institute of Procurement
? Very Strong communication and influencing capabilities
? Strong and creative IT skills; must have advanced Presentation Skills and MS Project or similar
? Experience in 3rd party relationships
? Generic/Pharma experience
? Knowledge of best practice within Supply Chain and Purchasing |
| Novartis Oncology |
na |
CA |
11/20/2009
|
| Assoc Director/Mgr Sys Support - SF Bay Area |
| ? A minimum of a Bachelors degree in Computer Science, Information Systems or a related discipline with an advance degree preferred.
? A minimum of 12 years industry work experience is required.
? A minimum of 8 years previous management experience in the pharmaceutical industry is required.
? Good business systems knowledge and an understanding of the Company?s computer operating system(s) and application systems required
? Demonstrated experience assessing end-user issues and requirements, demonstrating the ability to resolve and integrate solutions
? Demonstrate knowledge of business analysis and have the ability to understand and evaluate organization wide impacts of application changes
? Experience working in a GMP/GLP pharmaceutical manufacturing environment or other regulated environment
? Must have experience with network systems administration duties (Cisco switches, IP networking, firewalls, DNS, VLANs etc.)
? Strong verbal and written communication skills are required.
? Must be goal-oriented, quality-conscientious, and customer-focused.
? Good laboratory compliance and safety practices are a must.
? Project management skills are required. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Assoc General Counsel |
| Education : Requires J.D.
Experience: Five to ten years experience in a business-oriented law firm, corporate legal organization, governmental agency or equivalent. Substantial expertise representing corporate entities in transactional matters, such as licensing agreements, acquisitions, divestitures, joint ventures, and complex and routine commercial agreements. Other corporate and/or pharmaceuticals legal expertise desirable. Experience reviewing pharmaceutical or related promotional/advertising materials is a plus. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Assoc Medical Dir/Medical Director US AB-GEM (Arthritis) |
| MD, PhD, PharmD or equivalent (MD and rheumatology as a specialty preferred), with a minimum of 3 years experience in US Medical Affairs and Clinical Trial conduct. Knowledge of present and future trends in arthritis and immunology? scientific, research, regulatory, commercial. Good interpersonal and leadership skills. Good communication, presentation and writing skills. Understanding of medical/marketing principles and strategies. Understanding of drug development process. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| ASSOCIATE BRAND MANAGER |
| ? Bachelors degree; MBA preferred
? 1-3 years total brand experience. Consumer Package Goods experience preferred
? Experience in working with and managing agencies, media planning, developing future brand plans, managing budgets, conducting business and market place analysis and developing creative briefs.
? Demonstrative strategic and creative problem solving skills, strong analytical skills, leadership skills particularly of cross-functional teams, oral and written skills and proactive self-starter.
? Broad understanding of brand management principles
? Knowledge of sales and marketing techniques, market research data sources and applications is required
? Outstanding interpersonal skills, with emphasis on ability to influence others in all functions and at all levels in the organization.
? Well-developed oral, written, and analytical skills
? Proficient with Word, Excel, PowerPoint, Lotus Notes |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Associate Director eMarketing |
| ? 3-5 years experience working with interactive marketing tactics is required
? Experience in successfully developing e-marketing plans that have produced positive ROI
? Individual must be able to communicate effectively, present business plans and business updates to high level executives, manage project teams, and balance multiple priorities simultaneously
? Strategic thinker, results oriented, collaborative, energetic, self-directed and motivated
? Demonstrated collaborative skills
? A strong ability to multi-task and the judgment to balance competing priorities effectively
? BA/BS is required. Preference for advanced degree |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Associate Director of Research Management, Program Office |
| ? Master?s or Ph.D. in scientific discipline, project management certification strongly preferred.
? 5+ years experience of working in a project management role within drug discovery in pharma or biotech.
? Will have operated within review committees and have experience of managing within matrix organizations.
? The successful candidate will have proven ability to mentor project management teams and the larger research organization.
? Experience with project management and data collection methodologies and tools essential.
? Experience in facilitation and design of curriculum for project management. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Associate Director, Aggregate Spend/State Law (Ethics & Compliance) |
| ? Bachelor?s Degree in technology or business related field.
? 5 - 10 years of responsibility in business processes, data management, business analysis, or project management capacity.
? Candidate must have a strong detail orientation and focus on quality work product due to the complex and sensitive need for data integrity.
? Candidate should be able to demonstrate solid knowledge of technology solutions and systems.
? Strong communication (written and verbal) and presentation skills required; Ability to interact with multiple cross functional teams at all management levels (IT, sales force compliance, meeting solutions, etc).
? Possess an understanding of business processes and ability to understand end to end processes.
? Must be able to meet project deadlines.
? Excellent organization and database skills are required.
? Demonstrate flexibility and willingness to approach and take on new tasks.
? Candidate must be able to understand and be responsible for appropriate management of sensitive, private, confidential, compliance data. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Associate Director, Medical Strategy-US Biologics |
| ? Minimum of 5 years of industry experience
? Understanding of clinical development pathways and FDA
? Doctorate Degree (PharmD, MD, DO, PhD )required
? Individual must be willing to travel 25% of the time including international travel
? Ability to demonstrate good business judgment
? Position will be located in Princeton, NJ
? Strong analytical, conceptual and administrative skills.
? Exceptional communication skills both oral and written as a need to deliver comprehensive presentations to small/large groups of health care providers and internal management
? Flexibility in adapting/reacting to changing market dynamics and competitive challenges.
? Teamwork is a mandatory requirement as it involves internal/external networking in the district, region, and across the commercial franchise.
? Excellent planning and organizational skills to demonstrate leadership and initiative.
? High sense of urgency and commitment to excellence in the successful achievement of objectives. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Associate Director, Patient Reported Outcomes(PRO) |
| ? Undergraduate degree in a relevant scientific/clinical discipline plus graduate degree (Masters or PhD) in relevant discipline including psychology, health economics, epidemiology, health services research, biostatistics, or public health.
? Minimum of 5 years of direct experience conducting PRO related research for pharmaceutical products.
? Demonstrated leadership experience and accomplishment and/or skill set necessary to manage in a cross functional team environment.
? Prior history of responsibility for development and execution of PRO strategy of products; experience managing products in all phases of development.
? Expert level knowledge in PRO analytical methods; thorough understanding of study designs that provide most relevant evidence to decision-makers; good knowledge of the regulatory and reimbursement environment.
? Familiarity with the regulatory guidelines and established best practices relating to PROs.
? Demonstrated research accomplishments including publications and presentations at scientific conferences.
? Good understanding/awareness of sources of clinical information including disease epidemiology and treatment.
? Thorough understanding of organizational processes, including significant experience working cross-functionally with Clinical Research, Marketing, Pricing, Market Access, and other functional areas.
? Established relationships with PRO thought-leaders. |
| Novartis Oncology |
na |
IL |
11/20/2009
|
| Associate Director, Regional Business Strategy - Chicago |
| ? Undergraduate degree required (M.Sc./MBA preferred)
? Demonstrated competencies and experience in developing business strategies and competitive intelligence; preferably with experience in finance, strategic plan-ning, business development, marketing or consulting
? Superior analytical and financial acumen
? Minimum 5 years pharmaceutical experience, preferably with multi-functional ex-perience and proven performance in those positions
? Ability to communicate effectively across functions, specifically with senior man-agement and HQ functions (e.g. Finance, Strategic Planning, Marketing)
? Self-starter
Skills & Competencies:
? Demonstrates strong competencies in finance, strategic planning, business analysis to uncover opportunities and growth drivers (Competent)
? Analytical Skills: Synthesizes various information sources to draw conclusions and drive actionable recommendations (Competent)
? Consulting Skills: Organizational success achieved through identifying and satis-fying customers? needs, proactively performing value added analyses and provid-ing appropriate support for implementation of required changes (Competent)
? Thinks ?out of the box? and develops innovative solutions to new & existing prob-lems focusing on results (Innovative & Creative)
? Takes on difficult/challenging but achievable goals, identifying gaps & seeks to overcome them (Empowerment/Accountability)
? A ?change agent? who is passionate, high energy results oriented with a creative mind (Results Driven)
? Strong cross-functional perspective ability to establish key relationships and en-sure close alignment with regional leadership team and HQ functions (Collabora-tion)
? Ability to work in situations of ambiguity (Leadership) |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Associate Director, Segment and Pricing Strategy, Oncology |
| - Requirements for the position include leadership, proven results, innovation and application of consistent analytics and data management for designing & evaluating pricing strategies, ensuring compliance with all audit responsibilities. Strong collaboration across US and Global Oncology Brands, Sci Ops, Business Analysis, Finance, Policy and Managed Markets Finance
- Bachelors Degree in Math, Economics or other critical thinking major; advanced business degree (MBA) preferred
- 5+ years experience in the US pharmaceutical industry with an emphasis in pricing or strategic/product functions with a minimum of 5 years in pricing and strategy.
- Strong MS Excel skills including experience in developing financial models.
- Understanding of drug pricing, including First Databank and or Medispan data sources. Knowledge of AMP & ASP pricing including Best Price.
- Knowledge of Business of Oncology, Payer Landscape, and Segment stakeholders.
- Understand and utilize economic, and financial, data to accurately diagnose, analyze and act upon business opportunities.
- Understanding of Benefit Design & Economics associated with Commercial, Medicaid and Medicare Reimbursement for both oral and IV Oncology Pharmaceuticals with Oncology Customers.
- Ability to succinctly and clearly communicate recommended modeling results to leadership team. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Associate II, Regulatory Affairs |
| Education/Experience:
Candidate must possess a Bachelor?s degree or foreign academic equiv. in Pharmaceutical Sciences or directly related field and 5 years experience in pharmaceutical industry. Must have extensive experience in the FDA regulatory submissions and experience in pharmaceutical industry that enables one to evaluate CMC documents that are intended for regulatory review. Experience in drug therapeutic areas (dispensing) that enables one to write/prepare FDA labeling submissions and knowledge of pharmacology that enables one to perform clinical study reports review effectively in this position. Electronic filing experience is highly preferred. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Associate III,Regulatory Affairs |
| Education/Experience:
Minimum requirements BS/BA or higher and 3 years of professional, related work experience |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Associate IV,Regulatory Affairs |
| Education/Experience:
BS/BA or higher and 6 years of professional, related work experience. Electronic filing experience is highly preferred. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Bioinformatics - Oncology Translational Science |
| The ideal candidate will have an MS or higher in computational biology or a related field, with a minimum of 3-5 years research experience. A strong understanding of the application of statistics to biological problems, and experience in the analysis of genomic data, are required. Strong communication skills and a proven track record of interacting with scientific teams are also required. The candidate should be a strong scientific programmer, and ideally will be proficient in Perl and the R statistical language. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Bioinformatics, BMD Expert |
| Minimum requirements The successful candidate will have a Ph.D. in bioinformatics, engineering, physics, statistics, applied mathematics, or a related field with a strong computational background. The candidate should have experience (2+ years) analyzing genome-scale data sets and a working knowledge of molecular biology. Fluency in at least one statistical package (R/Bioconductor preferred) and one programming or scripting language (e.g. Perl, Ruby, Java, Python) is a must, as is experience in a Unix/Linux environment. Familiarity with software packages such as Partek, GeneSpring, GeneData Analyst, and Matlab is also required. Experience with relational databases and SQL is a plus. The successful candidate will be a team player with good communications skills, capable of discussing complex computational concepts with scientists from a variety of backgrounds.
