| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Year Round Information Systems Application Intern |
| Education/Experience Requirements: Qualified candidates will be currently enrolled in an undergraduate program, in at least your junior year of study; Candidates may also be in a graduate program, in an accredited program with a concentration in Information Technology along with business management or related field. Prior experience in a corporate business environment is preferred; experience in an Information Technology Department is a plus. Candidate should be good problem solvers and have understanding of basic algorithms. It is required that you have strong interpersonal, communication and time management skills as well as a proficiency in Microsoft Office (Word, Excel, and Power Point). Knowledge of using some of the following programming languages, software programs, technologies and/or skills is preferred: HTML, DHTML, JAVA, XML, CSS, and Database concepts |
| Agilent Technologies, Inc. US |
La Jolla |
CA |
9/4/2010
|
| Wireless Systems Application Engineer |
| Qualifications:
? BSEE or Masters degree in Engineering
? 5+ years hands-on experience with RF instrumentation including Spectrum Analyzers, Signal Sources, Power Meters
? 5+ years experience with Agilent Signal Studio, Agilent Vector Signal Analyzer, Matlab, or equivalent competitor design tools
? 3+ years hands-on R&D/development experience in Layer 1 (PHY) Wireless technologies such as GSM, GPRS, EGPRS, WCDMA (UMTS), HSPA, CDMA2000, 1xEVDO
? 3+ years hands-on experience with Cellular OBT?s such as Agilent 8960, R&S CMU200, Anritsu MT8820
Additional Skills:
? Familiarity with 3GPP, 3GPP2 (e.g. TS51.010, 34.121) test specifications
? Computer/IT admin skills; general system administration, setup, networking, and configuration mgt skills
? Software expertise; VB6, .NET, C#, Labview, scripting
? RF simulators; ADS, SystemVue
? Good customer communication skills; ability to lead customer facing technical discussions
? Office Tools; MS Word, Powerpoint, Excel, Visio, etc
? Excellent problem solving, diagnostic skills
? Strong trouble-shooting skills
? Strong team player |
| Agilent Technologies, Inc. US |
Columbia |
MD |
9/4/2010
|
| Wireless Network Engineer - Application Support |
| ?Bachelors or Masters Degree in Electrical/Electronic or Computer Engineering and 5+ years applicable experience in Mobile Communication Systems and Networks (including cell phone and other mobile communications infrastructure).
?Knowledge of wireless protocols, including: UMTS, GPRS, GSM and CDMA technologies
?Strong Linux/Unix system administration experience.
?Experience with Central Office networking
?Experience with Perl and Shell Scripting
?Experience with end user, installation and commissioning of new systems within customer environments is highly desired.
?Knowledge of Network Signaling is preferred
?Strong interpersonal/relationship skills, solid written and verbal communications.
?US citizenship is required, based on customer requirements
?Current high level US Government Security Clearance -or- ability to process for and obtain high level US Government Security Clearance.
Position is in Columbia, Maryland area. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| VP, Market Research |
| The ideal candidate is currently leading market research in a fast-moving consumer goods company or a consumer based health company. It is important that the individual be well versed in research methodology, understand the use of research tools and possess the ability to apply them to solve the company?s business problems. The individual must be a team player, have excellent communication skills, and must have proven leadership abilities.
People Leadership Skills: Successful candidate needs to be capable of leading and developing a strong team of capable Market Research associates. This includes driving results, empowering teams, building processes, managing performance and developing future leaders.
Strategic Marketing Skills: The successful candidate will have demonstrated the ability to identify unmet consumer needs and use consumer knowledge to evolve services and create effective marketing strategies. This person will have a demonstrable record of standing in the end-users shoes, and motivating behavioral change one step at a time.
?Excellent Analytical Acumen: The successful candidate will have demonstrated the ability to assess disparate data streams and distill them into meaningful and, ultimately, actionable strategic recommendations. This encompasses consumer, constituent and competitive environments. A track record of identifying profitable consumer segments and separating those from unprofitable ones is a necessity. Identifying competitor?s intent before they take action is required.
?New Product Concept Development: This person will have a record developing new product concepts from fact-based analysis with a strong end-user orientation. He or she will have worked closely with technical product development teams to actualize the product.
?End-Consumer Orientation: The information resources are highly targeted due to the well-defined target audience. Therefore, the successful candidate will have extensive success with highly customized research protocols, and not be as reliant on broad-based psycho/demo-graphic studies. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| VP, Global Purchasing |
| 10+ years of Procurement experience, 3+ years in the healthcare industry or equivalent. Significant leadership experience, extensive experience in terms of leading and developing teams within a matrix organization and across geographies and cultures. Extensive experience change and category management.
Bachelor?s degree required at a minimum, master?s degree preferred; in fields such as business administration, finance, law or a scientific or technical field. Strong preference for CIPS or similar professional qualification. |
| Ogilvy CommonHealth Worldwide |
Parsippany |
NJ |
9/3/2010
|
| VP Management Supervsior |
| Must have at least:
•8+ years in business
•8+ years marketing advertising agency experience on professional marketing accounts
•6+ years in healthcare/pharmaceutical marketing
•6+ years as a leader of account management personnel
•Minimum four (4) year degree required; Master’s Degree/MBA a plus
•Strong knowledge of the pharmaceutical and healthcare industry
•Oncology experience preferred, prostate experience a plus
•Outstanding leadership skills
•Outstanding team building skills
•Experience managing a brand and coordinating multiple disciplines required (i.e. professional, consumer, digital, med ed)
•Innovative thinker who also has the ability to foster innovative thinking in others
•Proven relationship building with client Brand Managers, Team Leaders, and Directors of Marketing (or equivalent)
•Can point to meaningful successes that they have "owned"
•Track record of innovative business solutions and successes
•Excellent communication, presentation and time management skills
•Writes extremely well -- writes presentation decks on their own
•Sound financial skills -- has prepared budgets, staffing plans, and statement/scope of work plans
•Centrally engaged in the agency process (not a peripheral player or bench-warmer)
•Detail-oriented, drives for results
•High strategic fluency
•High digital fluency
•Production and process fluency – must be able to help with process when necessary
•Experience working within a pharmaceutical company is a plus
•Launch experience a must
•Microsoft Excel and PowerPoint proficiency is a plus
We are an equal opportunity employer. |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Vice President, Market Development, HAI |
| See above |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Vice President, Global Clinical Science |
| Minimally a BS Degree. Must have at least 15 years of pharmaceutical industry experience specifically in human drug development, and at least 3-5 years managing managers of multiple groups within the area of Clinical Operations/Clinical Science. Previous experience in leading a Global Clinical Operations function is preferable. Must have a successful track record in the hiring and retention of excellent clinical operations resources globally, who work optimally in a cross functional team and matrix environment. Must have a successful track record in effectively collaborating with other functions in development, discovery research, Medical Affairs and Commercial in the development and support of medicines. |
| Teva Pharmaceuticals USA |
Irvine |
CA |
9/4/2010
|
| Validation Engineer I |
|
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
9/3/2010
|
| Validation Engineer (Computer) |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
9/3/2010
|
| Validation Engineer (Computer) |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
9/3/2010
|
| Validation Engineer |
| See above |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| US IS Domain Architect - Web |
| * Bachelor's degree in relevant field.
* Minimum 10 years cumulative experience in architecture and supporting methodologies, with at least 5 years in the domain(s) of focus
* A broad understanding of architecture covering all aspects from business/process, information, application to infrastructure architecture.
* Working knowledge of necessary operating model components to support architecture implementation and adoption.
* Strong analysis, conceptual thinking and modeling capabilities.
* Strong relationship management, strategic influencing, and communication skills.
* Delivery focused and creative in finding ways of delivering.
* Ability and desire to work globally and see this as a great opportunity.
* Ability to work independently across the global organization while overseeing the work of others.
Preferred Background
* Advanced degree in relevant field
* Large scale project management experience
* Cross-functional team experience
* Evidence of strong leadership
* Accomplished facilitation and negotiating skills |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
9/3/2010
|
| Tubes Technical Associate |
| See above |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Traning Solution Partner (Development) |
| Masters Degree (or adequate) preferred, candidates with previous working experience in pharmaceutical industry preferred; 5+ years HR/Training experience required; scientific education is an additional advantage.
Fluent in English, other languages are an additional advantage. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Training Manager, Reclast |
| ? Bachelor?s degree
? Strong written, oral communication skills
? Extensive therapeutic experience,
? 3-4 years of pharmaceutical sales experience
? Strong clinical & Therapeutic knowledge
? Brand strategy, tactics understanding
? Partnering Skills (brand, medical, PRC, vendors etc)
? Presentation and platform skills. Ability to communicate in small and large settings
? Knowledge of field /sales force (key client knowledge)
? Administrative management skills - planning, organization, operational decision making and analysis.
? Creativity and innovation.
? Thorough knowledge of pharma industry, Novartis products and competition.
? Ability to manage multiple projects
? Fluent English (oral and written) |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Trade Analyst ? USMM Trade Operations |
| BS/BA degree required.
Minimum of 2-4 years of analytical experience.
Must have at least 2 years in the pharmaceutical industry specifically in trade operations, sales and distribution or customer support.
Strong working knowledge of SAP, Sales and Distribution module and Business Warehouse.
Preferred experience of reporting within SAP
Good problem solving, decision, verbal and written skills
Effective interpersonal and organizational skills
Must have the ability to plan and organize work with multiple priorities.
Computer literacy is required, Microsoft Office, Excel, Word, PowerPoint, and Access
Strong working knowledge of DEA & FDA regulations |
| BD (Becton, Dickinson and Company) |
Broken Bow |
NE |
9/3/2010
|
| TOOLING ENGINEER |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus West |
NE |
9/3/2010
|
| Tig Weld thru - Cut - D Shift |
| See above |
| Novartis Oncology |
na |
DC |
9/4/2010
|
| Territory Sales Representative- Washington, DC |
| Minimum Experience Required:
2-4 years successful outside sales experience in a business-to-business selling model.
Preferred Level:
A combination of business-to-business selling experience, at least One (1) year contact lens sales/ophthalmic related sales/contact fitting experience, and/or medical sales experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel also required. Must successfully complete our "New Hire Sales Training Program".
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
NV |
9/4/2010
|
| Territory Sales Representative- Las Vegas North/Reno |
| Minimum Education Required:
Bachelor's degree or equivalent
Minimum Experience Required:
2-4 years successful outside sales experience in a business-to-business selling model.
Preferred Level:
A combination of business-to-business selling experience, at least One (1) year contact lens sales/ophthalmic related sales/contact fitting experience, and/or medical sales experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel also required. Must successfully complete our "New Hire Sales Training Program".
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
KY |
9/4/2010
|
| Territory Sales Representative- Bowling Green, KY |
| Minimum Education Required:
Bachelor's degree or equivalent
Minimum Experience Required:
2-4 years successful outside sales experience
Preferred Level:
One (1) year contact lens sales/ophthalmic related sales/contact fitting experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel also required.
Must successfully complete our "New Hire Sales Training Program".
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
VA |
9/4/2010
|
| Territory Sales Representative Virginia Beach, VA |
| Minimum Education Required:
Bachelor's degree or equivalent
Minimum Experience Required:
2-4 years successful outside sales experience in a business-to-business selling model.
Preferred Level:
A combination of business-to-business selling experience, at least One (1) year contact lens sales/ophthalmic related sales/contact fitting experience, and/or medical sales experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel also required. Must successfully complete our "New Hire Sales Training Program".
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Territory Sales Representative Johnstown, PA |
| Minimum Education Required:
Bachelor's degree or equivalent
Minimum Experience Required:
2-4 years successful outside sales experience in a business-to-business selling model.
Preferred Level:
A combination of business-to-business selling experience, at least One (1) year contact lens sales/ophthalmic related sales/contact fitting experience, and/or medical sales experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel also required. Must successfully complete our "New Hire Sales Training Program".
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
MO |
9/4/2010
|
| Territory Sales Representative - St. Louis, MO |
| Minimum Education Required:
Bachelor's degree or equivalent
Minimum Experience Required:
2-4 years successful outside sales experience in a business-to-business selling model.
Preferred Level:
A combination of business-to-business selling experience, at least One (1) year contact lens sales/ophthalmic related sales/contact fitting experience, and/or medical sales experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel also required. Must successfully complete our "New Hire Sales Training Program".
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
NC |
9/4/2010
|
| Temporary HR/Compensation Analyst |
| Education : Bachelors degree
Experience: 1-3 yrs of Compensation/Benefits and/or Generalist experience, preferably Peoplesoft and SAP experience. Ability to manage sensitive employee information in a confidential manner. |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Staffing Assistant |
| * Bachelor?s degree or equivalent required.
* 0-4 years experience working on a fast-paced, high-volume HR team, or several years in a fast-paced administrative environment.
* Exceptional organizational and communication skills, and computer proficiency in MS Office and/or Lotus Notes required.
* Applicants must be able to manage multiple tasks and address issues with a sense of urgency, handle sensitive situations and confidential materials with tact, and challenge conventional practices by introducing new ideas and process improvements.
* Must be able to interact and communicate effectively with all levels in and outside the organization and demonstrate a strong customer service.
* Strong team players and those with high attention to detail are urged to apply.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Sr. Statistical Programmer |
| Experienced with all SAS language, procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH.
Experienced with the CDISC SDTM and AdaM models and transforming raw data into these standards.
Experienced working with all types of safety data and coding dictionaries (MedDRA and WHODRL) commonly used by the pharmaceutical industry.
Experienced working in a team environment providing technical leadership and solving clinical trial reporting problems of moderate to high complexity within budget and customary time line constraints while assuring high quality standards.