Required years of experience One - Three Years
Education Doctorate Degree |
| Novartis Oncology |
na |
CA |
11/20/2009
|
| Biopharmaceutical Graduate Program - Vacaville, Calif |
| ?Recent MS or Ph.D. program graduate in the life sciences.
?Proven success and demonstrated leadership ability within a previous academic
and/or industrial setting.
?Familiar with the biotech industry, its science and its engineering.
?Must have an awareness of multidimensional/ multivariable differentiation concept and presentation.
?Must be available for worldwide assignment.
?Must have strong interpersonal and communication skills.
?Must be able to multitask effectivel between multiple projects.
?Must be fluent in English and knowledge of German or French would be a plus. |
| Novartis Oncology |
na |
CA |
11/20/2009
|
| Biopharmaceutical Mfg Microbial Fermentation Expert - Vacaville, CA |
| -PhD in Microbiology, Biochemistry, Biochemical/Chemical Engineering
-English required; German or French desirable
-Minimum of 5 years in a commercial manufacturing environment |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Biostatistics Group Head Shanghai China |
| ? At least 8 years of work experience in statistics in clinical development with Ph.D. degree (or equivalent degree/knowledge/expertise) in statistics, mathematics or a closely related field.
? At least 2 years of people management experience in a pharmaceutical company or CRO.
? Strong statistical expertise with focus on its application in clinical trials.
? Excellent communication skills, including in English (written and spoken).
? Good knowledge / understanding of regulatory requirements relevant to statistics (e.g. GCP, ICH, local regulations in China).
? Ability to effectively guide and supervise a group in a complex global team environment. Prior experience in a multinational company or work/college experience abroad is desirable.
Excellent communication skills, including in both English and Chinese (written and spoken).
Work Location: Shanghai, China |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Brand Manager-NoDoz |
| ? Must have 3-5 years consumer package goods brand marketing experience
? Rx marketing experience preferred
? College degree required, MBA preferred
? Broad knowledge of Brand Management, sales and marketing techniques, market research data sources and applications.
? Strong oral, written and presentation skills
? Computer efficiency required (Word, Excel, PowerPoint) |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Brand Safety Leader(CVM MD) |
| Education (minimum/desirable): Medical degree required, Specialty Board certification desirable. Useful additional degrees: Post graduate degree in Pharmaceutical Medicine; Master of Public Health in Epidemiology (or equivalent)
Languages: Fluent in spoken and written English,
Understanding in another language (e.g. French, German, Spanish) desirable.
3 years clinical experience postdoctoral
? At least 5 years are in drug development in a major pharmaceutical company (of which 2 years in a global position), including 2 years in safety at an operational or medical position-
? Experience in preparing or contributing to preparation of clinical safety assessments and regulatory re-ports/submissions involving safety information.
? Experience in leading cross-functional, multi-cultural teams
? Experience with (safety or others) issue management
? Experience in drug development, clinical trial methodology, regulatory requirements, scientific methodology, statistics and writing of publications |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| BS/MS Research Associate: Oncology Cell Biologist |
| The ideal candidate will have either a Bachelors or Masters degree in cellular/molecular biology with at least 2-4 years of experience in biomedical research. Proficiency in standard cellular and molecular biology techniques, including cell culture, cloning, RT-qPCR, immunoblotting, viral production, flow cytometry, and RNAi as well as data analysis/interpretation is critical. The candidate should be highly collaborative, self-motivated, team-oriented, and have excellent communication skills. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| BS/MS Associate: In Vivo Pharmacology Oncology Translational Medicine |
| B.S./M.S. degree in Pharmacology, Molecular Biology, Biochemistry, or equivalent with 2-4 years of experience in animal models of human diseases, preferably in industrial oncology drug discovery. Practice in handling and dosing of rodents and formulation of test compounds is critical. A very strong background in molecular and cell biology with a good knowledge of statistics is essential. Familiarity with Excel, Word, Power Point and graphics applications, as well as excellent writing, communication, and inter-personal skills are very important. The ability to independently prepare drafts of publication-style reports will be a plus. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| BS/MS Associate: Oncology Cell Assay Development |
| The candidate should possess a Bachelors or Masters degree in Molecular and Cellular Biology with at least 2-4 years of relevant experience. Proven hands-on laboratory skills involving robotic equipment and software associated with the equipment, cell assay development, general laboratory automation, high throughput screening, compound management, cell culture techniques, and data analysis/interpretation are a must. Experience with Polara software, high content screening, RNA interference, combination screening are a plus. The candidate should be highly collaborative, self-motivated, team-oriented, and have excellent communication skills. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| BS/MS Associate: Ophthalmology Gene Replacement Therapy |
| The successful candidate will have demonstrated expertise with genetics, molecular and cell biology. Experience in virology and gene therapy, particularly involving the eye, is desirable. Excellent communication skills and ability to work in a team are required. Candidates should have a M.A./M.S. or B.A./B.S. in an appropriate discipline as well as 3 or more years of experience. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| BS/MS Research Associate - Biochemistry Cellular Biology |
| BS/MS degree in cell biology, biochemistry, or molecular biology with 2+ years of relevant research experience is required.
Experience in immunohistochemistry, immunoprecipitation, protein Western blot, protein interaction study, cell culture, and other cell biology/biochemical techniques.
Demonstrated experience with executing experiments, interpreting results, and recording data while functioning independently.
Effective oral and written communication skills.
We are looking for a motivated candidate that works efficiently and collaboratively in a team environment. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| BS/MS Research Associate-Mass Spectrometry |
| Successful candidate will have minimally a BSc degree in the appropriate scientific area, with at least 2-3 years experience of extraction of low molecular weight analytes from plasma and/or tissues and developing LC and/or LC/MS methods to undertake their analysis. Experience with lipids measurement is preferred, but not essential. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| BS/MS Research Associate: Molecular Pharmacology |
| A BS/MS life science degree with proven record of accomplishment and at least 3 years of prior drug discovery experience is required. The candidate must be well organized and able to work independently to plan, execute, interpret and troubleshoot experiments. Strong oral and written communication skills are essential. Excellent time management and multi-tasking skills are required, along with the ability to work collaboratively within a team environment. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| BS/MS Research Associate: Oncology Cell Biologist |
| BS/MS in the sciences with a minimum 5 years of post school experiences preferred. A successful candidate will have demonstrated a high level of competency in hands-on laboratory skills in cell biology, including cell culture, westerns, biochemical enzyme assays, cell based assays including ELISA, RT-PCR, DNA cloning, RNA handling, imaging of cells using microscopes, flow cytometry and various proliferation assays. Must have proficient computer skills in Excel and powerpoint and also should be able to write laboratory reports independently. Candidates from highly reputable biological sciences laboratories in an academic environment as well as those with previous experience in pharmaceutical industry will be considered. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| BSL |
| ? 3 years clinical experience postdoctoral
? At least 7 years of experience in drug development in a major pharmaceutical company, or CRO, or Health Au-thority, including at least 5 years of experience in clinical safety (of which at least 3 years in a global posi-tion)
? Experience in preparing clinical safety assessments, risk/benefit evaluations and regulatory reports
? Experience in leading cross-functional teams
? Experience with safety issue management
? Experience in preparing development documents such as Safety Strategy in Clinical Development Plans, Inves-tigator Brochure
? Knowledge or degree in pharmacokinetics or pharma-cology would be of benefit |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Buyer I |
| EducationExperience:
AS/AA and 3-5 years of professional related experience. Demonstrated proficiency in SAP and Ariba Buyer. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Campus Building Project Leader |
| Education: Undergraduate degree(s) in engineering, architecture, or project /construction management; Masters a plus. 15+ years of program and project management across multiple sites is required.
The successful candidate will have:
?The ability to effectively interact with the company leadership of a major US or European multinational
?A demonstrated history of leading large building design and construction programs through to at least first year of occupancy on time and meeting all major milestones.
?Success in management of very significant investment projects in the pharmaceutical industry.
?Specific experience in designing and constructing lab and animal facilities.
?Well-accepted team player, skilled in managing, organizing and leading international teams.
?Successful history of working with leading first-tier architects.
?Knowledge of, and ability to negotiate and oversee, local project management and construction companies.
?Familiar with local design and construction regulations.
?Proven ability to be able to interact with key industry and government officials and support regular conversations on project status, pending changes in government (local, state) regulations, etc.
?Reputation for the highest personal ethics and standards of business behavior.
?LEED experience with a focus on total cost of ownership.
?Excellent written and oral communication skills in English required. |
| Novartis Oncology |
na |
NC |
11/20/2009
|
| Chemist II, QC |
| EDUCATION/EXPERIENCE:
BS/BA in Chemistry, or life sciences and 3-5 years related experience required. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Clinical Research Manager |
| Four-year university degree (BA/BS). Degree in Life Sciences, Nursing, or equivalent, preferred.
1. Minimum 7 - 10 years experience in drug development for this Clinical Research Manager (CRM) role.
2. Industry experience in a variety of areas with increasing levels of responsibility
3. Knowledge of clinical trial design; basic statistics and pharmacokinetics
4. Solid medical/scientific writing skills; ability to effectively communicate across the business organization, both upward and downward.
5. Knowledge of Oncology therapeutic area strongly preferred. Experience with Solid tumor studies beneficial.
6. Knowledge of good clinical practices (GCP/ICH) and regulatory requirements.
7. Basic working knowledge of clinical database systems.
8. Strong experience and knowledge of basic Microsoft Office computer programs (i.e., word, excel, and project) required. Basic knowledge and experience with Microsoft access a plus.
9. Ability to collaborate and work effectively in teams.
10. Fluency in English (oral and written) required. Conversation ability in other languages a plus.
11. Demonstrates competencies in line with established profile. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Clinical Research Scientist/Sr. CRS |
| 1. Minimum 2 years experience in drug development for CRS role. Clinical trial experience preferred.
2. Basic working knowledge of clinical database systems
3. Knowledge of clinical trial design; basic statistics and pharmacokinetics a plus.
4. Solid medical/scientific writing skills; ability to effectively communicate across the business organization
5. Knowledge of Oncology therapeutic area
6. Knowledge of good clinical practices (GCP/ICH) and regulatory requirements.
7. Ability to collaborate and work effectively in teams.
8. Demonstrates competencies in line with established profile.
9. Ability to manage multiple projects simultaneously.
10. Effectively manage project goals/objectives and timelines.
11.Collaborate with cross functional areas to support project deliverables.
12.Up to 20% travel |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Clinical Trial Budget Manager |
| Bachelor Degree required, preferred in Life Science or Business Administration. Advanced degree preferred (e.g. MBA, MPH, PhD).
1. 2-5 years of pharmaceutical industry experience, with previous experience in either clinical research or finance, in a healthcare environment.
2. Strong financial background.
3. Knowledge of clinical development processes and guidelines.
4. Experience in working with electronic databases, clinical and/or project management planning and reporting systems.
5. Proven effective communication skills.
6. Ability to work on cross-functional global teams. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Clinical Trial Head (Phase 3) |
| Impact on organization:
Responsible for financial/resource decisions within scope of assigned authority.
Well managed and effective trial team(s) resulting in the timely delivery of high quality analysis of clinical trial data which enables strategic decisions within the clinical program.
Education:
Advanced degree or equivalent education/degree in life science/healthcare is strongly recommended. MD, PhD preferred.
Minimal Requirements:
? 5+ years technical, operational and managerial experience in planning, executing, reporting and publishing clinical studies in a pharmaceutical company or contract research organisation.
? Proven ability to work independently, to lead a multidisciplinary trial team in a complex matrix environment (including remote).
? Experience in developing effective relationships with key investigators.
? Thorough knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes, and global clinical development process.
? Advanced knowledge of the Oncology and/or Hematology is preferable. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| CMC Liaison - Pain - Global Regulatory Affairs |
| Education:
- Minimum BA, BS; Preferred MA, MS, PhD, PharmD in Life Science
- Experience:
5+ (Manager) to 8+ (Senior Manager /Associate Director) years in Regulatory Affairs
- Strong successful experience in driving international regulatory activities (Europe, rest of the world) with respect to CMC filing, variations and management of HAs requests - International exposure
- Multicultural skills - strong communicator and customer oriented |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Compliance Paralegal |
| ?Paralegal Certificate plus two year's experience in a corporate law department OR
?Associate's Degree plus five year's experience in a corporate law department
?Must also have experience in the pharmaceutical or medical devices industry
Preferred Requirements:
?Healthcare compliance experience is preferred.
This position also requires professional demeanor, excellent computer skills, judgment in dealing with management, excellent organizational skills, use of utmost discretion in handling confidential information and ability to work with minimal supervision. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Computational ADME Scientist (BS/MS) |
| Candidates possessing an M.Sc. in
Computational Chemistry or a closely related
discipline with 5+ years of experience in in
silico modeling in the drug metabolism and
pharmacokinetics field within a
pharmaceutical or biotechnology company.
An in-depth understanding of all aspects of
computational modeling within DMPK with
special emphasis on descriptor calculation
software, multivariate modeling approaches
and application in the drug discovery setting
is required. A successful candidate must be
able to plan, conduct and interpret ADME
modeling investigations in support of drug
discovery efforts. A good working knowledge
of drug metabolism and pharmacokinetics is
required, with strong competencies in
computational modeling via PLS, RF, neural
networks or similar, as well as descriptor
calculation software. Experience with
pharmacokinetic modeling software (e.g.
WinNonLin), programming language (e.g.
C++, Java), and Linux operating systems is
highly desired. A successful candidate will
need excellent interpersonal skills,
particularly oral and written communication
skills. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Computational Chemistry/Biology Research Investigator (Ph.D) |
| The ideal candidate will possess the following qualifications:
? Ph.D. degree in computational chemistry, computational biology or a related field, with 3+ years of related work experience.
? Familiarity with up-to-date biological screening paradigms.
? A proven track record in leveraging in silico techniques to drive basic science projects or in impacting hit finding activities in a drug discovery environment.
? A solid understanding of chemometrics, which includes QSAR methodologies, data mining and visualization, protein modeling, molecular docking, library design, conformational analysis, pharmacophore development, 2D and 3D similarity.
? A good understanding of bioinformatics and computational biology including gene expression data analysis and mining biological pathways to enhance target knowledge (GeneGO, Ingenuity).
? Demonstrate the ability to work independently as effectively as being able to collaborate in multidisciplinary teams.
? Strong analytical and problem-solving skills and scientific creativity are essential.
? Excellent oral and written communication skills and organizational skills are required.
The following qualifications are a plus:
? A solid experience in a pharmaceutical or biotech environment.
? Background in medicinal chemistry and basic knowledge of synthetic organic chemistry.
? Programming skills in C/C++/C#, Java and scripting in Perl/Python and Pipeline Pilot. |
| Novartis Oncology |
na |
CA |
11/20/2009
|
| Contract Mnfg Consultant (Emeryville, Calif) |
| Degree in related technical field (Biotechnology / Chemical Engineering / (Bio)chemistry) with doctorate (PhD) desirable or appropriate combination of education and experience.
English fluent spoken and written; German & French spoken are a clear ?plus?
Minimal 7-10 years confirmed experience in biotechnology manufacturing, ideally with direct responsibilities in manufacturing operations, 3rd-party management, toll-manufacturing activities or related area; Microbial expression system manufacturing background a plus. |
| Novartis Oncology |
na |
GA |
11/20/2009
|
| Cost Accounting Manager |
| Minimum Education Required: Bachelor?s degree in accounting/finance
Preferred Level: CPA
Minimum Experience Required:8-10 years experience in either inventory or cost analysis, including 2-3 years supervisory experience.
Preferred Level:
? At least 5-8 years in a high transactional environment.
? 5-6 years Cost/Inventory Accounting
? 3-5 years supervising and working with senior management teams
Minimum Skills Required: Intermediate to advanced pc and financial system skills (spreadsheet , database, word processor), interpersonal skills
Preferred Level: Advanced PC skills in Excel and Word plus working knowledge in Access and ERP systems |
| Novartis Oncology |
na |
NC |
11/20/2009
|
| CRM Analyst |
| ? B.S. degree or equivalent technical degree in related area or equivalent related on the job experience
? Expertise in Pivotal 5.9 ( Active Access)
? Strong knowledge of SQL Server and relational database design
? English as primary language, secondary language a plus (Spanish, French or German)
? Minimum of 4 to 6 years experience implementing and supporting Pivotal 5.9 (Active Access )
? Advanced experience with Crystal Reports ( 8 upwards)
? Minimum 2 ? 4 years Visual Basic Version 6
? VB.NET programming experience
? Project management experience (PMP cert. a plus)
? Experience supporting remote sales organization
? Experience writing technical documentation
? Exposure to Pivotal 6.0 |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| CTH / Sr CTH (nonMD) |
| ? ? 6 years technical, operational and managerial experience in planning, executing, reporting and publishing clinical studies in a pharmaceutical company or contract research organisation.
? Experience in multiple clinical indications and/or TAs is preferable.
? Previous experience leading in parallel several trials; leading multidisciplinary trial teams in a complex matrix environment (including remote).
? Demonstrated ability to establish effective working relationships with key investigators.
? Thorough knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes, and global clinical development process.
? Advanced knowledge of the assigned TA is preferred, with the demonstrated capability to interpret, discuss and represent trial or program level data.
? Previous experience in interactions with Health Authorities is preferable.
? Experience in Neuropsychiatric disease areas preferred (i.e. Schizophrenia, bipolar disorder, depression) |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Demand Analyst |
| - 1-2 years of experience as analyst in a large corporation. Previous consumer products and forecasting experience a plus
- The position requires the individual to be exceptionally detail oriented and well organized
- Exposure to SAP APO forecasting module, familiarity with DRP planning systems, IRI and a Business Intelligence (BI) reporting tool
- The individual must have strong analytical, interpersonal and communication skills. Ability to handle and understand large amount of data and communicate demand to various levels of organization
- Expert in MS Excel & Access with ability to build and modify Pivot tables, Access Data bases, Reports
- Strong follow up skills
- Strong time management & multitasking skills
- Bachelors Degree required |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Diagnostics Early Stage Project Team Leader (Breast Cancer) |
| The candidate must possess a PhD in a relevant scientific field, such as Molecular Biology/Genetics, Cancer/Cell Biology, and Biochemistry, with at least 8 years of industrial experience, preferably in the areas of cancer diagnostics.
* In-depth knowledge of disease mechanisms and the relevant signal transduction pathways at the molecular level is essential.
* In-depth knowledge about various technologies for quantification of gene expression and protein detection as cancer diagnostic tools is important.
* Knowledge of and experience in quality and regulatory requirements under which IVD molecular diagnostic products are developed, commercialized and supported (for example 510k or PMA applications, GLP, GCP, and GMP, etc.) are essential.
* Strong management and leadership skills with proven ability to direct and lead project and cross-functional teams effectively in a dynamic environment are required.
* Experience in leading and managing multi-disciplinary R&D projects for IVD applications is highly desirable. Experience in leading and/or managing diagnostic and/or prognostic product development for breast cancer is a plus.
* Excellent communication and presentation skills are essential. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Diagnostics Marketing Director |
| MBA or Equivalent required.
Undergraduate degree in biological
sciences, prior experience in a
molecular diagnostic or life
science tools company with strategy
/ market research focus. Advanced
degree in bioscience an advantage.
Minimum of 10-12 years experience,
with demonstrated ability in broad
range of areas including, but not
limited to marketing; strategic
planning; market research, business
development; financial analysis;
and financial modeling.
Excellent verbal and written
communications, analytical,
organizational and interpersonal
(teamwork oriented) skills
required. Must have strong
presentation skills.
Strong leadership capabilities,
particularly influencing in a
complex matrix organization and
motivating teams across divisions,
cultures and time zones. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Diagnostics Team Leader |
| Education: MS, MD or PhD degree in science discipline
Experience: 5 years development of in vitro molecular diagnostic products, with evidence of products on the market.
Success through FDA/CE/MHLW regulatory process.
Experience managing cross-functional teams and in resource planning.
Experience in Design for Six sigma preferred. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Dir Clinical Rsch Physician, Oncology |
| The successful candidate should have an MD and be Board Certified or board eligible in either hematology or oncology with several years (2 + years) of oncology/hematology clinical research experience in the industry.
Essential requirement will be excellent presentation skills and strong background scientific knowledge base in Hematologic malignancies.
Experience in both Clinical Development and/or Medical Affairs is preferable or a combination of experience in academic medicine with clinical research and/or 1 year of clinical development experience within the pharmaceutical industry.
Experience leading the design, conduct, analysis and reporting of oncology clinical studies is desirable.
Should have demonstrated significant successful interactions with oncology key opinion leaders/investigators.
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.
Ability to work across multiple functions is essential. Effective oral and written communication skills and strong leadership are sought. |
| Novartis Oncology |
na |
CA |
11/20/2009
|
| Dir Quality Assurance - Vacaville, CA |
| -Science degree (MSc or Ph.D. from accredited Technical University) or appropriate education and experience in pharmaceutical industry
-English: fluent in speaking/ writing
-French and/ or German a plus |
| Novartis Oncology |
na |
GA |
11/20/2009
|
| Director ? Key Accounts |
| Education:
? University degree
? Graduate degree in business or finance desirable
Experience/Professional Requirement:
? Extensive (>7 years) sales and sales management experience
? Well-developed record of successful KA relationship management
? Strong negotiation and persuasive ability
? Excellent verbal and presentation skills
? Strong analytical skills
? Excellent People Leadership Skills
? Extensive knowledge of customers? business models
? Strong project management skills
Languages:
? English |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Director of Operations |
| PhD with scientific focus strongly preferred.