Skilled at performing quality control checks of SAS code and output produced by other Statistical Programmers.
Knowledgeable regarding software validation and system development life cycle concepts.
B.S. in Biostatistics, Statistics, Computer Science, or a related field and a minimum of 5 years of SAS and relevant pharmaceutical industry experience.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Sr. Scientific Associate |
| Preferred Education and Experience:
- A Bachelor's degree in the life sciences or physical sciences with a preference for a concentration in Chemistry, Analytical Chemistry or Pharmaceutical Chemistry with 3-5 years related experience.
- Working understanding of DISSOLUTION, HPLC, LC-MS, GC, GC-MS, FT-IR, UV-VIS, KF, and other instruments used in the analysis of pharmaceutical products
- An interest in and passion for establishing a career in analytical development and the biopharmaceutical industries
- The ability to work successfully in both a team environment as well as independently
- Excellent written and verbal communication skills
- Established organizational skills
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Sr. Scientific Associate |
| * Bachlor's degree in Chemistry, pharmaceutical sciences, or equivalent concentration.
* 0-3 years experience in an analytical capacity;
* Have received general training/coursework on analytical instruments;
* Able to conduct dissolution analysis on solid oral dosage forms (training will be provided);
* Have an understanding of the theory of analytical development, general HPLC use and care;
* Awareness of USP dissolution methods
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Sr. QA Specialist |
| PREFERRED EDUCATION AND EXPERIENCE:
* M.S. (or equivalent degree) and 0 ? 3 years of relevant work experience, or
* B.S. in a scientific or allied health field (or equivalent degree) and 5 ? 8 years of relevant work experience
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Sr. Engineer |
| Job Requirements:
? Minimum 5 years IT experience in an Infrastructure support role specializing in storage management
? Strong technical, analytical, and troubleshooting skills with experience in troubleshooting multi-tier environments
? Excellent communication skills - both written and verbal. Must be able to communicate with all team members, both technical and non-technical
? Self-motivated with strong organizational skills, the ability to juggle multiple high-priority tasks and maintain attention to detail.
? Experience working with teams in different time zones and coordinating duties to coincide with global operational schedules.
? Strong experience working with Enterprise SAN/NAS architecture, protocols, and best practices (EqualLogic, HP, NetApp)
? Solid understanding of storage interface technologies such as iSCSI and Fibre Channel.
? Experience operating in a Brocade SAN fabric environment (certification a plus)
? Proven storage provisioning skills, including disk assignment, and LUN masking
? Working knowledge of Enterprise LAN/WAN network architecture, protocols, and best practices as related to iSCSI (Cisco certification or equivalent a plus)
? Working knowledge of UNIX, Linux and Microsoft Windows Server (certifications a plus)
? Experience with data migration tools: robocopy, richcopy, rsync, dump, tar, etc.
? Experience with Enterprise monitoring systems (Nagios a plus)
? Pharmaceutical & FDA regulated experience a plus, experience supporting a Research environment a plus
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Scientist I |
| A Ph.D. or Master's or Bachelor's degree in the life or physical sciences with a preference for a concentration in Chemistry, Analytical Chemistry or Pharmaceutical Chemistry
- 0 - 3 years (PhD), 3 - 5 years (MS) or 6+ years (BS) current relative industry experience working in drug substance and drug product support
- Broad awareness of the drug development process, including clinical design, chemical development, and formulation development, especially how those processes impact analytical method development, validation, and method transfer are essential
- Good understanding of GMP and hands-on GMP experience as well as how to develop methods that are GMP friendly are preferred.
- Have received general training/coursework on analytical instruments;
- Working knowledge of analytical instrumentation such as HPLC, GC, UV-VIS, LC-MS, KF, and dissolution apparatus required.; experience with USP IV flow through apparatus a plus.
- Solid experience with HPLC-UV method development preferred.
- Strong capabilities with Excel or other spreadsheet based applications, statistically training a plus.
- The ability to work successfully in both a team/matrix environment as well as independently;
- Familiarity with various sold dosage forms: including tablets, capsules, and solid dispersions is desirable;
- The ability to work in a fast pace environment, manage priorities, and maintain timelines for multiple projects
- Excellent written and verbal communication skills, including familiarity with Scifinder and other journal databases
- Established organizational skills
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Scientist I |
| Minimum requirements:
- A Ph.D. or Master's or Bachelor's degree in the life or physical sciences with a preference for a concentration in Chemistry, Analytical Chemistry or Pharmaceutical Chemistry
- 0 - 3 years (PhD), 3 - 5 years (MS) or 6+ years (BS) current relative industry experience working in drug substance and drug product support
- Broad awareness of the drug development process, including clinical design, chemical development, and formulation development, especially how those processes impact analytical method development, validation, and method transfer are essential
- Good understanding of ICH and FDA method validation guidelines are essential. The ability of identifying areas overlooked in the guidelines is preferred.
- Good understanding of GMP and hands-on GMP experience as well as how to develop methods that are GMP friendly are preferred.
- Working knowledge of analytical instrumentation such as HPLC, GC, UV-VIS, LC-MS, KF, and dissolution apparatus required.; experience with USP IV flow through apparatus a plus.
-Solid experience with HPLC-UV method development preferred.
- Strong capabilities with Excel or other spreadsheet based applications, statistically training a plus.
- The ability to work successfully in both a team/matrix environment as well as independently;
- Familiarity with various sold dosage forms: including tablets, capsules, and solid dispersions is desirable;
- The ability to work in a fast pace environment, manage priorities, and maintain timelines for multiple projects
- Excellent written and verbal communication skills, including familiarity with Scifinder and other journal databases
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Scientific Associate II |
| Minimum Education Requirements:
Bachelor?s degree in science or engineering field. Internship or undergraduate research project involving analytical laboratory work strongly preferred.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Research Associate I |
| Experience working in a laboratory with skills in cell culture and standard molecular biology techniques (e.g., cloning and PCR) is required. Additional knowledge or experience in cell-based assays is desired. Meticulous attention to the details and regular maintenance of laboratory notebooks is required. The successful candidate must be a demonstrated team player and be able to work closely and responsively with their supervisor. Applicant must be able to follow appropriate biosafety procedures for working in an infectious disease laboratory.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. QA Specialist |
| * Bachelor's degree preferred
* 2 years of experience in Quality
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Manager, Health Value & Outcomes Research |
| Minimum Requirements:
? A bachelor?s degree in the life sciences, business administration or a related field with a preference for an advanced degree (MD, PharmD, MPH, MS, MHA or MBA). Educational focus in the areas of health economics or outcomes research would be beneficial
? 3 - 5 years of current experience with health economics and outcomes research for the biotechnology or pharmaceutical industries
? Working experience with economic modeling and payer market access tool creation
? Familiarity with payer dossiers, epidemiology, economic analyses, reimbursement and pricing environments
? A track record of success functioning in dynamic, matrix environments with the ability to multitask and adapt to rapid changes
? Exceptional written and verbal communication skills along with the ability to interact constructively across all levels of an organization and with thought leaders and other external collaborators
? The ability to effectively present technical data and complex concepts to diverse audiences
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Lead Engineer |
| Job Requirements:
? A minimum of 8 years experience with CommVault (Enterprise Backup System) backing up servers, databases, SAN and NAS Storage.
? Strong knowledge of Enterprise Tape Libraries (Quantum a plus) and LTO-X technologies.
? Linux administrative experience (RedHat 5.x a plus)
? Windows administrative experience (Windows 2008 a plus)
? Basic networking skills
? Ability to function effectively in a fast-paced environment, handles multiple tasks simultaneously, and meets deadlines.
? 5+ years experience in a 700+ server environment across multiple sites
? Excellent communication skills both written and verbal
? Self-motivated with outstanding troubleshooting experience
? Research, Pharmaceutical & FDA regulated experience a plus
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The company's strategy is to commercialize its products bother independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, inflammation, autoimmune diseases, cancer, pain and bacterial infection.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Clinical Staffing Consultant |
| Minimum Requirements
· 5+ years pharmaceutical clinical or medical recruiting experience a must, minimum of a Bachelors degree or equivalent
· Experience working in a fast-paced, highly matrix organization
· Proven track record of finding unique ways to source and attract qualified candidates
· Superior selection skills and a high level of proficiency in assessing individuals
· Proven ability cultivating successful relationships internally and externally
· Results driven, ability to demonstrate/quantify success relative to established targets and metrics
· Strong listening, facilitation and communications skills
· Strong organizational, multi-tasking and computer and web skills, along with the ability to handle sensitive and confidential situations/information
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp QA Specialist |
| * B.S (or equivalent degree) and 3-5 years of relevant work experience
* Experience with analytical testing and data review in a GMP environment.
* Experience with the following analytical techniques desirable; HPLC, GC, Dissolution, KF moisture, TGA, FTIR, NMR, UV, wet chemistry. (With emphasis on HPLC and GC experience)
* Reference standard testing.
* Non-conformance or laboratory investigation experience.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Technical Writer |
| See above |
| Novartis Oncology |
na |
CO |
9/4/2010
|
| Technical Services Scientist |
| ? BS degree required (Engineering or Pharmacy is preferred)
? 6 years related experience with BS Degree
?4 years related experience with MS Degree
? 2 years related experience with PhD Degree
Competencies:
?Technical Competence
? Solid Knowledge of cGMP and FDA regulations and guidelines
? Good Written and Verbal Communication Skills
?Speed/Action/Simplicity/Initiative |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Technical Service Contact Center Manager |
| See above |
| Miltenyi Biotec Inc. |
San Diego |
CA |
9/3/2010
|
| Technical Sales Consultant - San Diego |
| 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=502699 |
| Miltenyi Biotec Inc. |
Orlando |
FL |
9/4/2010
|
| Technical Sales Consultant - Orlando, FL |
| 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=521160 |
| Miltenyi Biotec Inc. |
Oakland |
CA |
9/3/2010
|
| Technical Sales Consultant - Bay Area, CA |
| 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=517835 |
| Miltenyi Biotec Inc. |
|
|
9/4/2010
|
| 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
|
| BD (Becton, Dickinson and Company) |
St. Louis |
MO |
9/3/2010
|
| Technical Applications Specialist-Research Flow Cytometry |
| See above |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Team Leader II, ARD |
| PhD, Chemistry or closely related scientific field, with 3-5 years of related pharmaceutical experience. MS, Chemistry or closely related scientific field, with 5-7 years related pharmaceutical experience. BS, Chemistry or closely related scientific field, with 7-10 years related pharmaceutical experience. Minimum of 2-4+ years previous and demonstrated supervisory experience. |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Tax Analyst |
| Minimum Requirements
* Associate's Degree in business, accounting or finance or equivalent work experience of 2- 5 years experience in accounting, tax or finance in a large corporation or accounting firm..
* Excellent knowledge of Excel computer software.
* Excellent interpersonal skills.
Preferred Background:
* Undergraduate Accounting Degree in Accounting or Finance.
* Prior work experience or co-op or internship experience in a Tax Dept.
* Experience with tax research software and business writing. |
| AstraZeneca Pharmaceuticals |
Waltham |
MA |
9/4/2010
|
| TA Medical Scientist-Oncology |
| Minimum Requirements --Education and Experience
* Relevant Clinical or Biomedical Ph.D or relevant Pharmacy, Msc/Mres degree with significant R&D experience
* 3-5 years of clinical drug development or medical affairs experience within a pharmaceutical company environment
* A degree of specialist knowledge of the medical and scientific activities related to a particular therapeutic area/indication and/or to an assigned project or product
* A good understanding of more than one development function
Skills and Capabilities
Leadership Capabilities- Level 2
* Passion for Customers
* Thinks Strategically
* Acts Decisively
* Drives Performance
* Works Collaboratively
* Develops People and Organizations
Additional Skills and Capabilities
* General Scientific & Medical understanding
* Ability to acquire and assimilate knowledge in different disciplines, disease and therapeutic areas
* Ability to credibly influence whilst maintaining independent and objective views
* Communication, interpersonal and organizational skills
* Attention to detail
* Analytical thinking
* Cultural awareness
* Commercial acumen
Internal and External customers/contacts
* Clinical Partnerships
* Investigators and KOLs
* Clinical Development functions eg., patient safety, regulatory,
* Clinical Biomarker Group
* Global Marketing, ISMO and marketing companies
* Discovery/Translational Science
Reporting Relationship
* Reports to GD or TACD |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Systems Validation Specialist II |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Systems Validation Specialist II |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Systems Validation Specialist II |
| See above |
| Teva Pharmaceuticals USA |
Irvine |
CA |
9/4/2010
|
| System Administrator/Business Analyst II IT |
|
| BD (Becton, Dickinson and Company) |
Holdrege |
NE |
9/3/2010
|
| Syringe Specialist-All Shifts |
| See above |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Surveillance Application Engineer |
| Bachelors or Master Degree or University Degree or equivalent plus a minimum of 3 years relevant experience, with typically 5 to 8 years practical experience. |
| Agilent Technologies, Inc. US |
Wilmington |
DE |
9/4/2010
|
| Support Agreement Sales Specialist |
| To join our dynamic and high-achieving team, you need:
? BA/BS/MS degree in Science or Business-related field; or equivalent
? Experience in customer facing or sales role (entry 0-4 years experience, career 3 - 8 years)
? Competitive selling experience preferred
? Ability to work in a fast paced, dynamic team environment.
? Excellent verbal and written communication skills a must.
? Strong desire to interact directly with customers (via phone, email)
? Must have proficient computer skills; experience in use of database S/W applications such as Siebel, and Microsoft Office etc.