Minimum 5-7 years pharmaceutical development experience with exposure to project management/operations and finance coupled with scientific education, PhD preferred. Excellent communication, interpersonal and influencing skills. Broad understanding of drug development and business management. Independent problem-solver with sound judgment, the ability to manage multiple projects simultaneously, implement change and define priorities according to business relevance.
? In-depth understanding of key business processes including in-licensing and external contacts/collaborations
? Interaction at all levels to establish strong communication
? Drive complex projects to completion
? Ability to marshal team forces in forward direction
? Adaptable and flexible yet focused and persistent when necessary
? Excellent presentation skills
? Team oriented individual able to positively influence cross-cultural mem-bers
? Exposure to clinical development or medical affairs preferred |
| Novartis Oncology |
na |
IL |
11/20/2009
|
| Director Regional Strategy & Business Planning |
| ? Undergraduate degree required; MBA preferred
? Minimum 10 years commercial pharmaceutical experience, preferably with multi-functional experience
? Demonstrated cross-functional leadership experience and project management experience a must
? Brand/product marketing experience and thorough understanding of the marketing processes; previous managed markets experience is preferred; thorough knowledge of the integrated healthcare system is preferred
? Demonstrated leadership abilities (experience as second line sales manager preferred) and entrepreneurial spirit
? Exceptional at interpreting and drawing business insights from data and analysis
? Strong at managing bottom line and making financial tradeoffs
? Demonstrated ability to drive complex and innovative cross-functional change
? Ability to communicate effectively with senior executives and across functions
? Strong project & process management skills
Skills & Competencies:
? Excellent leadership & motivational skills, creates an environment which continuously strives to raise performance (Leadership)
? Proven strategic thinking capability demonstrated by examples of implementing strategic to address key issues (Innovative & Creative)
? Thinks ?out of the box? and develops innovative solutions to new & existing problems focusing on results (Innovative & Creative)
? Takes on difficult/challenging but achievable goals, identifying gaps & seeks to overcome them (Empowerment/Accountability)
? A ?change agent? who is passionate, high energy results oriented with a creative mind (Results Driven)
? Ability to work in situations of ambiguity (Leadership)
? Demonstrates competencies in analytics and problem solving to help drive data to uncover opportunities and growth drivers (Competent)
? Ability to work effectively and maintain a strong cross-functional perspective (Col-elaboration)
? Strong cross-functional perspective ability to establish key relationships and en-sure close alignment with regional leadership team and HQ functions (Collaboration) |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Director Strategic Planning |
| M.B.A. and Life Sciences background, strong Pharma consulting experience or Pharma Strategic Planning is necessary.
Minimum of 7 years cumulative experience combined with in-depth biologics industry knowledge a plus. Must have excellent project management skills, e.g. work planning, people management / coaching.
Excellent written and oral English communication skills e.g. writing presentations for top management and presenting to senior management. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Director Translational Med Research Oncology |
| Education:
?MD/PharmD/PhD with revelant experience including previous scientific program leadership
?Must have significant, highly relevant experience in Oncology clinical trial & clinical operations.
Experience:
?Conscientious, enthusiastic team player with excellent interpersonal as well as verbal and written skills.
?Strong leadership skills; ability to effectively work within internal teams across disciplines, with external collaborators and with contract research organizations.
?Must demonstrate good judgment and initiative.
?Must be hands-on, be detail oriented and work well under pressure.
?Demonstrated track records in the ability to effectively influence decisions inside the organization as well as the ability to drive efforts and overcome obstacles. |
| Novartis Oncology |
na |
NC |
11/20/2009
|
| Director-Global Quality Systems |
| ? Bachelor?s degree in Science, Engineering, Math or related field.
? 15+ years experience in regulated industry; 5+ years in leadership role.
? Technical knowledge of various drug manufacturing process
? Experience in Quality Assurance & Quality Systems management.
? in-depth knowledge of chemical/pharmaceutical processes
? In-depth knowledge of regulatory requirements for GMP (Swissmedic, EMEA, FDA) and other international institutions (e.g., VICH, ISPE, PDA
? In-depth knowledge of Computerized System Validation,Standard industry systems e.g., SAP, Trackwise etc. and computer system operation principles |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Director, Customer Marketing Psychiatry |
| ? Undergraduate degree required; MBA preferred
? Minimum 10 years commercial pharmaceutical experience, preferable with mulit-functional experience
? Sales and sales management experience
? Brand/product marketing experience and thorough understanding of the marketing process
? Previous managed markets experience is preferred; thorough knowledge of the integrated healthcare system is preferred
? Previous experience wit the healthcare industry either on the customer side (health plan, institution, retailer, non-profit advocacy group) or at an agency with a client base that contains healthcare customers (non-pharma) preferred
? Demonstrated leadership abilities. Experience as second line Sales Manager and Brand Director preferred.
? Strong entrepreneurial spirit and willingness to take risks
? Exceptional at interpreting and drawing business insights from customer interactions, supported by data and analysis
? Strong at managing bottom line and making financial trade-offs
? Demonstrated ability to drive complex and innovative cross-functional change
? Exceptional understanding of the pharmaceutical industry and external factors impacting the market
Preferred:
? Customer Focus and ability to translate customer interactions into actionable insights
? Results Focus
? Fast, Action Oriented, proactively takes initiative
? Ability to deal with ambiguity while achieving clarity in process and capabilities to deliver results
? Deep understanding of the pharmaceutical marketplace and the broad range of customers who impact pharmaceutical treatment selection
? Exceptional competencies in the following areas: cross-functional leadership, communication skills (verbal, written & presentation skills), business acumen, strategic marketing, inter-dependent partnering skills, ability to manage financial resources, strategic analytic skills and decision making
? Demonstrated ability to be a problem solver who can design the strategy and also take it to successful execution
? Strong track record in driving breakthrough thinking that leads to development of successful business practices and creation of broad based commercial opportunities |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Director, Global Purchasing, Direct Materials |
| Education:
BS degree; MBA, C.P.M preferred
Financial management and reporting preferable
Experience:
10 years in Purchasing preferably in Healthcare/ FMCG envi-ronment
Project Management experience (min 5 years) |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Director, NIBR Communications |
| ? 8-10 years experience in internal, external and crisis management communications,
? Superb oral, written communication and presentation skills
? Flexibility to manage competing priorities and shift focus as determined by changing needs
? Intelligence and poise to work with executives
? Demonstrated record of success in synthesizing issues to develop effective communications
? Excellent organizational skills and ability to consistently meet deadlines
? Experience in establishing and leading well-functioning, engaged, and adaptable team
? Strong leadership skills, creativity, and ability to interact with customers, partners and foster cross-functional teamwork
? Ability to manage multiple, high-detail, deadline-sensitive projects with a high level of quality in all deliverables
? Experience working in a large Biotechnology, Pharmaceutical or Life Sciences corporate environment |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Director, Oncology Business Development & Licensing |
| Required:
? Excellent knowledge of the science, medicine, and business of Oncology (minimum 3 years)
? Strong business acumen combined with experience in structuring, negotiating and successfully closing deals (minimum 3 years)
? Excellent knowledge of the Pharma or Biotech industry, including global drug registration processes (minimum 6 years; Pharma industry experience preferable)
? Working familiarity with Drug Development, Regulatory, Manufacturing, Marketing, Finance, Patents and Legal issues
? Outstanding communication skills
? Strong leadership skills or potential
? High-energy, tenacity and resilience
Desirable:
? Advanced science or medical degree (MD, PhD, or PharmD)
? Master of Business Administration
? English, any other major language |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Director, Strategic Sourcing - Solutions |
| ? University degree or equivalent (e.g. BS or BA) with MBA
? Local Language and English
? 7-10 years in business role with proven cross functional project management
Strong People mgmt experience and experience in a sourcing function
? A proven track record of achievement
? Proven experience in eSourcing, eProcurement and Receive-to-Pay process
? Proven experience in building systems strategy and roadmap
? Experience in company-wide change management and stakeholder management
? Experience in Sourcing Category Management Process for managing suppliers
? Understanding of Financial Management and controls Practices |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| District Manager - 1ZE - Brick, NJ |
| Bachelor's degree (preferably in Life Sciences, Pharmacy, or Business related discipline) 3 or more years of pharmaceutical sales experience At least two years of pharmaceutical sales management experience Preferred Requirements: 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. 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 |
NY |
11/20/2009
|
| District Manager I - 1ZDE - New York City |
| Bachelor's degree (preferably in Life Sciences, Pharmacy, or Business related discipline) 3 or more years of pharmaceutical sales experience At least two years of pharmaceutical sales management experience Preferred Requirements: 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. 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 |
NJ |
11/20/2009
|
| District Manager I - 1ZED - Atlantic City, NJ |
| Bachelor's degree (preferably in Life Sciences, Pharmacy, or Business related discipline) 3 or more years of pharmaceutical sales experience At least two years of pharmaceutical sales management experience Preferred Requirements: 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. 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 |
NY |
11/20/2009
|
| District Sales Manager- New Jersey/New York City |
| Minimum Requirements:
-Four or more years of Sales Management experience in consumer products and or life sciences industries.
-6 or more years front line sales experience in consumer products and or life sciences industries.
-Experience with consultative selling.
-Bachelors degree in Business or related field.
-Strong analytic skills and experience analyzing regions and territories to discover market trend and new opportunities.
-Strong Excel and PowerPoint Skills
-Skills with Customer Relationship Management and Sales Reporting systems.
Required Skills and Experiences:
-Successful candidates will have led regions that have received top sales awards; President?s Club, Circle of Excellence, etc. and consistently be ranked in the top 10% of the selling organization.
-Demonstrated leadership as evidenced by consistently improving sales performance through people development.
-Expert knowledge in the selling process and an ability to coach and develop other?s selling skills.
-Demonstrated success selling product features and benefits rather than selling on price.
-Experience as a District or Regional Sales Manager with 7-10 direct reports.
-Strong customer orientation demonstrated through selling experiences.
-Selling and management experience in business-to-business, pharmaceutical, medical device, and or consumer products. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Executive Administrative Assistant, Ophthalmology |
| A minimum of seven years as an administrative professional supporting executive level management. AS/BS degree required. Proven experience handling confidential and sensitive information is essential. Advanced knowledge of Microsoft Word, PowerPoint, Excel, Lotus Notes (or Outlook) required. Must possess excellent organization skills and have a high attention to detail with a desire to get jobs completed accurately and in a timely manner. Project Management skills are a plus.