? Available for 10% travel. |
| Agilent Technologies, Inc. US |
Boulder |
CO |
9/4/2010
|
| Supply Chain Manager |
| Key qualifications and/or experience for the position.
Education:
Advanced degree in Chemistry or MBA (emphasis in supply chain management preferred)
Experience:
Minimum of 10 years strategic sourcing experience in pharmaceutical or specialty chemical manufacturing
Demonstrated ability to develop strategic sourcing plans
Contracts preparation and management experience
Inventory management experience
International experience in logistics, transportation and distribution of raw materials
Functional expertise with Supply Chain Management systems
Professional Skills:
Strong interpersonal skills, strong organizational skills, and ability to analyze complex data
Project management or client/supplier relationship management experience
Ability to work effectively in an interdisciplinary and cross functional team environment
Analytical chemistry knowledge with the ability to set, justify and negotiate specification
In depth understanding of the connection between raw material quality, specifications and final product quality
Leadership Skills
The successful candidate will have a demonstrated ability to affect change in high growth business environment and motivate direct and indirect assets to achieve challenging goals.
Computer Skills
Proficiency in the use of MS office applications and relational data base management
Understanding of SAP, Oracle, MRP or other financial/inventory management systems |
| Novartis Oncology |
na |
CO |
9/4/2010
|
| Supervisor, Production - 3rd Shift |
| ? BA/BS and 4 plus years of professional related experience or Associate Degree or technical degree equivalent and 6 plus years of related experience
? Supervisory experience in a production environment preferred
? Technical training of pharmaceutical processes and equipment
? Proficiency in operation and trouble-shooting of the packaging/production equipment preferred
? Knowledge of general process improvement theory, customer service practices, coaching and counseling approaches, and conflict management techniques.
? Ability to write equipment and operation procedures and review, assess and write technical reports
? Ability to handle compliance issues with a sense of urgency and accuracy
? Strong Customer/Quality focus
? Strong written and verbal communication skills
? Results oriented
? Demonstrated ability to apply Lean/6 Sigma concepts and to identify continuous improvements to increase equipment efficiency |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Study Support Associate II |
| ? 2-year degree in Veterinary Sciences or related animal management field, 4-year Science degree, or an equivalent amount of prior experience required.
? Thorough understanding and comprehension of operational facts, techniques, nomenclature, equipment, theories, etc. as they relate specifically to job performance and function in the laboratory animal research environment.
? Certified Veterinary Technician (CVT), AALAS LAT/LATg, and/or similar certification required.
Strong communication skills
Minimum 3 - 5 years experience in a technical skills tract laboratory animal program required. Weekend work will be required. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Study Support Associate I |
| ? 2-year degree in Veterinary Sciences or related animal management field, 4-year Science degree, or an equivalent amount of prior experience required.
? Thorough understanding and comprehension of operational facts, techniques, nomenclature, equipment, theories, etc. as they relate specifically to job performance and function in the laboratory animal research environment.
? Certified Veterinary Technician (CVT), AALAS LAT/LATg, and/or similar certification required.
Strong communication skills
Minimum 3 - 5 years experience in a technical skills tract laboratory animal program required. Weekend work will be required. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Study Support Associate I |
| BS/MS in biomedical science, pharmacology, or related discipline. Hands-on experience with animal models is essential, and the selected candidate should also have experience in virology and/or bacteriology is preferable. An understanding of pharmacokinetics is desirable. The candidate should also have experience in experimental design, animal surgery, microbiology techniques, data interpretation, and statistical analysis. A strong work ethic, excellent oral and written communication skills, and the ability to function in an interdisciplinary team are essential. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Strategic Alliances Negotiator |
| Minimum requirements An Bachelor?s or Master?s Degree is a scientific area is desired, as is either an MBA or a JD, the Strategic Alliances Negotiator will possess an excellent in-depth
knowledge of the pharma/biotech arena, and will
have at least five years experience in a licensing or business development role. He or she will have a demonstrated capability for completing high quality transactions.
Experienced in partnering with biotechnology companies and/or academic/research institutions, he
or she will possess superior analytical, strategic and
communication skills. Well organized, detail oriented,
with a strong sense of urgency, the Negotiator will be a
team player comfortable working in a global matrix
system. A creative thinker, he or she will establish
innovative business solutions and concepts with a
strong strategic vision, consensus building talent,
negotiation skills, and a strong entrepreneurial spirit.
Considered reliable, pro-active, hands-on, able to
manage projects and function with autonomy, he or
she will understand how to influence people and
situations in an R&D setting. |
| Chantest |
Cleveland |
OH |
9/3/2010
|
| Staff Scientist - Electrophysiology |
| Minimum qualifications are a BS/BA in biology, chemistry or related science with at least one year of laboratory experience. Prior experience in an electrophysiology laboratory is a plus, but is not required.
ChanTest provides a competitive benefits package. Salary is commensurate with experience. Please send your resume with salary requirement to: humanresources@chantest.com or fax to 216-332-1706. Equal Employment Opportunity. |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Staff Engineer- Pen Injection Platform |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Staff Engineer or Scientist - Optical Engineering |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Staff Engineer or Scientist - Chemical Engineering and Biocompatibility |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Staff Engineer Core Team Leader |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Staff Engineer - Core Team Leader |
| See above |
| Daiichi Sankyo, Inc. |
Edison |
NJ |
9/3/2010
|
| Staff Biostatistician |
Education/Experience Qualified candidates must have a MS or PhD in Statistics, Biostatistics, or Mathematics. PhD + 8 yrs or MS + 10 years of pharmaceutical industry experience; full knowledge of advanced statistical analytical methods, clinical trial research, regulatory requirements, coding techniques, and statistical software. Excellent oral and written communication skills; project planning skills; demonstrated experience in analyzing clinical trial data; priority setting skills; multi-tasking skills; problem solving skills; eye for detail; exercise good judgment; and works well within team framework. Comprehensive project management skills.Demonstrated competency in SAS. Regular attendance at IDT Meetings is necessary; experience in managing CROs and external vendors. Must be willing to travel 10% of the time. |
| Daiichi Sankyo, Inc. |
Edison |
NJ |
9/3/2010
|
| Staff Biostatistician |
| Education/Experience Qualified candidates must have Statistics, Biostatistics, or Mathematics: MS or PhD. PhD + 8 yrs or MS + 10 years of pharmaceutical industry experience; full knowledge of advanced statistical analytical methods, clinical trial research, regulatory requirements, coding techniques, and statistical software. Excellent oral and written communication skills; project planning skills; demonstrated experience in analyzing clinical trial data; priority setting skills; multi-tasking skills; problem solving skills; eye for detail; exercise good judgment; and works well within team framework. Comprehensive project management skills. Demonstrated competency in SAS. Regular attendance at IDT Meetings is necessary; experience in managing CROs and external vendors. |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Staff Accountant |
| Education:
BS with a major in Accounting, CPA, MBA preferred
Experience:
One to three years experience in an accounting environment, preferably within a pharmaceutical company.
Preferred Skills/Qualifications:
Microsoft suite of software (Excel, Word, etc..).
Experience with Oracle Financial Software a plus
Skills/Competencies:
Excellent communication and organizational skills.
Ability to work independently with strong attention to accuracy and detail
Other Skills:
Ability to communicate effectively with higher levels of management.
Vertex Pharmaceuticals |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Sr.Engineer/Ass. Staff Engineer |
| B.S. degree in physics, chemistry, or electrical engineering or equivalent, plus a minimum of 7 years of related experience, or an equivalent combination of M.S or Ph.D. degree and experience. Advanced degree and minimum of 6 years of relevant experience required for Staff Engineer.
*NMR experience, NMR systems experience and good operating knowledge of VNMRJ are strongly preferred.
*Good RF, analog, and digital electronic experience and operation of related test equipment required. And/or experience with High Powered RF preferred
*Mechanical engineering and machine shop experience a plus.
*Unix/Linux operating knowledge, basic CAD experience, and knowledge of MS Office required.
Strong analytical and troubleshooting skills are required.
*Good verbal and written communications skills. |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Sr. Systems Analyst-Enterprise ETL |
| ? Languages: SQL, PL/SQL, Java, scripting languages
? Databases: Oracle 11g (preferred), 10g
? OS: Linux, Windows
Preferred technical skills (a plus):
? Enterprise ETL Platform (Talend, Informatica, Datastage)
? Data Warehouse design and modeling (Oracle preferred)
? Master Data Management experience (Siperian preferred)
? Experience with all phases of software development, including requrements, design, development and testing
Technical and Communication Skills:
? Ability to work interactively with users, management and support team.
? Ability to work within established coding and documentation standards
? Team contributor with good communication skills and strong analytical, problem solving skills.
Preferred Education and Experience Levels:
? B.S and 5 years relevant work experience
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Sr. Systems Analyst-BI Reporting |
| Minimum Requirements
? Enterprise BI Reporting platform (MicroStrategy, Noetix, Cognos)
? Languages: SQL, PL/SQL, Java, scripting languages
? Databases: Oracle 11g (preferred), 10g
? OS: Linux, Windows
Preferred technical skills (a plus):
? Data Warehouse design and modeling (Oracle preferred)
? Experience with all phases of software development, including requrements, design, development and testing
? Experience with Extract-Transform-Load processes and batch data movement at the enterprise level
Technical and Communication Skills:
? Ability to work interactively with users, management and support team.
? Ability to work within established coding and documentation standards
? Team contributor with good communication skills and strong analytical, problem solving skills.
Preferred Education and Experience Levels:
? B.S and 5 years relevant work experience
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Teva Pharmaceuticals USA |
Irvine |
CA |
9/4/2010
|
| Sr. Supervisor/Supervisor Microbiology (2nd Shift) |
|
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Sr. Scientist/Scientist, Cell Culture Process Development - Agensys, Santa Monica, CA |
| ? Ph.D. in a scientific discipline (Chemical Engineering, Biochemical Engineering or biology) with 5+ years of relevant experience in the pharmaceutical /biotechnology industries.? Knowledge of the design, optimization and scale-up of cell culture processes is a necessity. Direct experience with mammalian cell culture process development and process transfer for clinical or commercial manufacturing of biopharmaceutical product(s) highly preferred.? Knowledge in the use of DOE to conduct experiments? Hands-on experience with unit operations such as lab and pilot-scale bioreactor operation,centrifugation, clarification, and filtration.? Process validation and cGMP experience is desirable.? Supervisory experience preferred.? Must be highly motivated, have excellent organizational and communication skills, and must be able to work independently and as part of a multi-disciplinary team |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr. Scientist, Research |
| 9-13 Years with Bachelors of Science, 7-11 Years with Master of Science, 4-8 Years with PhD. |
| Novartis Oncology |
na |
CO |
9/4/2010
|
| Sr. Scientist, Process Development |
| Experience & Education
9-13 years with Bachelors Degree, 7-11 years with Master's Science, 4-8 years with PhD |
| Morphotek®, Inc. |
Exton |
PA |
9/4/2010
|
| 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.
|
| Teva Pharmaceuticals USA |
Irvine |
CA |
9/4/2010
|
| Sr. Regulatory Compliance Auditor |
|
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Sr. Quality Engineer |
| See above |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Sr. QA GMP Auditor/ Specialist |
| Auditing background, and ability to work/contribute in a team based environment as a lead and an participant, exceptional interpersonal skills, and adept problem solving skills are strongly desired. In addition, the candidate should have willingness to cross train in activities related to GLP and GCP is important. The candidate will also have experience in the creation of standard operating procedures (SOP's).
Three to five years of experience minimum working in a pharmaceutical Quality Assurance environment or related environment
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Sr. Project Manager, IT Technology |
| BS or advanced Education in Information Technology or Computer Science
? Demostrated high level of creativity with respect to utilization of core Project Management practices focused on successful project delivery not the process
? Successfully delivered high visibility projects
? Has strong communication and collaboration skills, successfully resolves conflict
? Has strong leadership skills and demonstrated ability to motivate a global, intra-discipline project team
? Demonstrated ability to work in a weak matrix organization
? Effectively uses Project Management tools to facilitate decision making and enhance communication
? Has a proactive and practical approach to project delivery
? Demonstrated ability to successfully work with vendors
? Understands IT Service-based organizational models, roles and metrics
? Has working knowledge in the area of IT service delivery
? Understands basic concepts of Infrastructure architecture
? Understands concepts and challenges of IT service outsourcing |
| Astellas Pharma, Inc. |
Sacramento (1V060207) |
CA |
9/3/2010
|
| Sr. Professional Representative , Specialty - Sacramento, CA |
| REQUIREMENTS:-3+ years pharmaceutical selling experience including 1 years promoting specialty products -Extensive knowledge of sales processes and pharmaceutical products and industry-Excellent communication, facilitation and presentation skills-Can do approach and very high motivational and persuasion skills-Proven, consistent sales record -A BA/BS degree |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
9/3/2010
|
| Sr. Product Engineer (PVA Platform) |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Sr. Optics/Laser Project Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Sr. NetWeaver Administrator |
| See above |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Sr. Marketing Manager, HCV Marketing |
| - A Bachelor?s degree with a preference for an MBA or advanced degree
- Minimum of 5 years related experience in the pharmaceutical and/or biopharmaceutical arena, including some combination of the following: marketing, sales, or market research. Product launch and/or specialty pharmaceutical experience (especially in HCV/hepatitis) is greatly preferred.