Additionally, this candidate will be self-motivated, have excellent interpersonal skills and the ability to build professional relationships. They will also possess the ability to work independently and as an effective and engaged team member in a fast-paced environment. Strong initiative and follow through is essential. Candidates with a proven ability to provide guidance and/or support to Administrative Assistants is a preferred. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Executive Assistant, Global Head Preclinical Safety |
| A minimum of 3-5 years as an administrative professional supporting executive level management. AS/BS degree required. Proven experience handling confidential and sensitive information is essential. Advanced knowledge of Microsoft Word, PowerPoint, Excel, Lotus Notes (or Outlook) required. Must possess excellent organization skills and have a high attention to detail with a desire to get the job completed accurately and in a timely manner. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Executive Director, Global Head of Oncology Development Finance |
| ? University degree in business, economics, finance or related field required
? MBA/advanced degree in business, economics, or finance strongly preferred
? CPA or equivalent beneficial
? English fluency required
? Other languages helpful
? Strong Finance experience required min 10-12 years with Development Finance experience preferred
? Strong analytic skills and experience structuring complex problem solving
? Strong interpersonal and influencing skills
? Excellent team player with demonstrated ability to build collaborative relationships
? Strong verbal and written communication skills.
? Strong project management skills and experience
? Knowledge of Financial systems, (e.g., SAP, TM1, COGNOS, OSS helpful)
? Knowledge of financial controls processes and SOX driven financial policies
? Knowledge of Pharmaceutical Drug Development processes
? Experience working in an international environment helpful |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Executive Director, Quality Assurance |
| minimum required travel 60%required.
Education and training: Graduate in Chemistry, Pharmacy, Microbiology or another related science
Excellent oral and written English communication skills. Second language is preferred.
Minimum 10 years board experience in Pharmaceutical industry or a related regulatory industry. Valid operational experience includes production of QA/QC operations, quality management experience, development or other relevant experience working at a regulatory health authority. Broad business awareness.
Expertise in one or more areas: Facilities, CSV, Laboratory, Aseptic manufacturing, Microbiology, Biopharmaceuticals, Pharmacovigilance, etc.
Expertise in Compliance and health authority interactions. Expertise in GxPs, working knowledge of legal, quality engineering concepts, risk management techniques.
Experience working on teams (multiple roles) and projects. Working knowledge of global regulatory requirements required.
Involvement in Industry forums desired. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Expert Clinical Manager |
| Phase I Oncology clinical trial experience a requirement. On an exception basis highly-qualified candidates with strong oncology experience with Phase 2/3 clinical trial experience might also be considered. Candidates should have 3-5 years of experience in clinical environment (at least 2+ pharma. industry). University degree in Biological Sciences/Nursing/Pharmacy is a minimum. Candidates must demonstrate:
* strong oral and written communications skills and experience in medical scientific writing protocols and Clinical Trial Reports independently
* experience and ability to recognize safety and efficacy data trends independently
* knowledge of clinical trial design, statistics and pharmacokinetics
* experienced with all aspects of the drug development process
* knowledge of medical, scientific and clinical research techniques of the assigned areas
* knowledge of GCP and local regulatory requirements |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Expert Statistician Shanghai China |
| Minimum Requirements
? At least Master?s Degree in statistics or a closely related field.
? At least 7 years of experience in drug development (4 years for Ph.D.).
? Solid knowledge and experience in drug development and Health Authority guidelines.
? Prior experience in dealing with health authorities desired.
? Good command of English, written and spoken.
? Ability to manage projects and supervise other team members
? Work or college experience in another country or demonstrated ability working together in a multicultural organization desired.
? Advanced knowledge of statistical software, in particular SAS. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Facilitators for pharmaceutical teams curriculum |
| Experienced Facilitators with references needed. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Fellow, Endocrine and Reproductive Toxicology (Cambridge) |
| Minimum Requirements
? Ph.D. degree in Biochemistry, Physiology, Cell Biology, Toxicology or a related Biological Science.
? At least 2 years of prior experience in pharmaceutical drug development and/or toxicological sciences is required
? A strong expertise in hormonal disruption and toxicology, and reprotoxicology
? 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, 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 |
MA |
11/20/2009
|
| Fellow/Senior Fellow Safety Genomics |
| Education: MD, DVM or PhD in life sciences.
Extensive operational knowledge of histology and basic pathology.
Basic knowledge of molecular biology techniques and biomedical statistics
Experience: Significant scientific experience working in histology, pathology or molecular pathology
Technical Ability: Experience interpretation of gene expression profiles and integration in the context of a specific apthology/disease
Excellence in data summarization
Presentation: Excellent oral and written communication skills. Able to present and defend data and to influence the decision process regarding study design. |
| Novartis Oncology |
na |
FL |
11/20/2009
|
| General Management/ Leadership roles |
| Experience leading a BU; cross-functional management experience; management of P&L |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| General Management/ Leadership roles |
| Experience leading a BU; cross-functional management experience; management of P&L |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Global Brand Medical Director |
| Education: MD Required
? 10 years of involvement in drug development spanning clinical activities in Phases II/IV or comparable experience in industry.
? 5 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.
? 5 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 organizational 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.
? Demonstrated technical knowledge and innovation in clinical development study designs that provide relevant evidence to decision-makers.
? Prior history with post-marketing/brand optimization studies to obtain evidence of brand value and support commercialization activities preferred. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Global Category Manager - Health Economics & Outcomes Research |
| University (Bachelors) in a scientific field (Preferred) or BS in other field with applicable experience, relevant advanced degree in scientific/clinical experience
Graduate Degree in Business (Preferred)
Certified Purchasing Manager (CPM) or equivalent experience
1. Broad business experience to include purchasing/sourcing in progressive companies where best in class practices are employed.
2. Experience with database sources for health economics and outcomes research, and experience in sourcing pharmacovigilance/medical safety
3. Strong leadership and effective business partnering capabilities.
4. Proven ability to lead cross-functional teams in a complex organization |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Global Category Purchasing Manager |
| ? Bachelors degree
? Minimum 10 years experience in strategic sourcing in a global company
? Strong negotiating skills
? Solid understanding of general business drivers, and concepts
? Six Sigma skills and training desired
? Familiarity with Purchasing systems and tools (ARIBA, Emptoris)
? Project management experience
? Proven people management skills
? Ability to work in a matrix organization
? Excellent written and verbal communication skills
? Fluency in English, any additional languages an asset |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Global Program Diagnostics Director |
| Education: Doctoral in life sciences or chemistry, or MBA with equivalent experience in life sciences.
Languages: Fluent English (written and oral), on other language
Experience/Professional Requirement:
1. 12+ years industry experience
2. 5+ years multi/cross functional leadership experience
3. International drug or diagnostic development project functional leadership
4. Have an advanced understanding of the diagnostic development process and programs.
5. Provide thought-leading insights to the competitive environment and internal partner interfaces
6. Sound knowledge of international customs and business practice
7. Hands on experience with a major submission and regulatory review process
8. Proven people leadership capabilities
9. Model natural leadership characteristics
10. Expert leadership skills demonstrated in GPT, in staff management role or in other organisational assignments. Expert skills to facilitate/optimise contribution of team members as individuals and members of cohesive team.
11. Strong interpersonal and communication skills for bridging scientific and business participants, for negotiating timelines and for effective international collaboration.
12. Outstanding verbal and written communications.
13. Diagnostic or therapeutic experience is an advantage |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Global Program Medical Director |
| ? MD required. Advanced knowledge in medical/scientific area required.
Languages:
Fluent oral and written English
Experience/Professional requirement:
? ? 10 years of involvement in drug development spanning clinical activities in Phases II/IV or comparable experience in industry.
? ? 5 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.
? ? 5 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 organizational 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.
? Demonstrated technical knowledge and innovation in clinical development study designs that provide relevant evidence to decision-makers.
? Prior history with post-marketing/brand optimization studies to obtain evidence of brand value and support commercialization activities preferred. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Global Program Medical Director |
| Education (minimum/desirable):
? MD required. Advanced knowledge in medical/scientific area required - focus is on the Cardiovascular therapeutic area.
Languages:
Fluent oral and written English
Experience/Professional requirement:
? ? 10 years of involvement in drug development spanning clinical activities in Phases II/IV or comparable experience in industry.
? ? 5 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.
? ? 5 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 organizational 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.
? Demonstrated technical knowledge and innovation in clinical development study designs that provide relevant evidence to decision-makers.
? Prior history with post-marketing/brand optimization studies to obtain evidence of brand value and support commercialization activities preferred. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Global Research Operations Information Manager |
| ?5-7 years of experience managing website content and experience using the intranet as a communications/marketing tool
?Experience in creative problem-solving and consensus building in a highly matrixed environment required
?Hands-on experience designing and maintaining large websites including look and feel management within provided guidelines required
?Ability to author web pages using HTML, Java Script, Flash and different tools using these technologies
?Expertise with SharePoint required
?Knowledge of Photoshop, Illustrator, Fireworks and/or other graphical editing tools
?Exposure to large content management systems like Interwoven TeamSite, Documentum, Vignette and familiarity with BEA Weblogic Portal technology or other portal platforms
?Strong interpersonal, relationship, and community building skills are essential
?Some travel may be needed
Education:
?Bachelor?s Degree in Business, Communications or equivalent |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Group Head, Biochemical & Organ Toxicology (Cambridge) |
| We are seeking an experienced scientist and manager to lead a Biochemical & Organ Toxicology group within Investigative Toxicology (Preclinical Safety, Translational Sciences) based in Cambridge, MA. Investigative Toxicology is using non-clinical innovative investigations to discover the mechanisms of target organ toxicity and to prevent and solve pre-clinical and clinical drug safety issues. The candidate will be responsible for the design and set-up of new experimental facilities for 3 laboratories, and the management of staff therein. The candidate will also be responsible for subsequent development, implementation and management of experimental studies. The primary deliverable of these laboratories (Endocrine & Repro-toxicology, Protein & Mitochondrial Toxicology and Biochemical & Cellular Toxicology) will be to facilitate the early identification and characterisation of toxicities during preclinical phases of drug development with a particular focus on Novartis Institute for Biomedical Research (NIBR) disease areas, expertise and technologies in Cambridge. In addition, the candidate will also work closely with Preclinical Safety Project Team Representatives to help assess potential safety liabilities associated with novel drugs and their target(s). The candidate will report to the Global Head of Biochemical and Organ Toxicology and will interact closely with colleagues in other groups as a member of cross-functional and multi-disciplinary teams (including global Investigative Toxicology & Preclinical Safety departments, NIBR and external collaborators). |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Head of Bioinformatics & Biostatistics |
| Education:
Minimum ? MS, Desirable - PhD
Experience: Minimum - 8 years , Desirable ? 10 years.
Management experience: Minimum ? 4 years, Desirable ? 6 years. In vitro diagnostics experience essential.
Specific Professional Competencies:
- Must have proven proficiency in common statistical and data mining techniques used in analyzing biological data.