- A strong understanding of the legal and regulatory environment
- An entrepreneurial spirit and ability to develop solutions to complex problems requiring the use of innovation, ingenuity and creativity
- Results oriented and excellent analytic, strategic, business planning, communication and collaboration skills
- The ability to manage complexity and ambiguity in a highly matrixed environment
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Morphotek®, Inc. |
Exton |
PA |
9/4/2010
|
| Sr. Manager/Manager of Project Planning and Informatics |
| Knowledge/Skills/Abilities Required
• Bachelors degree with a minimum of 5 years relevant work experience (Manager) or 8 years of relevant work experience (Sr. Manager)
• At least 3 years experience in Clinical Project Management role, Clinical Informatics role or equivalent position
• Very strong systems / informatics background required
• Very strong organizational and analytical skills required
• MS Project experience strongly preferred |
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Sr. Manager/Associate Director, Labeling & Promotional Compliance |
|
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Sr. Manager, Training and Policy |
Education/Experience Qualified candidates must have a bachelor's degree and a minimum of 7 years of experience in pharmaceutical sales management, marketing management, training, instructional design, policy development or a combination of the above; ability to establish & maintain credibility and trust throughout the organization; strong writing ability and instructional design and training presentation skills; ability to analyze and synthesize information and to draw conclusions; source and manage vendors are critical skills in this role. Familiarity with pharmaceutical company training requirements; familiarity with OIG and trade association guidance documents, prosecutions and CIAs, Sentencing Guidelines and best practices for corporate compliance programs; FDA and pharma experience; sales, marketing, training and policy development experience are also required in this role. Must be willing to travel 20% of the time. |
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Sr. Manager, Regulatory Submission Management |
|
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Sr. Manager, Commercial Compliance |
| ? Thorough understanding of federal and state fraud and abuse laws, including the anti-kickback regulations, the Office of Inspector General reports, and the Food, Drug and Cosmetic Act and understanding of the roles and authority of government agencies and industry cooperative groups including FDA, OIG, and PhRMA
? Extensive experience in managing projects related to commercial pharmaceutical/biotech compliance
? Proven ability to negotiate and partner with others to resolve conflicts
? Ability to handle sensitive, confidential matters and exercise sound discretion and judgment
? Solid project management and interpersonal/communication skills in leading and directing teams to achieve project objectives and goals within assigned timelines
? Demonstrated ability to work independently and manage multiple projects that require collaboration across functional areas
? Team player able to develop rapport and credibility with field and home office personnel including management
? Bachelor?s degree required with at least 5 years pharmaceutical/biotech industry experience in related area of responsibility, legal/regulatory experience a plus.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Sr. Manager, Clinical Studies, Oncology |
| University/College degree with seven years clinical trials experience is desired. Proven time and project management skills, knowledge of drug development process and proven leadership ability is required. Working knowledge of ICH and GCP guidelines is required. Experience in people management is preferred.Proven track record in oncology required. Must have excellent interpersonal, written and verbal communication skills, administrative skills and computer ability. Travel required. |
| Agilent Technologies, Inc. US |
Wilmington |
DE |
9/4/2010
|
| Sr. Manager of Global Marketing - Chemistries |
| Qualifications:
- Bachelor Degree in Business or Sciences or equivalent, MBA preferred.
- 5+ year progressive global marketing management experience including comprehensive experience in benchmarking, market research, advertising, promotions, forecasting and pricing
- Demonstrated ability effectively launching new products and achieving excellent business results.
- Proven success integrating resources across complex functions (sales, marketing, R & D, Supply chain) and across multiple geographies to over-deliver on customer needs. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Sr. Investigator, Global Imaging/MRI |
| The ideal candidate will have a PhD with a minimum of 2-4 years experience (although greater experience is deemed an asset) within industry/academia in the following areas:
- Small animal MRI experience (preferably on Bruker systems) may include multimodality imaging
- Extensive knowledge of imaging application
- Animal skills, such as handling, restraining, anesthesia and injections (IP, IM, IV) in rodents and rabbits.
- Proficiency in data analysis using Excel and statistical software, image processing; computer proficiency (e.g. C++, Matlab, IDL, Linux) is a plus.
- Good inter-personal, communication skills, and working with diverse and talented scientific teams. |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
9/3/2010
|
| Sr. Industrial Designer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Sr. Global Marketing Manager - Tubes |
| See above |
| AstraZeneca Pharmaceuticals |
Westborough |
MA |
9/4/2010
|
| Sr. Financial Analyst |
| Minimum Requirements:
* Bachelor's Degree in Accounting or Finance
* Minimum 8 years of accounting/finance experience of which 5 years are in a manufacturing environment
* Advanced understanding of accounting principles required
* Strong analytical skills with the ability to analyze complex issues and develop recommendations
* Strong Business Partnering skills
* Strong communication, presentation & organizational planning skills required
* Proficiency in PC spreadsheets and database applications
* Previous experience with SAP general ledger and project accounting preferred
* Ability to lead and influence cross functionally
* Demonstrated ability to work in a dynamic work environment
* Strong drive for results
Preferred Background:
* MBA and/or CPA preferred
* Manufacturing experience preferred |
| Astellas Pharma, Inc. |
Washington - East (5DC10403) |
DC |
9/3/2010
|
| Sr. Executive Representative, Hospital - Washington, DC (East) |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Jacksonville (5DA20405) |
FL |
9/3/2010
|
| Sr. Executive Representative, Hospital - Jacksonville, FL |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Novartis Oncology |
na |
CA |
9/4/2010
|
| Sr. Document Controller - Vacaville, CA |
| High school diploma or equivalent
4 years experience in technical word processing or business college certification and 2 years experience. Knowledge of Good Manufacturing Practice (GMPs) required |
| Novartis Oncology |
na |
NC |
9/4/2010
|
| Sr. Director, Operations |
| Skills and Knowledge: Direct experience in Engineering, Manufacturing, QA, Packaging, Production Planning, and Process Development, as well as Logistics and Technical Services; A proven track record of introducing new technology into site operations for continuous improvement in operations, cost management, organizational development, cycle time and capital projects planning and management; Effective team player who possesses strong communication skills. Good communication skills, be articulate and clearly have presence; Mentoring and counseling experience. Team based in thinking with an inclusive management style; Sense of urgency as to objectives, timelines and milestones. Additionally, a contagious make-it-happen approach to the achievement of results; Proven problem solving skills and a roll-up-the-sleeves attitude in working with peers, cohorts and subordinates; Strong financial skills to develop and manage Operations and Facilities budgets; Strong team leadership skills including strong evidence of cross-functional leadership.
?
Education: BA/BS (Technical Emphasis ? Science / Engineering) degree is required; MS or MBA is preferred, but not required. Work Experience: 15 + years of Pharmaceutical Manufacturing experience; Minimum 12 years experience in formulation pharmaceutical manufacturing. Additionally, 10 + years in a senior operations leadership role; Must have demonstrated substantial cGMP knowledge and FDA regulatory inspection experience. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Sr. Director, Global Business Information Management |
| Minimally a BS. Must have 10- 15 years of pharmaceutical industry experience specifically in human drug development, and at least 3-5 years managing a BISM Function globally. Must have a successful track record in the hiring and retention of excellent business interface resources who work optimally in a cross functional team and matrix environment. Must have a successful track record in effectively collaborating with other functions in development, in the development and support of medicines through optimal use of relevant technologies. Must have an in-depth personal experience and understanding of the BISM function, current and future technologies needs and investment and their critical contribution to GDO's successful contribution to drug development. Must also have an understanding of the functions of multiple business units throughout the company, and have maintained effective collaborations with leadership of those business units and functions. Is considered an industry expert and is able to recognize the implications of new directions, trends and developments. Must be a strong and effective strategic thinker and problem solver, requiring the ability to both recognize and anticipate problems, and also help managers and individuals develop their own problem solving skills and discipline. However, must also be able to identify and solve tactical problems and delve into high degree of detail when necessary. Plans for and has detailed knowledge of all available resources internally and externally, has developed the appropriate relationships with partners and vendors, and has the ability to marshal those resources in a productive and efficient manner, either as part of a 3 year strategic capacity plan, or when there is need for sudden and immediate change in direction. |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Sr. Director, Clinical Epidemiology |
| -M.D. or PhD. in Epidemiology required, as well as formal training in epidemiology
8+ years of pharmaceutical pharmacovigilance experience or equivalent in the field of clinical epidemiology
-Solid knowledge of general medicine and clinical practice evidenced by medical training and/or medical practice experience or designing/conducting clinical epidemiological trials.
-Highly evolved understanding of pharmacovigilance guidelines and regulations
-Effectively interacts with Senior Management and integrates activities successfully across the organization
-Excellent verbal and written communication skills
-Strong leadership skills and experience working in a matrix environment
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Daiichi Sankyo, Inc. |
Edison |
NJ |
9/3/2010
|
| Sr. Director, Clinical Development, Oncology |
Education/Experience Qualified candidates must have a MD and a minimum 5 years of pharmaceutical development experience and at least 3 years of hands-on experience managing a major, multi-country, clinical program. Must be an Oncologist. Knowledge of pharmaceutical business, worldwide drug development and regulatory process. Expertise in complex clinical trial design (i.e. factorial design, etc.) and complex implementation (i.e. including Steering Committees, Safety Monitoring Boards, etc.) as well as the interpretation of scientific data. Independent thinking, creativity and innovation. Ability to deliver high quality products. Strong interpersonal skills and ability to interface effectively with multinational development teams in a multicultural working environment. Excellent communication, presentation and negotiation skills with emphasis on building consensus. Ability to effectively manage interactions with academic thought leaders ensuring optimal cooperation for achieving program and department goals. Ability to anticipate and facilitate issue resolution in a multicultural working and business environment. |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Sr. Director Operational Excellence |
Education/Experience Qualified candidates must have a Bachelor’s Degree in Life Sciences, Chemical, Biochemical Engineering or related field; Master’s or Ph.D. preferred. Minimum of 10 years overall work experience with a a minimum of 6 years management experience in the pharmaceutical, biotech or analytical contract laboratory industries. Experience should include process development, manufacturing operations, fill/finish production support, process transfer, scale-up and troubleshooting. Management experience should include Stability, QC, Analytical R&D, direct supervision of technical staff, direction of laboratory operations, and implementation of process and system improvements. Must have strong record of managing and delivering global, cross-functional projects across multiple technologies. Skilled in transitioning support from one team to another. Knowledge of Quality by Design (QBD) and Process Analytic Technology (PAT) and demonstrated ability to apply technology solutions to business problems are required skills in this role. Strong knowledge of regulatory requirements and guidance—particularly cGMPs and a thorough understanding of SAP reporting functionality including standard and organization specific reports are required skills in this role. Active membership with ISPE, RAPS or BIO is highly desirable. Must be willing to travel 15% of the time domestically and internationally. |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Sr. Cost Analyst |
| Minimum Requirements/Preferred Background
* Good working knowledge and understanding of company policies and procedures.
* Demonstrated skills and ability in PC applications (advanced Excel knowledge) and in-depth knowledge of mySAP financial modules and applications.
* Bachelors degree in an accounting or business discipline with a MBA', CPA or CMA preferred. A minimum of 5 years related experience is desired
* Knowledgeable in cost management, strong analytical skills and strong systems' technical skills in order to effectively use PC spreadsheets and data base applications such as Hyperion and mySAP R3 applications.
* Excellent oral and written communications skills required to interact with various areas and management levels, both within and outside of AstraZeneca.
* Excellent interpersonal, organizational and time management skills. |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Sr. Contract Specialist |
| Minimum Requirements
* Bachelor's Degree and 4 years of relevant business experience.
* Excellent attention to detail to ensure successful contract execution that represent a portion of over $6 billion in annual customer discounts.
* Excellent organizational and time management skills with the ability to multitask in order to meet deadlines and provide exceptional internal and external customer support.
* Excellent oral and written communication skills.
* Proficient in Microsoft office applications, specifically Word and Excel, with the ability to adapt and learn query tools and new computer applications.
* Ability to manage daily workload as well as special assignments and projects and deadlines, and serve as a mentor to those at the Contract Specialist level, helping them to prioritize workload and understand individual customer needs and expectations.
* Demonstrated high level of professionalism with the ability to interface with all levels and departments of the organization
Key Leadership Capabilities
* Engages with internal and external customers through communication vehicles to better understand underlying issues/needs and proactively/consistently develops solutions, products or services.
* Ability to think strategically and think broadly, but also identifies opportunities and develops solutions.
* Works collaboratively by respecting and integrating diverse views into decisions/proposals. Works as an individual contributor to accomplish team goals and to support goals of others.
* Drives performance by anticipating and/or removing obstacles for others in order to deliver results and succeed.
* Acts decisively, making effective decisions under pressure and can do so in the absence of complete information.
Preferred Background
* Paralegal Certification from an ABA accredited institution and/or a Bachelor's Degree in a business related field (Finance, Law, Marketing, and/or Health Care).
* 2-3 years previous experience working in Managed Markets or the healthcare industry.
* In-depth knowledge of Pharmaceutical contracting processes
* Proven ability to build/maintain credible and strong relationships with internal/external customers and peers.
* Incumbent should possess a strong understanding of AstraZeneca's product line and competitors, and the various contracting strategies deployed across assigned markets. |
| Novartis Oncology |
na |
CA |
9/4/2010
|
| Sr. Auto & Controls Engineer |
| ? Requires a Bachelors degree in an engineering or related discipline. Equivalent experience may be accepted.
? Requires a minimum of 8 years industry work experience.
? Must be very comfortable with 21 CFR Part 11 and GAMP.
? Must have 5 years experience in a GMP pharmaceutical manufacturing environment or other regulated environment.
? Experience with computer-assisted engineering and design software, CAD and graphics skills are a plus.
? Batch processing and/or filling/packaging controls experience are a must.
? BMS experience is a plus.
? Must possess sound technical judgment and use structured decision-making techniques.
? Good oral and written communication skills are a must.
? Strong computer skills are required.
? Must have an ability to provide technical engineering support in a collaborative, team-oriented project environment.
? Strong project management skills are required.
? Project management skills are a plus. |
| AstraZeneca Pharmaceuticals |
Waltham |
MA |
9/4/2010
|
| Sr. Associate Scientist/Scientist- Biochemist/Enzymologist |
| Minimum Requirements
* Bachelors or Masters degree in biochemistry or enzymology, experience in biochemical assay development in industry or equivalent
* Demonstrated proficiency in data processing or data management
* Demonstrated ability to work in a team-oriented environment
Preferred Background
* Biochemistry, enzymology
* NMR for SAR experience
* Familiarity with automation equipment
* Familiarity with cancer biology and drug discovery
Degree level required and minimum years experience:
* Sr. Associate Scientist: Typically 3 or more years experience post Bachelor's Degree or equivalent
* Scientist: Typically BS/MS with 7 or more years of relevant experience. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Sr. Analyst, IT Quality |
| Bachelor?s Degree in Computer Science, related field, or equivalent experience required.5 + years relevant experience related to change management, document development, and application testing.Working knowledge of computer systems validation processes, system development life cycle, and Change Management processes. Must exhibit creativity and innovation in solutions; be broadly focused and able to manage multiple efforts concurrently.Exceptional attention to details and ability to consistently produce high quality and accurate work.Has solid interpersonal and communications skills (written, oral, and non-verbal) to effectively relate to technical staff and business customers.Ability to be self-directed within the scope of their duties and responsibilities.Ability to build and maintain positive and cooperative working relationships by demonstrating collaborative behaviors and cross functional facilitation skills.Understand the pharmaceutical industry and IT best practices. |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Sr Systems Engineer |
| See above |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Statistical Programmer |
| BA/BS or equivalent experience in mathematics, statistics, computer science or life sciences or related field,
- Fluent in English (oral and written)
Intermediate knowledge of and experience with SAS software.
- Working knowledge of database design/structures.
- Good understanding of global clinical trial practices, procedures, methodologies.
- Good understanding of regulatory requirements relevant to SR (e.g, GCP, ICH).
- Intermediate knowledge of office tools.
- At least 4 years experience in a programming role preferably supporting clinical trials and/or in the pharmaceutical industry (2 years for MS Statistics/Computer Science graduates). |
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Sr Software Engineer |
|
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Sr Scientist, Protein & Toxicology Lab (non PhD role) |
| Minimum Requirements
? Education: Bachelor or Master Degree in Chemistry, Biochemistry, Physiology, Cell Biology, Toxicology or a related Biological Science, with 5+ years of academic or industrial experience in with significant experience in protein mass spectrometry.
? Extensive hands-on experience in the protein biochemistry methods, such as HPLC/Bioplex/gel electrophoresis/cell culture methods etc. Hands-on experience with peptide LC/MS/MS analysis is a great plus.
? Expertise in one or more of the following areas would be an advantage: protein detection assays; functional analysis of proteins in mammalian cells; purification of native and recombinant proteins; protein-protein and protein-ligand binding studies, knowledge of toxicology or cell biology
? Fluency in English (written and spoken).
? Flexibility and ability to work in a team, comfortable with multitasking, good written and oral communication skills, independent and accurate working style, ability to plan and organise effectively, willingness to take on additional responsibilities are expected. |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Sr Scientist, DMPK |
| - Ph.D., or equivalent degree; Post Doctoral Experience is additional qualification.
- 6 - 10 years of Pharmaceutical Industry experience in DMPK
- Experience in GLP regulations, SOPs, interactions with Toxicology, Clinical Pharmacology, Clinical Research, Pharmaceutical Research and Development
- Demonstrated understanding of drug development process within different therapeutic areas
- Good verbal, writing and communication skills and project directed presentation skills
- Working knowledge of drug development process and ICH requirements for drug development
- Established supervisory and ability to operate in a matrix environment
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Sr Scientist, Commercial Support, QbD and CMC |
| * Education and experience related to organic analytical chemistry (Ph.D. degree with three to five years experience or a Masters degree with ten years extensive pharmaceutical industry experience)
* At least 2 years of practical experience in analysis of small organic molecules with HPLC-MS
* Very good team-working skills and the capability to work in a complex environment
* Efficient organization and good documentation skills
* Good command of English; excellent presentation and report writing skills.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Sr Research Scientist |
| Requirements:
* Ph.D., or equivalent degree
* Post Doctoral Experience preferred
* 5 - 10 years of pharmaceutical industry experience in DMPK
* Experience in GLP regulations
* Demonstrated understanding of drug development process within different therapeutic areas
* Excellent verbal, written and communication skills and project-directed presentation skills
* Working knowledge of drug development process and ICH requirements for drug development
* Successful track record of managing staff, and the ability to operate in a matrix environment
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Sr Research Associate |
|
| Astellas Pharma, Inc. |
Bowling Green (1P050205) |
KY |
9/3/2010
|
| Sr Professional Representative- Bowling Green, KY |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Pharmaceutical sales experience highly preferred- Some experience (1 year) with business-to-business sales If you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Jacksonville (1P030205) |
FL |
9/3/2010
|
| Sr Professional Representative, PCP - Jacksonville (South), FL |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Extensive travel is required for this position- Some experience (1 year) with business-to-business sales If you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Yonkers (1P010208) |
NY |
9/3/2010
|
| Sr Professional Representative PCP- Yonkers, NY |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year) with business-to-business sales If you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
San Jose (1P060507) |
CA |
9/3/2010
|
| Sr Professional Representative PCP- Walnut Creek, CA |
| - A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Palm Springs (1P060301) |
CA |
9/3/2010
|
| Sr Professional Representative PCP- Palm Springs, CA |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year) with business-to-business sales If you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Leesburg (1P030304) |
FL |
9/3/2010
|
| Sr Professional Representative PCP- Leesburg, FL |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Las Vegas East (1P060208) |
NV |
9/3/2010
|
| Sr Professional Representative PCP- Las Vegas East, NV |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Harrisburg (1P010609) |
PA |
9/3/2010
|
| Sr Professional Representative PCP- Harrisburg, PA |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Decatur (1P030504) |
GA |
9/3/2010
|
| Sr Professional Representative PCP- Decatur, GA |
| - A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Colorado Springs (1P060106) |
CO |
9/3/2010
|
| Sr Professional Representative PCP- Colorado Springs, CO |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Novartis Oncology |
na |
NE |
9/4/2010
|
| Sr Process Engineer |
| Required: BS degree in an appropriate scientific, pharmaceutical or engineering discipline and atleast 7 to 10 years of demonstrated experience in pharmaceutical formulation, packaging engineering, and/or process development. Experience with pharmaceutical production practices, manufacturing and packaging equipment, and instrumentation and controls. Working knowledge of GxPs. Demonstrated ability to execute facility, process, computerized system, cleaning, and equipment validations.
Preferred: Packaging Engineer or Electrical Engineer with advanced degree. Prior accomplishments in pharmaceutical formulation, development for various dosage forms, or packaging engineering in relevant environments. Prior experience executing capital projects. Working knowledge of analytical testing preferred; demonstrated experience with quality engineering methodology desired.
Only on-line resumes will be accepted. If you require accommodation under the American?s with Disabilities Act to apply for this position,contact Suzanne Drew at (402) 467-8808. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Principal Biostatistician |
| At least Masters Degree in Statistics (or equivalent degree) with 5 years of experience or PhD with 2-3 years of experience.
Fluent English (oral or written)
1. Experience in all tasks of a Trial Statistician.
2. Proven knowledge in Statistics and its applications to clinical trials.
3. Proven knowledge of drug development and HA guidelines. Background medical knowledge, preferably in relation to the specific therapeutic area.
4. Proven knowledge of statistical software packages.
5. Good communication and presentation skills.
6. Good team player. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Sr Pharmaceutical Counsel |
| Key Requirements:
A) Educational
? JD or LLB Degree and admission to the Bar in at least one U.S. state, or an equivalent admission in a relevant foreign jurisdiction
B) Experience
? 10+ years of experience in legal practice
o minimum of 5 years at a law firm required
o experience in management of HR issues, including litigation
o in-house experience preferable
C) Specialized Skills and Knowledge
? Strong knowledge of HR law and issue management, including dispute resolution and litigation
? Clear communication skills, written and oral
? Ability to translate complex legal principles to management
? Demonstrated good ?bed-side manner? in handling sensitive employment issues
? Ability to contribute in a team context
? Strong interpersonal skills in an international environment |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Modeler |
| Master?s Degree in a modeling-related field with a minimum of 5 years of relevant experience, or Ph.D. with a minimum of 2 years of relevant experience, or equivalent degree/expertise. Detailed understanding of molecular & cellular biology, pharmacology, toxicology, physiology and pathophysiology, and/or pharmaceutical R&D process is desirable.
1. Experience in applying either biology, pharmacology or statistics modeling to drug R&D, and exposure to two applied areas out of three at least via collaboration on projects.
2. Good level of knowledge in one or several of the following modeling areas, and knowledge in others: learning algorithms, molecular pathways, biology, tissue effects, physiology and pathophysiology, PK/PD, statistics.
3. Basic-to-good knowledge of the drug R&D process, including clinical development; background medical knowledge and PK/PD knowledge.
4. In-depth knowledge of relevant software packages.
5. Good data exploration skills. Ability to understand heterogeneous data and communicate effectively with people from diverse scientific backgrounds in a multi-disciplinary organization.
6. Exceptional written and verbal communication skills including the ability to interact effectively with a multi-disciplinary team.
7. Good business ethics.
8. Innovative attitude; creative approach to model implementation; welcomes problems as challenges; able to approach problems from multiple angles.
9. Well-developed organizational skills; good project management skills. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Mgr/Assoc Director Product Training |
| ? Bachelor's Degree required
? A minimum of three years of pharmaceutical sales experience required
? 2+ years pharmaceutical training experience strongly preferred
? Oncology experience preferred |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Medical Scientific Expert MD(Thrombosis) |
| MD with unique knowledge for successful clinical program development and execution, with ? 3 years of clinical research experience required.
Or
? MD with specialty with board certification or equivalent required.
Languages:
Fluent English (oral and written)
Experience:
? Advanced medical/scientific writing and communication skills.
? Proven ability to interpret, discuss and represent efficacy and safety data relating to the assigned area.
? Proven ability to work both independently or in a cross functional team setting, including a matrix environment.
? Demonstrated ability to establish effective working relationship with key investigators in assigned TA.
? Medical and/or scientific expertise within a disease area preferred. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Medical Scientific Expert MD(Thrombosis) |
| Strong medical science components to clinical trials/program resulting in high quality analysis of data which enables strategic decisions within the clinical program.
Novartis seen as a credible, ethical and preferred partner by key investigators in the assigned TA.
Education:
? MD with unique knowledge for successful clinical program development and execution, with ? 3 years of clinical research experience required.
Or
? MD with specialty with board certification or equivalent required.
Languages:
Fluent English (oral and written)
Experience:
? Advanced medical/scientific writing and communication skills.
? Proven ability to interpret, discuss and represent efficacy and safety data relating to the assigned area.
? Proven ability to work both independently or in a cross functional team setting, including a matrix environment.
? Demonstrated ability to establish effective working relationship with key investigators in assigned TA.
? Medical and/or scientific expertise within a disease area preferred. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Medical Scientific Expert MD(Metabolism) |
| ? MD with unique knowledge for successful clinical program development and execution, with ? 3 years of clinical research experience required.
Or
? MD with specialty with board certification or equivalent required.
Languages:
Fluent English (oral and written)
Experience:
? Advanced medical/scientific writing and communication skills.
? Proven ability to interpret, discuss and represent efficacy and safety data relating to the assigned area.
? Proven ability to work both independently or in a cross functional team setting, including a matrix environment.
? Demonstrated ability to establish effective working relationship with key investigators in assigned TA.
? Medical and/or scientific expertise within a disease area preferred. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Medical Dir/Executive Medical Director US Medical (Respiratory) |
| An MD, Ph.D., or PharmD (MD is preferred) with a minimum of 2-3 years of Pharmaceutical or equivalent experience, some experience working in US Medcial Affairs, Clinical Research experience related to Respiratory (Allergy Research is ok but less desirable), and in leading other Medical Directors in a Pharmaceutical or equivalent environment is required.
-Ability to orchestrate and synthesize situational analyses (i.e. evidence gap analysis, customer insights, trends in therapy, etc.) across a disease area portfolio of brands to aid in the development of the disease area strategy.
-Integration of portfolio customer & stakeholder strategies with portfolio medical strategies and business drivers.
-Ability to lead in a matrixed environment and influence internal partners to achieve desired business outcomes.
-Ability to communicate effectively, manage issues, resolve conflicts, and mitigate risks.
-Prior strategic leadership experience in pharma or biotech industry.
- Prior line management experience required (3-5 years is preferred).
- Proven proficiency in stakeholder management.
-Proven leadership in clinical strategy development, trial methods, and operations.
-Experienced in presenting scientific data both verbal and written.
-Team building skills
-Understanding of the US market and the stakeholders influencing decisions.
-Advanced business and market knowledge required. Understanding of international regulations applicable to clinical development.
-Basic understanding of biostatistics p values regression correlation Statistical analysis.
-Ability to travel up to 20-25% (some Global) |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Med Scient Expert nonMD |
| MD or PhD with unique knowledge for successful clinical
program development and execution, with 3-5 years of
clinical research experience required.
- Fluent English (oral and written)
- Advanced medical/scientific writing and communication
skills
? Proven ability to interpret, discuss and represent
efficacy
and safety data relating to the assigned area.
? Proven ability to work both independently or in a cross
functional team setting, including a matrix environment.