- Must have experience using R, Matlab, Spotfire, Partek or similar data analysis software.
- Proficiency in developing applications in high-level (Java, C++, C#) and scripting (Perl, Python, Ruby) programming languages to accomplish bioinformatics tasks. Familiarity with web frameworks such as Rails or Django is highly desirable.
- Experience using relational databases such as SQL Server, Oracle or PostgreSQL
- Knowledge of bioinformatics tools and databases such as the NCBI and UCSC Genome Browser, BLAST, Primer3, GEO and BioConductor
- Knowledge of pathway analysis and tools such as Ingenuity Pathway Analysis and GeneGo?s MetaCore is highly desirable.
- Familiarity with assay development and common laboratory techniques is highly desirable.
- Good understanding of molecular biology and diagnostic development is highly desirable.
- Must have excellent communication and presentation skills. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Head of Biostatistics |
| Ph.D. in Statistics or Biostatistics, plus 6-8 years of directly related managerial experience in In vitro diagnostics industry. Demonstrated management and leadership skills. Master the knowledge of statistical theory and applications pertaining to design of experiments, general linear models and variance components. Knowledge and experience in analysis of high dimensional data, especially clustering and classification methods and predictive statistical models for genetics and genomics data. Capable of technically addressing and solving unique statistical problems. Knowledge of appropriate regulatory agency regulations and guidelines. Excellent oral and written communication skills. Strong interpersonal and leadership skills. Ability to provide clear, technically sound, well-communicated guidance to non-statisticians. Self-motivated; ability to work independently and complete work on a timely basis. Skilled SAS programming knowledge; other statistical package knowledge a plus. Pharmaceutical/Biotechnology industry experience in assay validation, quality control, process optimization and validation, design of experiments, and pharmacokinetics. Experience with coordinating/tracking of resources, others? workloads and multiple projects. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Head of Engineering |
| BS/MS (PhD preferred) in
Engineering (Biomedical/
Bioengineering, Mechanical,
Electronic, Chemical, Systems) with
minimum of 7 years experience in
Life sciences or medical device
development.
English
In vitro molecular
diagnostics experience essential.
Familiar with regulatory and
compliance requirements for
diagnostic tests.
Experience in engineering design,
optics,
hardware, system architecture,
application support, and
disposables. Minimum 2 years in
role as systems engineer or system
analyst.
Experience working on multi-
disciplinary projects.
Strong knowledge of assay chemistry
for diagnostic tests/ molecular
biology.
Excellent oral and written
communication skills with the
proven ability to work effectively
across a matrixed and widely
dispersed organization.
Ability to lead and succeed in a
multi-cultural environment. |
| Novartis Oncology |
na |
WA |
11/20/2009
|
| Hematology Sales Representative/Specialist - Spokane, WA |
| 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 |
MA |
11/20/2009
|
| Histotechnology Research Scientist (BS/MS) |
| The ideal candidate will have a BS or MS degree in a biological or chemical science discipline plus at least 4 years of histology experience. Strong organizational skills, self-motivation, attention to detail, flexibility, proactive willingness and desire to engage in the laboratory workflow, and an ability to contribute to a team environment are essential. Candidates should have experience working in a fast-paced, high volume, high productivity and quality environment, in either an industry or clinical laboratory. Experience and proficiency with immunohistochemistry methodology and image analysis is strongly preferred. Prior experience in cell biology and/or molecular biology techniques is preferred. |
| Novartis Oncology |
na |
CA |
11/20/2009
|
| Hospital Sales Representative - Inland Empire, CA |
| Bachelor's Degree (preferably in Life Sciences, Pharmacy or Business related discipline).
? Minimum of 2 years of demonstrated successful pharmaceutical sales experience.
? Ability to work with academic customers.
? Knowledge of relationships between managed care and institutions.
? Exceptional use of time management, planning, organizational and selling skills.
? Experience/ability to quickly learn and master key products and markets in assigned therapeutic area.
? Computer (Word, Excel, PowerPoint) and hand held device literacy preferred.
Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| HR Generalist |
| Education/Experience:
Bachelors Degree required Masters Degree in HR preferred.
1 or 2 Internships in a Human Resources generalist capacity required.
Detail orientated and excellent communication skills, strong experience with Lotus Notes, PowerPoint and Microsoft Office required.
Applicant Tracking System and Peoplesoft experience preferred. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| HR Summer Internship 2010 - Master Level |
| Bachelor's Degree with 1 year towards Masters Degree
? 3-7 years Human Resources experience
? Data management experience; Excel, Access, PowerPoint proficiency
? Strong verbal and written communication skills
? Analytical skills
? Strong project and time-management skills
? Exceptional organizational and time management skills
? Excellent follow-through and attention to detail
? Ability to work independently
? Knowledge of political environment and healthcare policy ? preferred |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| IMS Unit Head -OTM |
| ? 3 years clinical experience postdoctoral
? At least 7 years in drug development in a major pharma-ceutical company (of which 5 years in a global position), including 5 years in safety at an operational or medical po-sition
? Experience in early clinical development/translational medicine and in due diligences
? Experience in preparing of clinical safety assessments and regulatory reports/submissions involving safety informa-tion.
? Experience in leading cross-functional teams.
? Experience in drug development, clinical trial methodology, regulatory requirements, scientific methodology, statistics and writing of publications
? Desirable: Management experience |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Innate Immunity/TLR Biology 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 in the study of innate immunity including inflammasome 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 |
GA |
11/20/2009
|
| Inside Sales Representative |
| Education and Experience:
Bachelor?s degree or equivalent and 2-4 years successful inside or outside sales experience. Some air travel required. Must successfully complete our 4 week ?New Hire Sales Training Program?.
Preferred Experience:
One year contact lens sales/ophthalmic related sales/contact fitting experience.
Bi-lingual (English and Spanish) preferred. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Integrated Information Sciences&Operations(IIS) Global Program Head |
| Minimum: Advanced degree in science or relevant discipline or equivalent
Languages: Excellent English required (oral & written). Good skills in site (local) language desired (oral).
Experience/Professional requirement: Minimum 10+ in drug development and 5-7 years managing teams.
Demonstrated leadership and management skills. Expert skills in managing and directing global multifunctional teams to a shared vision and a common goal.
Drug Development domain expert in clinical trial methodology: planning, execution, and reporting.
Project management proficiency.
Proven track record in working across a matrix organization and demonstrates skills in building partnerships, negotiating agreements; excels at collaboration |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| IT Application Management |
| -BS Degree in Computer Science or equivalent preferred
-6 years or more experience to include service delivery & management of document/records management systems
-Strong Documentum 6.5 (WebTop, BPM, BPI, DTS/CTS)
-Strong Java background
-Strong Web Application background (Tomcat, JBoss)
-Strong ITIL Service Management
-Medium Project Management
-Scientific background preferred |
| Novartis Oncology |
na |
OK |
11/20/2009
|
| Key Account Manager, Swine Southwest US |
| BS/BA or equivalent
? 8-10 years of experience/understanding of livestock production preferred.
? 6 years of swine experience preferred
? Ability to interpret and communicate information from a variety of technical manuals, journals and bulletins.
? Knowledgeable practices of PC package tools, including but not limited to: word-processing (Word), Spreadsheets (Excel) and Presentations (PowerPoint), e-mail (Lotus Notes).
? Valid driver operator license.
? Must reside within the boundaries of the Territory. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Lab Head, Antibody & Protein Design, Novartis Biologics |
| This role requires a PhD in Biochemistry, Molecular Biology or Immunology and a minimum of 3 years of relevant post-doc experience.
Strong team-working focus and excellent communications and inter-personal skills.
Strong proven scientific track record in the discovery and engineering of therapeutic antibodies and proteins.
The role is located in Cambridge, MA and reports to the Unit Head of Protein Design. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Lab Head, Antibody & Protein Structure |
| This role requires a PhD in Biochemistry, Molecular Biology or Structural Biology and a minimum of 2-3 years of relevant post-doc experience in antibody/protein structure study.
A strong team-working focus and excellent communications and inter-personal skills.
A proven scientific track record in the design and engineering of therapeutic antibodies and proteins. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Lab Head, Mammalian Cell Line Development |
| A Ph.D. and postdoctoral fellowship in biology, cell biology, immunology, or related life science field and experience in the biotechnology or pharmaceutical industry are required. Managerial experience is also desirable.
The Lab Head is expected to perform and supervise hands-on laboratory work. A highly collaborative spirit and ability to work on multiple projects is desirable.
Successful candidate will have excellent written and oral communication skills, will be well organized and will thrive in a fast-paced, lean and dynamic organization. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Lab of the Future (LOTF) Project Manager |
| Advanced degree in a scientific (biology or chemistry) discipline. MBA is a plus. Project management proficiency and experience in biotech/pharma required. Excellent communication, presentation and written skills in English are essential; German or Mandarin a plus.
?Generally proficient with design, business, and science concepts in order to better collaborate with scientists, architects, IT professionals, etc.
?Proven ability to set and meet performance targets within a predefined budget and timeline
?Excellent understanding of laboratory environments
?Ability to work collaboratively with and influence multiple stakeholders and users
?Excellent command of Microsoft Office
?Comfort with ambiguity
?Demonstrated ability to innovate
?Results driven
?Highly committed and self-disciplined |
| Novartis Oncology |
na |
NE |
11/20/2009
|
| Lean Sensei |
| Required::
? Bachelor?s degree in science- or engineering-related field. MS or MBA preferred.
? 15+ years of business/operations management or manufacturing experience with management responsibilities.
? Lean expert training, excellent skills using IT applications to organize and analyze data (MS-Access, MS-Excel, Minitab, IGraphX, etc.). Desired: Proficiency in design for manufacturability.
? Hands-on experience with deploying TPS-based lean methods in operations is a critical requirement.
? Technical mastery of continuous improvement tools and methodologies.
? Certified Lean Expert/TPS based.
? Results-oriented, strong analytical skills, and demonstrated process improvement success in managing large teams in a continuous improvement culture.
? Proven change agent and ability to lead teams through: Making case for change; stakeholder management; change communications; removing barriers; setting milestones and acknowledging progress; and reinforcing change through organizational systems.
? Strategic focus.
? Collaborative Leadership: Willingness to work on the shop floor and lead by example; ability to influence decision making with or without authority; facilitate groups with diverse perspectives; and bring teams to agreement. High tolerance for ambiguity.
? Must have strong interpersonal and communication skills that build productive relationships and influences others, both within the business and across organizations.
? Must have a strong track record of collaborating effectively with others in the spirit of common objectives.
? Communication: Ability to interact with all levels of the business (senior leaders to working teams); exceptionally good listening skills; able to present complex or new ideas with clarity and simplicity.
? Planning and Execution: Excellent project management and prioritization skills. Solid business acumen. Able to deliver results despite shifting environment.