? Demonstrated ability to establish strong scientific
partnership with key investigators in assigned TA.
? Medical and/or scientific expertise within a disease area
required; Respiratory expertise preferred |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Sr IT Project Manager/ Solutions Delivery |
| Core Project /Practice Management key to success in NIBR IT
? Understands and effectively uses different Project Management approaches
? Understands Adaptive/ Agile Project Management concepts and has used them them in project delivery
? Has strong communication and collaboration skills, successfully resolves conflict
? Has strong leadership skills and demonstrated ability to motivate a global, intra-discipline project team
? Demonstrated ability to work in a weak matrix organization
? Uses collaboration style decision making
? Effectively uses Project Management tools to facilitate decision making and enhance communication
? Has a proactive and practical approach to project delivery
? Demonstrated ability to successfully work with vendors
Technical and domain expertise
? Fully understand systems development lifecycle including configuration and customization of commercial applications (COTS) and their integration into an existing IT environment as well as in house and outsourced software development
? Has working knowledge of one or several phases of systems development lifecycle (educational or experience background in IT solution delivery)
? Understands high level concepts of Systems Architecture in a Research IT/ Pharmaceutical IT setting, including hardware and software systems (understanding of lab automation is a plus)
? Experience implementing IT solutions supporting scientific processes and decision making in Pharmaceutical or Biotech environment |
| Regeneron Pharmaceuticals, Inc. |
Tarrytown |
NY |
9/4/2010
|
| Sr Flow Cytometry Specialist |
|
| Astellas Pharma, Inc. |
Phoenix North (5PP50602) |
AZ |
9/3/2010
|
| Sr Executive Representative Hospital- Phoenix North, AZ |
| REQUIREMENTS:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, Anti-Infective or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
WI (5DC40205) |
Milwaukee |
9/3/2010
|
| Sr Executive Representative Hospital- Milwaukee, WI |
| REQUIREMENTS:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, Anti-Infective or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Biostatistician |
| Education (minimum/desirable): At least Masters Degree in Statistics (or equivalent degree) with 7 years of experience or PhD with 4 years of experience.
Languages: Fluent English (oral and written).
Experience/Professional requirements:
1. Experience gained in the main tasks of program statistician (about 2-4 years).
2. Proven knowledge and expertise in statistics and its applications to clinical trials in at least one TA. Solid experience in drug development process and HA guidelines
3. Background medical knowledge, preferably in relation to the specific therapeutic area.
4..Good knowledge of statistical software packages.
5. Very good project management skills.
6. Very good communication and presentation skills.
7. Ability to give effective guidance to Trial Statisticians and Program Programmers.
8. Good team player. Good business ethics.
9. Good leadership skills. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Biostatistician |
| Typically requires a Master's Degree in Statistics with at least 3 years of related experience. Typical entry level with Ph.D. in Statistics. To be considered for this level, demonstrated proficiency in the following skills and responsibilities are required: With supervision, apply advanced statistical/programming and/or PK/PD modeling in the preparation of CSRs, manuscripts, ISSs, and ISEs that meet world-wide health authority and medical community standards, and participate in protocol preparation. |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Sr Analyst HR Technology SAP Specialist |
Education/Experience Qualified candidates must have a Bachelor's degree in Computer Science, Information Systems, or related field or commensurate experience. A minimum of 3 years experience of HRIS experience including atleast 1 year experience working with reporting in SAP HR - PA, OM, Compensation modules and creating custom queries. Proficiency or experience in PD, LSO, BW, MSS, ESS reporting is a plus. Strong knowledge of HR technology and practices, system technical architecture, office application products database elements, relationship and query concepts/report writing skills; proficient in developing queries; and writing business user specs and possess a strong understanding of relational databases are critical skills in this role. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| SPM/AD, Market Access & Pricing/Distribution Lead: ILARIS Brand Team |
| This person should have strong marketing experience and proven success in the areas of
pricing & reimbursement, managed care, distribution, hub development/management. Specific experience in the development of innovative payer models and distribution a must. Biologic market or other highly specialized drugs is a strong plus. Business and/or biological sciences education with concentration on marketing is preferred (MBA a plus). Sales and sales leadership experience are also highly preferred. Solid strategic thinking skills and analytical skills are essential. Strong senior management communication skills and sales force communication skills are essential.
The applicant must possess a high level of analytical and conceptual ability in order to provide strategic focus to the brand, and demonstrate a proven track record of strong execution and results. The ideal candidate will be proficient at uncovering customer based insights and leveraging this knowledge to drive brand strategy and program development. Additional requirements include the ability to lead and manage teams and multiple vendors. 20% travel is required. |
| Daiichi Sankyo, Inc. |
Worcester |
MA |
9/3/2010
|
| Specialty Sales Representative,Worcester, MA |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Seattle |
WA |
9/3/2010
|
| Specialty Sales Representative, Seattle North, WA |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Manhattan |
NY |
9/3/2010
|
| Specialty Sales Representative, Manhattan North, NY |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Johnstown |
PA |
9/3/2010
|
| Specialty Sales Representative, Johnstown, PA |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Santa Barbara |
CA |
9/3/2010
|
| Specialty Sales Representative - Santa Barbara, CA |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Jacksonville |
FL |
9/3/2010
|
| Specialty Sales Representative - Jacksonville North, FL |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Huntington |
NY |
9/3/2010
|
| Specialty Sales Representative - Huntington, NY |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Albuquerque |
NM |
9/3/2010
|
| Specialty Sales Representative - Albuquerque, NM |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Columbus |
OH |
9/3/2010
|
| Specialty District Manager, Columbus, OH |
Requirements:
BS/BA Degree. Two or more years of Primary Care or Specialty District Management experience. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Specialist III, Accounts Payab |
| Responsible for all aspects of processing vendor invoices, check requests and employee expense reports in accordance with company policy by verifying and completing accounts payable transactions and addressing related issues utilizing professional judgment.
SAP experience strongly desired and manufacturing experience preferred.
5-7 years of related experience
Associates Degree or related experience preferred. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Specialist II, Medicaid |
| Education:
BS or BA Degree preferred. High School Diploma is a minimum requirement for this position. College level credits in Finance, Accounting or Computer related studies will benefit the candidate.
Skills:
Candidate must possess accuracy and speed in data entry. It is essential to be detailed oriented and to have excellent communication skills both written as well as oral. Computer savvy with strong skills in EXCEL, word and adapt to the growing use of the internet for business purposes. SAP knowledge a plus. |
| BD (Becton, Dickinson and Company) |
Holdrege |
NE |
9/3/2010
|
| Specialist - B Shift |
| See above |
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Southwest Regional Director, Medical Science Liaisons |
|
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Sourcing Manager - Learning |
| * Bachelors Degree
* 5 years' work experience
* Minimum of two to three-years procurement experience, strategic sourcing experience is preferred
* Ability to effectively and clearly present information and respond to questions from a wide variety of audiences including groups of senior executives, middle managers and hourly personnel within the company or at supplier/customer engagements.
* Project (sourcing) background in most, if not all, key categories of commercial spend, such as Agency, Media, Market Research, Medical Education, Conferences, Print, Premiums and Direct Marketing is necessary
* Experience with e-procurement is preferred
* Understanding of contract development and business law is required.
* Minimum of two years experience negotiating contracts.
* Proved ability to manage multiple projects/tasks effectively
* Strong written and verbal communication skills
* Proficiency in Microsoft Word, Power Point and Excel
* Demonstrated success working in a team environment
* Strong analytical and organizational skills
* Proficiency in Procurement and other business related systems, e.g. ERP, Ariba
* Financial Analysis, e.g.
- Dun & Bradstreet reports
- Credit Scoring |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Sourcing Manager |
|
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Software Engineer |
| Job Requirements:
? Strong C# programming experience.
? Experience using Microsoft Visual Studio and source management tools, such as Microsoft Team Foundation Server.
? Experience using DevExpress, WPF, or similar GUI toolset.
? Broad knowledge and experience using design patterns.
? Strong work ethic with focus on quality, follow-through, and attention to detail.
? Good communication skills.
? Experience synthesizing a cohesive system consisting of hardware, electronics, firmware, and software.
Education & Experience:
? Degree in computer science, engineering, or related field.
? 5+ years of technical experience.
? Experience developing production quality software.
? Experience with C++ desired.
? Experience with TCP/IP desired.
? Experience with embedded programming desired. |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Software Engineer |
| See above |
| Agilent Technologies, Inc. US |
Loveland |
CO |
9/4/2010
|
| Software Application Engineer |
| Job requirements: This is a key role within an advanced development team. The position requires the following:
? Bachelors or Masters degree in Computer Science or equivalent experience
? Must have at least 4 years technical expertise in SW development processes throughout the development lifecycle (concept to product release)
? Embedded OS & real-time operating systems - WinCE, embedded Linux
? Leadership skills to effectively drive change within R&D teams
? Iterative development techniques - scrum, XP, etc.
? Languages including C++, C#, & Python
? Strong written and verbal communication skills
? Strong collaboration skills with multiple cultures around the world.
Relocation benefits are available |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Small Molecule NMR Scientist (B.S./ M.S.) |
| M.S. or equivalent with 0-5 years or more relevant experience in small molecular NMR with demonstrated success in modern NMR methodologies. Demonstrated skills in data collection and process, spectral interpretation, data management and instrument maintenance are essential. A background in organic chemistry and a keen interest to champion NMR based collaborative research projects with medicinal chemists are required. Proficiency in UNIX/LINUX and expertise in hyphenated NMR technologies are desirable. Excellent communication skills and the ability to multitask in a fast-paced environment are essential. A self-motivated individual as well as a strong team player is required. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Small Molecule Mass Spectrometry Lab Head |
| A Ph.D. scientist with 5+ years of relevant experience or an MS scientist with 10+ years of experience in small molecules MS, structure determination and open access LCMS. In-depth knowledge of mass spectrometry and related techniques and how these can be applied for the analysis of small organic molecules. Expertise in liquid and gas chromatography is expected. Expertise in automation is a plus. Excellent communication skills and the ability to multitask in a fast-paced environment are essential. |
| AstraZeneca Pharmaceuticals |
Waltham |
MA |
9/4/2010
|
| Site Services Facilitator - Waltham |
| Minimum Requirements
* Bachelor's Degree in Engineering or technical related field
* 5 years of contract administration experience in a laboratory or R&D facility
* Proven ability to work effectively in a team environment along with the ability to plan, organize and provide administrative control
* Working knowledge of space management systems
* Demonstrates strong level of oral and written communications skills
* Strong interpersonal skills, creativity and innovation
* Project Management experience
Preferred Background
* Previous Supervisory experience
* Experience working in a LEAN environment
* Knowledge of GXP and FDA Regulations
* Multiple site or cross-functional experience
* Working knowledge of SAP
Leadership Capabilities
* Passion for Customers (Level 2)
* Drives Performance (Level 2)
* Works Collaboratively (Level 2) |
| GE Healthcare |
na |
MD |
9/3/2010
|
| Site Director -Scientific Asset Service Program |
|
* Bachelors degree in Electrical Engineering, Electronic Technology or related technical field; OR Associates Degree in Electronics and 3 years experience servicing electronic equipment in the field
* Previous management of direct reports, leadership, or supervisory experience
* Strong computer competency with solid understanding of Microsoft operating systems (Windows 2000, Windows XP) and Microsoft Office.
* Must be able to lift at least 40 pounds
This position is open to candidates within GE.
GE will only employ those who are legally authorized to work in the United States for this role.
Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
* Bachelor of Science Electrical Engineering Technology with college level courses in Biochemistry/Biology
* Ability to drive organizational change and process improvement
* At least 3 years experience with direct report or leadership responsibilities
* Familiarity with GLP/GMP requirements and/or IQ/OQ.
* Proven ability to develop and execute multiple priorities and approaches to meet objectives and experience in matrix organization
* Field service background and knowledge of Life Sciences market and instruments
* Working knowledge of asset management program
* Excellent communication skills, both written and verbal
* Ability to engage and motivate teams
* Strong verbal and written communication skills
|
| Novartis Oncology |
na |
MA |
9/4/2010
|
| siRNA Chemistry Associate Scientist (BS/MS) |
| ? BS or MS degree in chemistry
? 5+ years of experience in medicinal or
synthetic chemistry
? Is a creative, flexible, open minded, and
curiosity-driven scientist
? Has the ability to work effectively both
independently and with a multidisciplinary
team of medicinal chemists, biologists,
pharmacologists, engineers, and external
collaborators
? Flexibility to work in a fast-paced,
dynamic environment
? Has excellent oral / written
communication and presentation skills |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Sharepoint Developer (VBScript / JavaScript) |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus West |
NE |
9/3/2010
|
| Setup Instruct & Repair - 2nd Shift |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus West |
NE |
9/3/2010
|
| Set-up Instruct and Repair B/D Shift (Reposted liting bidding restrictions for time in Job for Flush Associates) |
| See above |
| BD (Becton, Dickinson and Company) |
Holdrege |
NE |
9/3/2010
|
| Set Up - D Shift |
| See above |
| Agilent Technologies, Inc. US |
Bethlehem |
PA |
9/4/2010
|
| Service Tech Specialist |
| This position requires higher education (Bachelors or Associates degree) or specialized training/certification.
? Requires a minimum of 7 years directly related experience, with typically 9 to 15 years experience
? Expert skills in the calibration and repair of all types of Agilent and Multivendor Test Equipment
? Experience using automated calibration software platforms (STE, PC Based, METCAL, TME etc) is required.
? Requires excellent communication and organizational skills. |
| Agilent Technologies, Inc. US |
Anaheim |
CA |
9/4/2010
|
| Service Tech Specialist |
| This position requires higher education (Bachelors or Associates degree) or specialized training/certification.
? Requires a minimum of 7 years directly related experience, with typically 9 to 15 years experience
? Expert skills in the calibration and repair of all types of Agilent and Multivendor Test Equipment
? Experience using automated calibration software platforms (STE, PC Based, METCAL, TME etc) is required.
? Requires excellent communication and organizational skills. |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
9/3/2010
|
| Senior Systems Analyst |
| See above |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior Statistician Shanghai Chin |
| ?At least Master?s Degree in statistics or a closely related field.
?At least 5 years of experience in drug development (maybe acquired at a CRO) or a related area (2 years for Ph.D.).
?Proven knowledge of drug development and Health Authority guidelines.
?Good command of English, written and spoken.
?Ability to coordinate and oversee a team effort and to give effective guidance to programmers and to less experienced statisticians.
?Work or college experience in another country or demonstrated ability working together in a multicultural organization would be ideal.
?Advanced knowledge of statistical software, in particular SAS. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Senior Software Engineer (BS/MS) |
| The successful candidate will have a Master?s degree in computer science or equivalent experience. Along with a proven track record of building multi-tier, database-backed web applications the candidate should possess:
?Excellent interpersonal and communication skills
?Expert object-oriented programming and Java skills
?Experience with rapid development frameworks such as JBoss Seam
?Experience with Oracle, SQL, PL/SQL, and database design
?Expertise with web application servers
?Experience with Perl, C++, or languages in addition to Java
?Knowledge of Use Case design and UML
?Knowledge of service oriented architectures
?Experience handling ?omix data, especially MS based proteomics data
?At least six years of industry experience preferred |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Senior Software Engineer |
| * Bachelors or Masters degree in computer science and/or physical science.
* More than 5 years experience in industry-related software development
* Experience in the following software fields
- Application development experience using Oracle and SQL databases and Schema Design
- Windows development using .NET, C#, and C++
- Experience with Windows Services, WCF, Web Services
- Experience in server side development
- Desired experience in MVVM & CAL, MSI, MSBuild and WIX
- Also desired are experiences in Search Technologies, Data Object Design and Data Warehousing |
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Senior SharePoint Engineer |
|
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Senior Security Analyst |
| See above |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Senior Scientist/Group Leader, Antibody Generation and Production - Agensys, Santa Monica, CA |
| Ph.D. or equivalent in Immunology, Biochemistry or a related discipline, with at least 8 -10 years of demonstrated experience in a relevant field working either in an academic or bio-pharmaceutical environment. The qualified candidate will have broad experience and knowledge in all aspects of hybridoma or recombinant antibody technologies, including phage display; will be an accomplished investigator with a solid publication or patenting record. Finally the successful individual must be a self-starter, with excellent managerial, communication and interpersonal skills. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior Scientist-Analytical |
| Education:
Minimum: BS/MS or equivalent experience.
Desirable: Advanced degree in a scientific or relevant discipline (Ph.D. or equivalent).
Languages: Fluent English (oral and written)
Experience/Professional Requirement:
1. Minimum of 3 successful years of experience as scientist (promotional pathway) or Ph.D. (0 years experience) or equivalent.
2. Awareness/proven experience for safe handling of chemicals, potentially dangerous materials and equipment.
3. Broad scientific or technical knowledge in a specific area (e.g. synthetic, analytical or galenical).
4. Adequate understanding of development processes.
5. Advanced knowledge in scientific/technical areas of collaboration.
6. Advanced knowledge of laboratory and/or technical tools.
7. Good knowledge of software and computer tools.
8. Good presentation skills and scientific/technical writing skills. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior Scientist-Analytical |
| Education:
Minimum: BS/MS or equivalent experience.
Desirable: Advanced degree in a scientific or relevant discipline (Ph.D. or equivalent).
Languages: Fluent English (oral and written)
Experience/Professional Requirement:
1. Minimum of 3 successful years of experience as scientist (promotional pathway) or Ph.D. (0 years experience) or equivalent.
2. Awareness/proven experience for safe handling of chemicals, potentially dangerous materials and equipment.
3. Broad scientific or technical knowledge in a specific area (e.g. synthetic, analytical or galenical).
4. Adequate understanding of development processes.
5. Advanced knowledge in scientific/technical areas of collaboration.
6. Advanced knowledge of laboratory and/or technical tools.
7. Good knowledge of software and computer tools.
8. Good presentation skills and scientific/technical writing skills. |
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Senior Scientist, Molecular Medicine Imaging |
|
| Morphotek®, Inc. |
Exton |
PA |
9/4/2010
|
| Senior Scientist, Fermentation |
| Knowledge/Skills/Abilities Required
• PhD trained in biochemical engineering sciences or related scientific discipline with minimum of three years of post-doctoral experience in the field of bioreactor fermentation, preferably in an industrial setting
• Extensive hands-on experience in mammalian cell culture process; in-depth working knowledge of stainless steel and disposable fermentors (2L to 250L);
• Must be able to lift at least 50 lbs
• Supervisory skills required
• Good verbal and written communication skills required
• Good interpersonal skills with the ability to work in a team environment required |
| Astellas Pharma, Inc. |
Skokie |
IL |
9/3/2010
|
| Senior Scientist, Bioanalytical Laboratory - Pharmacodynamics |
| Ph.D. in molecular or cellular biology (or equivalent) with 3+ years of related industry experiences, or M.Sc. in science (major in molecular or biological sciences) with 5+ years of related industry experienceKnowledge and experience in molecular/ PCR-based testingKnowledge and experience with immunoassaysKnowledge and experience in biological sample preparationsKnowledge of FDA guideline for bioanalytical method validationWorking knowledge of SOPs and GLP regulatory guidance Ability to transfer and validate biomarkers, immunogenicity and immunoassay methods Knowledge of computer software for laboratory data management Skills in conducting bioanalytical research especially for running clinical samples, documenting data, and assisting report writing following the regulatory requirements.Self-motivated, excellent team player with good communication skills |
| Morphotek®, Inc. |
Exton |
PA |
9/4/2010
|
| Senior Scientist, Antibody Core Development |
| Knowledge/Skills/Abilities Required
• Ph.D., 3 years post-doctoral experience
• Strong background and expertise in molecular biology, recombinant protein or antibody expression and purification (bacterial and mammalian) as well as biochemical and functional characterization of proteins and antibodies is required.
• Familiarity with GS expression systems, FACS analysis, Vector NTI software, Robotics systems/programming, and QPCR light cycler a plus. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Senior Scientist - Molecular Diagnostics |
| The candidate must have a Ph.D. degree in life sciences disciplines (such as Molecular or Cell Biology, Genetics or Biochemistry) with at least 3 years of postdoctoral and at least 5 years diagnostics industry experience.
* Hands-on experience on molecular biology techniques such as nucleic acid sample preparation, PCR, DNA sequencing (including next-generation), real time PCR and mutation detection.
* Familiarity with GLP and GMP environment, documentation and quality system is highly desirable.
*General knowledge with basic statistics analysis tools and understanding DOE and six sigma are also plus.
* Good communication and time management skills. In order to be successful in this position, the candidate should be a good team player in multidisciplinary environment, capable of multi-tasking, able to be fully committed to development timelines, and highly flexible in a dynamic changing environment including format and contents. |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Senior Scientist |
| See above |
| BD (Becton, Dickinson and Company) |
Research Triangle Park |
NC |
9/3/2010
|
| Senior Scientist |
| See above |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Senior Safety Medical Director - Cardiac |
| Requirements --Education and Experience
Given the breadth of roles encompassed by this opportunity, it is recognized that some requirements may be more relevant to certain specific positions and, therefore, the following criteria are intended as guidance:
* Specialty training and board certified/eligible in cardiology/cardiovascular disease
* MD background with strong expertise in cardiology, ideally drug-induced cardiac injury.
* > 5 years of drug development/safety experience the majority of which should be in industry with clear evidence of delivery
* UK physicians will be expected to have completed Higher Medical Training in Pharmaceutical Medicine
* Recognized by peers for therapeutic area expertise and commercial/safety understanding
* Experience in supervising physicians
* Ability to balance business and clinical research objectives
* Experience working with regulatory agencies, preparing regulatory documents and overseeing submissions.
* A thorough knowledge of the pharmaceutical industry, especially clinical research and global regulatory requirements and practices governing expedited and periodic safety reporting, signal generation, safety evaluation and risk management activities
* Proven high quality scientific record
* Demonstrated capability to lead implementation of new technology and/or working routines within a complex organization.
* Excellent verbal and written communication skills.
* Experience in leading of cross-functional teams.
* Broad knowledge of drug development.
Skills and Capabilities
* Strong team-working skills and an ability to work collaboratively in a global pharmaceutical environment
* Strategic thinking
* Strategic influencing
Organizational Behaviors
* Foster behaviors that reinforce AZ as a global organization
* Ensure respect for different practices and expertise in different environments
* Ensure inclusivity of appropriate medical and scientific expertise in strategic and tactical decision-making
* Ensure medical/scientific integrity and commitment to effective communications
Reporting Relationship
* If applicable, this section contains a list of positions that report to the position, either directly or indirectly
* Reports -- none |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Senior Research Associate, Protein Mass Spectrometry- Agensys, Santa Monica, CA |
| Candidate consideration requires a B.S. or M.S. in chemistry, biochemistry or similar field with a minimum of 7 years of laboratory experience. Industrial or academic experience in protein and proteomic analysis by advanced mass spectrometry methods is highly preferred.Hands on experience in protein mass spectrometry method development and experience with Thermo LTQ line of instruments as well as using computational methods for MS data processing are also preferred.The successful candidate will have strong written and oral communication skills, be self-motivated, possess strong organizational skills, and have a track record of working successfully in a team environment. |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Senior Research Associate |
| B.S./M.S. in Biological Sciences/Chemistry or related field with minimum of 4 years of working experience. Hands-on experience with in vitro ADME studies are required as well as experience with design, execution and data interpretation of these in vitro studies. Experience with analytical techniques (HPLC and mass spectrometry) are a plus.
Must be highly motivated, organized with excellent communication skills (both oral and written), detail oriented, and a good team player
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
9/3/2010
|
| Senior Regulatory Compliance Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Senior Quality Engineer - Customer Support |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Senior Quality Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Senior Quality Engineer |
| See above |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Senior Project Manager, DDPM |
| Bachelors Degree required. Advanced degree (masters, doctorate) a plus. Generally, seven (7) years with Masters Degree or ten plus (10+) years relevant experience with a minimum five to seven (5-7) years experience with a demonstrated understanding of the drug development process, and project management skills required. Knowledge of required CMC, pharmacology, toxicology, PK, clinical requirements to support major US regulatory filings ? IND, NDA, etc.Demonstrates clear depth and breadth of understanding of critical early drug development processes Demonstrated expertise /discipline in project management and a key organizer who has shown to set clear priorities on developmental activities, with experience in planning systems (e.g. MSProject) and an understanding of financial planning / expenditures. Good communication, people management and social skills with a good sense of diplomacy both in a scientific and industrial environment.Effectively utilizes information technology systems and provisional project management tools.Capable of managing meetings within a multicultural environment and organize expert meetings with KOLs. |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Senior Project Engineer - Molding |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Senior Project Engineer |
| See above |
| Astellas Pharma, Inc. |
Seattle North (1V060202) |
WA |
9/3/2010
|
| Senior Professional Representative II, Specialty - Seattle North |
| REQUIREMENTS:-3+ years pharmaceutical selling experience including 1 years promoting specialty products -Extensive knowledge of sales processes and pharmaceutical products and industry-Excellent communication, facilitation and presentation skills-Can do approach and very high motivational and persuasion skills-Proven, consistent sales record -A BA/BS degree |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Senior Product Manager / Life Sciences Marketing |
| ? 5+ years of product marketing/management experience; services marketing experience a plus
? Familiarity with Life Sciences industry and analytical instrumentation
? Track record of successful business results
? Bachelors degree in chemistry, biology or related scientific field or equivalent; MBA a plus
? Experience in leading cross-functional and international project teams
? Excellent verbal and communication skills
? Ability to travel, including international, approximately 35% of the time
? Physical work location at a major Agilent site (Santa Clara, CA or Wilmington, DE or Englewood, CO) strongly preferred |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Senior Product Manager |
| ? Minimum bachelors degree in chemistry, biology or related scientific field or equivalent; MBA a plus
? Minimum 4 years of product marketing experience; strong preference for Services Marketing experience
? Minimum of 3 years experience in marketing, selling, commercializing, managing, supporting analytical lab instrumentation or analytical lab experience, preferably in the Life Sciences industry
? Track record of business results
? Strong evidence of customer orientation
? Demonstrated ability to influence all levels of an organization, across regional/cultural boundaries and across multiple disciplines
? Excellent verbal & written communication skills.
? Ability to travel, including international
(10-30%)
Location: In Santa Clara, CA, Wilmington, DE, Englewood, CO |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Senior Principal Scientist |
| As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
At least 7 years experience in Chemical Engineering, Polymer Science, Chemistry or a related technical field. Experience in surface chemistry, controlled release, and polymer chemistry is desired. Experience in a regulated (GxP) environment is preferred. The ideal candidate will also have experience in the scale-up and transfer to manufacturing of chemical processes, pharmaceuticals, or medical devices
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Senior PhD Scientist: Protein Purification and Expression |
| The Lab Leader of protein expression and purification group will possess the following qualifications:
?PhD with a minimum of five years of research in protein expression, purification, biochemistry or closely related discipline.
?General knowledge of state-of-the art technologies, platforms and approaches which enable practical yet innovative ways to support drug discovery programs.