? Analytical Problem Solving: Able to identify problems; apply structured and disciplined methodology to identify root cause using data. Innovative and effective solution development, risk mitigation and execution. Hands-on experience with most of the following Lean/problem-solving tools: DMAIC, Lean, voice of the customer, SMART problem and goal statements, SIPOC and process mapping, process capability analysis, failure mode and effects analysis, graphical methods, measurement systems analysis, hypothesis testing, analytical hierarchy process, benchmarking, design of experiments, quality function deployment, control charts, standardized work. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Manager Business Planning |
| ? BS/BA/CPA in Finance or Accounting and MBA strongly preferred
? 3 ? 5 years of directly and progressively responsible experience and demonstrated achievement in financial analysis, with a focus on improving analytical decision making, preferably in the pharmaceutical industry
? Broad understanding of various financial management areas such as financial statement analysis, accounting, budgeting, profitability analysis, costing, consolidated financials
? Excellent knowledge of Excel and Powerpoint with working knowledge of SAP R3, BW, TM1 and Business Warehouse or other data warehousing applications desirable
? Highly motivated self-starter with a willingness to assume responsibility, take ownership for their work and intelligently challenge the status quo
? Possesses a strong sense of urgency to meet deadlines, while maintaining attention to detail and quality of work
? Strong team player than can work effectively in cross-functional teams
? Strong analytical skills with the ability to recognize problems, develop solutions and implement them
? International mindset and ability to work in a multi cultural environment
? Excellent communication skills, both verbally and in writing; ability to relay financial information to non-finance groups and interface with all levels of management |
| Novartis Oncology |
na |
CA |
11/20/2009
|
| Manager Quality Assurance-CMO (Emeryville, Calif) |
| -Bachelor or higher in Biochemistry, Chemistry, Microbiology or another related science
-Fluent in speaking / writing in English
-7 to 10 years experience in the pharmaceutical industry, with direct experience with Biopharmaceutical APIs. Experience in QA Operations, production, QC and/or other relevant operational areas, but must include minimally 5 years in QA, and 3 years of management and or project management experience. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Manager, GCP Compliance Quality-R&D |
| Education:
Graduate degree in sciences, MD or PhD preferred
Professional Experience:
o Expert knowledge and understanding of all GCP related requirements, proficiency of regulatory and ICH guidelines
o Broad experience in clinical development in an industrial setting
o Demonstrated managerial skills in an international setting, with experience of at least 10 years in Clinical Development/Quality Assurance/Auditing
o Ability to work effectively in a team environment with great organization skills
o Excellent communication, negotiation and leadership skills
o Innovative and critical thinking, process and performance oriented. Constant drive to improve working practice |
| Novartis Oncology |
na |
CO |
11/20/2009
|
| Manager, US Project Management Supporting Broomfield Projects |
| Education/Experience:
BS in Science related field and 10-15 years of professional related experience or Graduate Degree and 5+ years related experience in the pharmaceutical industry (preferred experience across oral solid, injectable, ophthalmic and other dosage forms). |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Manager, US Project Management Supporting Global Projects |
| Education/Experience:
BS in Science related field and 10-15 years of professional related experience or Graduate Degree and 5+ years related experience in the pharmaceutical industry (preferred experience across oral solid, injectable, ophthalmic and other dosage forms). |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Manager, US Project Management Supporting Internal R&D Projects |
| Education/Experience:
BS in Science related field and 10-15 years of professional related experience or Graduate Degree and 5+ years related experience in the pharmaceutical industry (preferred experience across oral solid, injectable, ophthalmic and other dosage forms). |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Manager, US Project Management Supporting Specialty Projects |
| Education/Experience:
BS in Science related field and 10-15 years of professional related experience or Graduate Degree and 5+ years related experience in the pharmaceutical industry (preferred experience across oral solid, injectable, ophthalmic and other dosage forms). |
| Novartis Oncology |
na |
CA |
11/20/2009
|
| Manufacturing Manager (2nd shift)_SF Bay Area |
| Minimum Qualification Requirements:
? A minimum of a Bachelors degree in a scientific discipline is required. Equivalent experience may be accepted.
? A minimum of 8 years experience in GMP pharmaceutical manufacturing industry is required.
? A minimum of 5 years previous management experience preferably in a GMP manufacturing operation is required.
? Strong mechanical aptitude and hands on skills with tools and equipment are required.
? Familiarity with electronic test equipment and control systems is desired.
? Strong verbal and written communication skills are required.
? Must be goal-oriented, quality-conscientious, and customer-focused.
? Good laboratory compliance and safety practices are a must.
? Project management skills are preferred.
? GMP/ISO experience is required.
? Cleanroom experience may be required. |
| Novartis Oncology |
na |
NC |
11/20/2009
|
| Manufacturing Quality Manager |
| ? Bachelor?s Degree (minimum) in Technical Area (Chemical Engineering, Pharmacy, Biology, Chemistry)
? 7+ years experience in Quality Assurance, Quality Control or related technical field.
? Knowledge of contemporary quality systems and processes.
? Knowledge or PC tools including MS Word, Excel, Project or equivalent.
? Strong knowledge of GMP/Regulatory Validation requirements and industry standards.
? Knowledge of contract manufacturers/developers helpful.
? Ability to set priorities and manage multiple tasks.
? Effective interpersonal skills.
? Solid project management skills
? Strong management abilities.
? Excellent communication skills |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| MBA Brand Marketing Internship 2010 |
| This opportunity is limited to first year MBA students only.
? Internship with consumer packaged goods company or prior marketing experience a plus.
? Demonstrative strategic and creative problem solving skills
? Strong analytical skills and leadership skills particularly of cross-functional teams
? Excellent oral and written skills and proactive self-starter.
? Broad understanding of brand management principles.
? Knowledge of sales and marketing principles and awareness of market research methods.
? Computer efficiency required (Word, Excel, PowerPoint, Lotus notes preferred).
? Ability to analyze and summarize marketplace dynamics. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| MBA Summer Internship - Finance 2010 |
| 1st year MBA candidates that have experience in the areas of corporate finance (preferred). Candidates should possess strong analytical, interpersonal and project management skills and should also desire to become a participant in our Finance Leadership Development Program upon graduation to begin their career in finance within the Pharmaceutical industry. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| MBA Summer Internship - Marketing 2010 |
| 1st year MBA candidates that have experience in the areas of marketing and/or the pharmaceutical industry. Candidates should possess strong analytical, interpersonal and project management skills and should also desire to become a participant in our Commercial Development Rotational Program upon graduation to begin their career in marketing within the Pharmaceutical industry. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Medical Dir/Senior Medical Director US Medical NSO (Neuroscience) |
| A MD degree with 3-7 years? clinical trial experience and Board Certification/Eligibility in Neuroscience is required; direct pharmaceutical industry experience will be a plus.
? Experience in managing clinical trial conduct for neurological 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 neuroscience therapeutics and of bridging proactive relationships among product development, clinical development and marketing teams.
? Strategic business perspective required to bring launched and pre-launch compounds forward as commercially viable drugs.
? 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.
? Experience leading large projects/organizations.
? Excellent oral and written communication skills. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Medical Safety Expert II |
| Education:
MD required
Experience:
Minimum 5 years experience in health care or pharmaceutical industry with a minimum of 2 years in Drug Safety*, Minimum 1 year OTC ex-perience, Signal detection and risk management plan experience re-quired. Management experience preferred
*Experience requirement can be reduced with advanced education or equivalent relevant clinical experience |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| 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 |
CA |
11/20/2009
|
| 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 |
NE |
11/20/2009
|
| Mgr R&D QA & Compliance |
| Education: Minimum Bachelor of Science in Pharmacy, Chemistry, or other Scientific Disciplines
Experience:
? At least 8 years experience in the pharmaceutical, consumer health, or medical device industry in the areas of manufacturing, quality and regulatory systems, process development.
? QA and cGMP experience in Pharmaceutical, GMP and regulatory (GxPs) requirements including auditing and inspection against regulatory / quality standards.
? Demonstrated experience in managing multiple projects and deadlines.
? Good communication, planning, and organization skills.
? In depth understanding of pharmaceutical manufacturing, regulatory constraints, validation and product development.
? Excellent analytical, organizational, and problem solving skills.
? Good knowledge of computer systems, i.e. Microsoft, Word, Excel & PowerPoint.
? Demonstrated understanding best pharmaceutical industry practices, cGMPs, and Quality Assurance and Regulatory.
? Team oriented individual with personal commitment to human relations, integrity, giving and receiving constructive feedback, adaptability, diversity and communication. Must be adaptable to a diversified working environment. Experience in third party contract operations is preferred. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Molecular Pathologist |
| Education: DVM or MD, board-certified pathologist, MSc
Experience: Scientific experience and/or training as a molecular pathologist
Technical Ability: Technical and scientific experitise in ISH, IHC, immunofluorescence and knowledge in various aspects of molecular biology. Scientific experience in the development of novel protein and nucleic acid detection methods applied to tissue sections
Presentation: Good oral and written communication skills. Able to present data to peers and senior colleagues |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| 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 |
11/20/2009
|
| Molecular/Cellular Biology Research Scientist (BS/MS) |
| B.S or M.S scientist with at least 3 years of relevant research experience; the candidate has strong background in cellular and molecular biology. Previous experience in the study of innate immunity is highly desirable; experience in cellular immunology and in vivo biology is advantageous. 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 thinking. Excellent communication and organization skills are required. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| MS/ Ph.D Oncology Drug Discovery/ Target Validation Research Associate |
| The ideal candidate should possess a MS degree with 3-5 years of relevant biotech research experience. Candidates with a tumor biology Ph.D and relevant technical skills who are looking for a non-supervisory, technically driven position, are also 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 of a breadth of cellular and molecular biological methods (especially RNAi, RT-qPCR, cloning, cell culture, transient/ stable cell line generation, immuno-detection and phenotypic characterization). You should be a scientifically motivated self starter, capable of independently conceiving, conducting and critically analyzing your own innovative research with minimal supervision. Strong presentation skills, communication and the ability to work in a fast-paced team-oriented environment will also be vital. |
| Novartis Oncology |
na |
NY |
11/20/2009
|
| Multi-Skilled Craftworker II |
| ? Previous experience in Pharmaceutical, Packaging, or Manufacturing preferred.
? Minimum 5 years experience troubleshooting equipment malfunctions on electronic, pneumatic, and mechanical systems related to a manufacturing and packaging equipment.
? Experience supporting PLCs, HMIs/SCADAs, printing technologies (laser, inkjet, etc) vision/barcode systems, sensors, computer systems, industrial networks and motors (AC/DC drives, servo systems).
? The ideal candidate must be comfortable in an environment where he/she will be asked to troubleshoot equipment that is foreign to them.
? Comfortable working with and supporting computer based systems.
? Experience with continuous improvement environment (ie Lean, six sigma) a plus.
? Problem solving/critical thinking skills are required for detecting, analyzing, and resolving production problems
? Good interpersonal skills and communication skills are essential.
? Preferred: Two year degree in Automation or Electrical technology or equivalent engineering discipline.
? Certified Mechanic/Technician, Journeyman or an accredited training program certificate or equivalent. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Onco 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 |
11/20/2009
|
| Onco Dir Clinical Rsch Phys |
| Need 3-5 pharma/biotech industry experience in drug development - clinical trials. Must have Phase I Oncology proof-of-concept clinical trial designs expertise. Knowledge of PK/PD and basic statistics. Proven ability to analyze and interpret efficacy and safety data relating to assigned area Medical/scientific writing skills. Knowledge of GCP and world wide regulatory requirements relating to assigned area. Effective written and oral communication skills. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Onco Dir Clinical Rsch Phys |
| ? MD or PhD in Clinical Parmacology, Biochemistry or related field
? Substantial postgraduate bedside or clinical pharmacology experience in a relevant cancer treating discipline and institution required.
? Substantial experience with determining, administering, and evaluating the outcome of systemic combined modality cancer or adult hematologic malignancy treatment plans required.
? ? 3 years of involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV.
? Medical/scientific and operational expertise in cancer molecular medicine, biologics, and or response modifiers
? Demonstrated technical knowledge and innovation in early clinical development study designs that provide relevant evidence to decision-makers.
? Versatile knowledge and understand of pre-clinical science of oncology and all aspects of translational medicine such as toxicology, pharmacology, and regulatory requirements for early phase development in at least two relevant jurisdictions |
| Novartis Oncology |
na |
WA |
11/20/2009
|
| Oncol Area Sales Manager/Sr Area Sales Manager |
| Bachelor's degree required with a minimum of three years of pharmaceuticals sales management experience in the oncology, institutional, or specialty marketplace. Qualified candidates must have a demonstrated record of success in their ability to lead and inspire a sales team towards meeting and exceeding objectives, to communicate and implement tactical product strategies with a sophisticated audience, and to think strategically (i.e., "outside the box" and look at the "big picture") while providing creative and innovative solutions to market problems. Personal integrity and leadership abilities are essential. Excellent interpersonal, communication (both written and verbal), and presentation skills are required. Must be able to effectively multitask, problem-solve, and make decisions. Computer literacy (i.e., Word, Excel, and PowerPoint) is a must. As one of the largest pharmaceutical companies in the world and voted as one of the 100 Best Companies to work for by Working Mother Magazine, we are 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 |
NJ |
11/20/2009
|
| 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 |
MA |
11/20/2009
|
| Oncology Pharmacology PhD- PK/PD |
| A PhD degree in one of the life sciences, with expertise in in vivo physiology or pharmacology and at least three years postdoctoral and/or industry experience. Industry experience with oncology models is strongly preferred. The candidate should have a comprehensive, in-depth knowledge of Oncology research, particularly related to industrial drug discovery and development, with emphasis on drug combinations. He/she should have a strong background in molecular biology, biochemistry, developmental biology and a good knowledge of statistics. The candidate is also expected to be highly motivated, to have excellent leadership, communication and inter-personal skills. Experience in leading Oncology drug discovery programs and/or supervisory experience is a plus. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Operations Expert - Clinical Quality Assurance |
| Life-Science degree or equivalent. Project Management Certification.
8-10 years pharmaceutical industry experience preferred, with 5+ years in Clinical Development or Quality Assurance, with a detailed knowledge of clinical drug development process.
Audit experience strongly preferred.
Expert knowledge of international regulatory environment (GCP, at minimum US and EU regulations and ICH).
Demonstrated Project Management Training/Experience, or at least 2 years people management experience.
Demonstrated adult learning/training experience.
Ability to work globally and initiate and co-ordinate the work of associates at all levels required in managing global projects from initiation to completion.
Ability to communicate concepts and ideas verbally and in writing.
Good negotiation and interpersonal skills.
Expert planning and tracking skills.
Well organized.
Focused on results.
Capable of managing multiple projects / multi-tasking; excellent time management with respect to priorities and self management. |
| Novartis Oncology |
na |
CA |
11/20/2009
|
| 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 |
NJ |
11/20/2009
|
| Paralegal |
| Education : B.A./B.S. and/or Paralegal Certificate from ABA Certified Paralegal Studies Program
Experience: Minimum 5 years experience in all aspects of US patent prosecution including PCT. Experience with PAIR and electronic patent application filing. Experience learning different electronic data systems and synthesizing data systems together to create more efficient work processes. Strong interpersonal and teamwork skills. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Patent Attorney II |
| EDUCATION/EXPERIENCE:
Requires significant Hatch-Waxman experience, J.D./L.L.M., B.S. or M.S., preferably Ph.D. and 5-10 years related work experience. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Patent Attorney III |
| EDUCATION/EXPERIENCE:
Requires significant Hatch-Waxman experience, J.D./L.L.M., B.S. or M.S., preferably Ph.D. and 8+ years related work experience. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Patent Attorney, Chemistry |
| 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 |
MA |
11/20/2009
|
| Pathways Research Scientist (BS/MS) |
| ?BS or MS in Biochemistry, Molecular Biology, or Cell Biology, with 5+ years of laboratory research experience.
? Extensive experience with culturing various mammalian cell lines, utilizing both 2D and 3D culture systems, designing cell-based assays, generating stable cell lines, and executing small molecule screens with laboratory automation equipment.
? Experience with high content imaging and designing/executing high content imaging-based screens.
? Outstanding molecular biology techniques including complex DNA cloning, site-directed mutagenesis, and qPCR.
? Exceptional expertise in genetic screening with siRNA/shRNA/cDNA by conventional and viral transduction technologies.
? Proficient in various protein analysis techniques, including, but not limited to, ELISA assays, immunoprecipitations, and western blots.
?Excellent communication skills |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Ph.D Scientist: Oncology Biotherapeutics |
| Biotherapeutics lab head Qualifications:
? Ph.D. molecular biology or related field.
? Minimum 3 years of post-doctoral experience in cancer and/or antibody therapeutic research.
? Independent, self motivated and innovative personality
? Excellent written and oral communication skills
? Extensive experience in cell and biochemical assay development and analysis |
| Novartis Oncology |
na |
CA |
11/20/2009
|
| Pharmaceutical Sales Representative- Los Angeles, CA 5ZDL1A |
| A Bachelor's Degree * Outside sales experience with documented success in business-to-business sales preferred. * Professional accomplishments that reflect self-motivation, initiative, independence, and strong customer service orientation. In return, you'll be rewarded with: * An outstanding benefits package that includes a 401(K) and vision plan * An excellent salary and incentive awards program * A company automobile and paid expenses * Ongoing quality classroom and field training * Professional career development/growth opportunities and an educational assistance program. Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Pharmacogenetic Analyst (CP) |
| 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 |
MA |
11/20/2009
|
| Pharmacokinetics Research Scientist (BS/MS) |
| Candidates will need a M.Sc or B.Sc, or
equivalent in Pharmaceutical Sciences,
Pharmacology or related field.
Candidates possessing 3 or more years of
industrial experience in pharmacokinetics
and drug metabolism. Experience with pre-
clinical pharmacokinetic protocol design and
experience working with Watson or LIMS is
desirable. Proven ability to design and
manage both routine and mechanistic animal
PK studies and to prudently manage and
implement studies to drive drug discovery
efforts. Experience with non-compartmental
techniques and pharmacokinetic modeling
software (e.g., WinNonlin or equivalent) is
highly desired. A successful candidate will
need excellent interpersonal skills,
particularly oral and written communication
skills and the ability to multitask. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Pharmacovigilance Leader (PVL MD) |
| Experience/Professional:
3 years clinical experience postdoctoral
requirement:
At least 3 years in drug development in a major pharmaceutical company including 2 years in drug safety at an operational or medical position
Proven ability to analyze, interpret, discuss, and represent safety information both in writing and orally.
Experience in preparing or contributing to preparation of clinical safety assessments and regulatory reports/submissions involving safety information.
Experience with (safety or others) issue management
Experience in drug development, clinical trial methodology, regulatory requirements, scientific methodo logy, statistics and writing of publications
Education (minimum/desirable): Medical Degree required. Specialty Board certification desirable. Useful additional degrees: Post graduate degree in Pharmaceutical Medicine; Master of Public Health in Epidemiology (or equivalent) |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| PhD Medicinal/Synthetic Organic Chemist |
| * Ph.D. in synthetic organic or medicinal chemistry
* 2-6 years of relevant post doctoral or 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 |
11/20/2009
|
| PhD Research Investigator- Oncology Cellular Assay |
| The candidate should have a PhD. with 3+ years of experience in the pharmaceutical or biotech field,experience with developing new assays and transitioning them to HTS and a strong understanding of cellular biology and its relationship to cancer indications is a must. The ability to analyze large datasets for statistically relevant information, and experience with multiple automation platforms also required. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| 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 |
NJ |
11/20/2009
|
| Postdoctoral Fellow, DMPK |
| Ph.D. degree with 0-3 years of post-PhD research experience in pharmacokinetics, biopharmaceutics, biomedical engineering, chemical engineering, or other related discipline with specific experience in PK/PD and/or PK modeling is required. The candidate must be able to work independently and have a strong understanding of PK/PD. The candidate should should be able to provide technical assistance on individual projects, spanning across multiple therapeutic areas. Hands-on experience in PK and PK/PD modeling is a must. Good oral and written communication skills are required. Previous experience with some of the PKPD softwares such as: WinNonlin; ADAPT; NONMEM, GastroPlus. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| 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 |
NJ |
11/20/2009
|
| Principal MSE |
| MD or PhD with unique knowledge for successful clinical program development and execution, with > 6 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. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Principal Scientist (GMP Facility Manager/Engineer) |
| Education
Minimum: BS/MS or equivalent with greater than 8 years of experience.
Desirable: Advanced degree in a scientific or relevant discipline (Ph.D. or equivalent) with a minimum of 5 years of experience.
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 of 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. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Principle Med Scien Expert MD |
| ?Advance 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 nephrology/transplantation required. |
| Novartis Oncology |
na |
NC |
11/20/2009
|
| Process Validation Engineer III |
| EDUCATION/EXPERIENCE:
BS and 4 years of related experience in Pharmaceutical or related industry or MS and 2 years of related experience in Pharmaceutical or related industry or PhD and no significant experience |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Product Director/Assc Dir Regional Marketing Leader |
| Education: University degree in marketing or related
Fluent English and Spanish preferred
7-10 years operational marketing / product management experience (including Country-level product management, fast moving consumer goods branding or marketing support functions)
Pharmaceutical sales experience (minimum 6 months sales rep rotation)
International experience or worked with international marketing teams as a local product manager
Launch experience with new products or major line extensions
Experience in clinical development or Pharma project management
Experience in pharmaceutical brand/product communications
Exposure to multi-country product launches
Bilingual in English/Spanish is strongly preferred
Therapeutic areas of expertise - Oncology, Transplant, or AIDS is stongly preferred. |
| Novartis Oncology |
na |
CA |
11/20/2009
|
| Production Associate 2 |
| 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 |