?Thorough understanding of protein chemistry, biochemistry, bacterial, yeast and mammalian expression systems for tool generation to ensure the success of target-driven drug discovery.
?Strong command of academic or commercial research efforts and of scientific literature, and knowledge of key opinion leaders in the area.
The Leader of protein group will be a decisive and results-oriented individual who is flexible, team-oriented, creative and able to excel in a multi-project, fast-track environment. He or she will be a strategic thinker who interacts and collaborates with project teams, peers and management in identifying and achieving discovery goals from both scientific and strategic perspectives. |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
9/3/2010
|
| Senior Molding Engineer |
| See above |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Senior Medical Writing Program Manager, Oncology |
| BA/BS degree or equivalent; 10+ years relevant experience. Preferred: MS/MA/MPH with at least 7 years as a writing professional in pharmaceutical industry.Activities require expert technical skill (e.g., as defined by Drug Information Association Medical Writing Competency Model) including techniques of scientific writing and editing; ability to interpret and communicate clinical and numerical data, and verify consistency in data; comprehend and communicate scientific concepts; interpret and communicate clinical, nonclinical, biopharmaceutic, pharmacology, ADME and CMC data and information.Activities require advanced document and process experience, and highly complex problem solving/issue resolution to achieve corporate objective(s), resourcefulness and sharing of expertise.Technical expert for the majority of document types produced by medical writing. Demonstrated and substantial experience in managing the creation of IND/IMPD or NDA/MAA components, briefing documents and white papers. |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Senior Medical Information Manager |
| Qualifications:
* Advanced degree in Pharmacy (PharmD preferred), Pharmacology, Science or equivalent clinical experience
* Pharmacy Licensure preferred
* 2+ years experience in pharmaceutical industry based Drug Information Delivery or equivalent industry experience
* Demonstrated expertise in drug information communication and management
* Excellent oral and written communication skills and interpersonal skills
* Knowledge of FDA requirements
* Ability to apply Regulatory and Compliance guidelines to Drug Information delivery
* Understanding of the information needs for various customer segments
* Project Management leadership experience
* Strong leadership ability
Preferred Background
* Clinical Pharmacy experience with patient care exposure
* Drug Information Residency or equivalent experience
Skills and Competencies
* Expert Scientific Knowledge
* Leadership Skills
* Drug Information Management Expertise
* Regulatory and Compliance Expertise
* Organization Savvy
* Communication Skills
* Presentation, Facilitation and Instructional Skills |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Senior Medical Director, CF |
| · MD, DO or international equivalent
· Minimum of 5 years pharmaceutical industry experience, including time managing clinical trials and/or clinical development program(s)
· Preferred qualifications include sub-specialty training in internal medicine, family practice, pediatrics, pulmonary medicine, allergy, and/or industry background
· Board certification/eligibility in specialty area
· Ability to work collaboratively in a challenging team matrix environment
· Ability to work independently to resolve challenges and conflicts
· Possess a comprehensive understanding of applicable US and EU regulatory requirements and of the drug development process
· Have a working knowledge of biostatistics, data management, clinical operations and clinical pharmacokinetic scientific and technical processes
· Experience in filing and defending US INDs and/or NDAs
· Excellent communication skills
· Willing to re-locate to the Cambridge area
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Optimer Pharmaceuticals Inc, Inc |
San Diego |
CA |
9/4/2010
|
| Senior Medical Director of Pharmacovigilance |
| Educational/Experience Requirements
•MD degree with a minimum of five years industry experience in drug safety surveillance and pharmacovigilance.
•Experience in development of risk management plans is essential.
•Knowledge of global pharmaceutical regulations and guidances highly desirable.
•Clinical experience and sound medical judgment,
•Excellent analytical skills and the ability to both write and review medical reports.
•Excellent written and oral communication skills.
•Excellent interpersonal, organizational, and team-building skills.
Interested candidates e-mail resume and include job title in subject line to:
careers@optimerpharma.com
About Optimer Pharmaceuticals
Optimer Pharmaceuticals, Inc. is a biopharmaceutical company focused on discovering, developing and commercializing innovative anti-infective products to treat serious infections and address unmet medical needs. Optimer has two late-stage anti-infective product candidates under development. Fidaxomicin, formerly known as OPT-80, is the only antibiotic therapy currently in Phase 3 worldwide clinical development for Clostridium difficile infection. Pruvel™ (prulifloxacin) is an antibiotic which has completed two Phase 3 clinical trials for the treatment of infectious diarrhea in travelers. Additional information can be found at http://www.optimerpharma.com
|
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
9/3/2010
|
| Senior Mechanical Engineer |
| See above |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Senior Marketing Director |
| Minimum Education Requirements:
Degree in Business Admin. Marketing ? MBA desired
Minimum Experience Requirements:
8-10 Yrs. Experience in Marketing in the Life Science, FMCG?s industries
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| SENIOR MANUFACTURING SUPPORT ENGINEER |
| See above |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Senior Manager, Government Pricing & Analytics |
| Minimum Requirements
*Bachelor's Degree
*Minimum of 7 years experience in pharmaceutical or healthcare industry, public or private contracting, or consulting; 2 years direct people management experience.
*Strong knowledge of pharmaceutical contracting, pricing, marketing/sales, or finance.
*Demonstrated abilities to influence without authority, lead teams and develop/foster relationships with senior leadership.
*Strong communication (oral & written) and analytical skills with excellent attention to detail.
*Ability to manage multiple priorities and strong organization skills.
Skills and Competencies
*Knowledge of Government and Medicaid contracting and claims/discount processes.
*Ability to think strategically and broadly, using this insight to challenge and adapt current approaches / ways of doing things.
*Works collaboratively by respecting and integrating diverse views.
*Drives performance by anticipating and/or removing obstacles for others in order to deliver results and succeed.
*Acts decisively and makes effective decisions and can do so in the absence of complete information and when under pressure.
*Thorough understanding of the AstraZeneca product line, key government reporting requirements and the various contracting strategies deployed across markets.
*Skilled in utilizing information technology and systems, working with spreadsheets, databases, and decision support and query tools, specifically Excel and MS Word
Preferred Background
*MBA
*An educational or professional background in Government and/or Medicaid systems or finance.
Internal and External Contacts/Customers
*Account Directors
*Contracting Directors
*Strategy Managers
*Legal
*Finance
*Information Systems
*State & Government Affairs
*Brand Teams
*AstraZeneca contracted customers, specifically Federal and State Government Agencies
*Outside legal counsel
*Outside industry experts
Reporting Relationship
*Direct Reports -- 1 Govt Pricing Manager and 3 Govt Pricing Analysts
*Indirect Reports - N/A |
| Millennium Pharmaceuticals |
Albany |
NY |
9/3/2010
|
| Senior Manager, Global Medical Affairs Outreach |
|
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Senior Manager, Clinical Studies |
| University/College degree with seven years clinical trials experience is desired. Proven time and project management skills, knowledge of drug development process and proven leadership ability is required. Working knowledge of ICH and GCP guidelines is required. Experience in people management is preferred. Must have excellent interpersonal, written and verbal communication skills, administrative skills and computer ability. Travel required. |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Senior Manager, Clinical Programs |
| See above |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Senior Maintenance Mechanic - Agensys, Santa Monica, CA |
| ? A High School Diploma? Ten years relevant experience in Bio-Pharmaceutical, petrochemical, packaging or power generation industries with at least four years of that in a pharmaceutical FDA regulated GMP environment ? Demonstrated abilities and /or evidence of training in the repair, operations and troubleshooting of electromechanical process equipment, HVAC systems and utility systems? The ability to read blueprints and P&ID?s? Good communication skills verbal and written? Good computer and keyboard skills, proficient with standard business software |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior Investigator, Clinical PK/PD |
| Minimum Requirements:
Ph.D./Pharm.D. level scientist with 3 years of relevant experience, or Masters Level with at least 5 years relevant experience.
At least 3 years experience in drug development or a relevant environment (e.g. Clinical Pharmacology or Drug Metabolism and Pharmacokinetics).
Proven knowledge of PK and PK/PD evaluation techniques.
Experience of working in project teams (preferably global) and sound awareness of recent developments in drug development sciences essential.
Knowledge of regulatory requirements and experience in dealing with regulatory authorities. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior Investigator, Clinical PK/PD |
| Ph.D./Pharm.D. level scientist with 3 years of relevant experience, or Masters Level with at least 5 years relevant experience.
At least 3 years experience in drug development or a relevant environment (e.g. Clinical Pharmacology or Drug Metabolism and Pharmacokinetics).
Proven knowledge of PK and PK/PD evaluation techniques.
Experience of working in project teams (preferably global) and sound awareness of recent developments in drug development sciences essential.
Knowledge of regulatory requirements and experience in dealing with regulatory authorities. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Senior Global Buyer |
| List Minimum education, training and experience needed to perform this job:
1. Minimum 4-year degree required (or equivalent)
2. Proficiency in ERP/e-procurement systems required. (Will train in ERP systems for right candidate.)
3. 3-5 years experience in procurement industry, supply chain management (SCM) required (for new college graduate ? courses or focus in Procurement / SCM required)
4. Strong interpersonal and teamwork skills
5. Able to make decisions based on quantitative data required |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Senior Formulation Development Scientist |
| - A degree in pharmaceutical sciences, chemistry, chemical engineering, materials science or related field
- PhD (or equivalent degree) and 4+ years of productive, relevant work or postdoctoral experience
- M.Sc. (or equivalent degree) and 7+ years of productive, relevant work experience.
- B.Sc. (or equivalent degree) and 10+ years of productive, relevant work experience.
- Proven ability to apply the principles of the basic sciences such as physical and organic chemistry, thermodynamics, and materials science, to formulation and process development, using a rational, scientific approach.
- Demonstrated ability to develop solutions to complex problems with creativity and innovation
- Formulation development experience on solid oral dosage forms is preferred, especially experience with small molecule NCEs and poorly soluble compounds
- Experience with a range of dosage forms, including liquids, solids and oral, iv formulations, controlled release and pediatric applications would be advantageous
- Expertise in process scale-up and optimization from laboratory scale to pilot scale and registration scale as well as familiarity with engineering scale-up principles, i.e., dimensional analysis.
- Experience applying statistical approaches in the design and analysis of experiments would be advantageous
- Experience working with and managing interactions with contract manufacturing vendors
- Inventive and innovative, self-starter who is comfortable and successful working in a multi-disciplinary team under defined timelines
- Proven teamwork, leadership and collaboration skills, with a demonstrated ability to interact and influence manage all levels of business
- Excellent verbal and written communication skills
- Demonstrated strategic planning, and organizational skills
- Supervisory experience would be a plus but not necessary
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| BD (Becton, Dickinson and Company) |
Research Triangle Park |
NC |
9/3/2010
|
| Senior Engineer- Electrical/Systems |
| See above |
| BD (Becton, Dickinson and Company) |
Research Triangle Park |
NC |
9/3/2010
|
| Senior Engineer - Process/Project |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Senior Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Waltham |
MA |
9/3/2010
|
| Senior Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Waltham |
MA |
9/3/2010
|
| Senior Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Senior Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Senior Engineer |
| See above |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Senior Director, Statistics & Clinical Programming |
| Minimally a PhD in Statistics, or equivalent Degree, with specialization in Pharmaceutical Drug Development or equivalent work experience. Must have at least 10-15 years of pharmaceutical industry experience specifically in human drug development, and at least 3-5 years managing managers within a biometrics, biostatics function in clinical development. Preferably, will have successfully led a global Biostatistics and Programming function in a major pharmaceutical company. Must have a successful track record in the hiring and retention of excellent statistical and data management scientists who work optimally in a cross functional team and matrix environment. Must have a successful track record in effectively collaborating with other functions in development, discovery research, Medical Affairs and Commercial in the development and support of medicines. Must have an in-depth personal experience and understanding of the relevant expert groups within the Statistics and Programming function and their critical contribution to drug development. Must also have an understanding of the functions of multiple business units throughout the company, and have maintained effective collaborations with leadership of those business units and functions. Is considered an industry expert and is able to recognize the implications of new directions, trends and developments in the area of design, acquisition and reporting of data in the pharmaceutical industry. Must have extensive knowledge of the application of statistical analysis and reporting tools. Must be a strong and effective strategic thinker and problem solver, requiring the ability to both recognize and anticipate problems, and also help managers and individuals develop their own problem solving skills and discipline. However, must also be able to identify and solve tactical problems and delve into high degree of detail when necessary. Plans for and has detailed knowledge of all available resources internally and externally, has developed the appropriate relationships with partners and vendors, and has the ability to marshal those resources in a productive and efficient manner, either as part of a 3 year strategic capacity plan, or when there is need for sudden and immediate change in direction.Displays the highest level of personal commitment to the Astellas code of Ethics. Is exemplary in ensuring that "every employee deserves a great manager". Inspires while holds all appropriately accountable. Commits through co-accountability, to the growth and health of GDO, APGD and Astellas. |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Senior Director, Safety Operations |
| - M.D. or Masters /Doctorate level in life sciences or allied health fields preferred; Bachelor degree in life sciences or allied health fields required; 8+ years of direct Pharmacovigilance experience
- Solid knowledge of safety database operations and function
- Strong knowledge of Global Regulations, standards and best practices regarding safety processing and reporting, safety surveillance and pharmaceutical industry compliance activities in pre-marketing and post-marketing
-Strong operational skills as demonstrated by leading previous projects or functions and or equivalent in training and education in areas such as lean sigma or MBA
- Excellent verbal and written communication skills.
- Self-starter with proven ability to thrive in a fast-paced environment handling multiple simultaneous high priority tasks
- Successful track record of developing and mentoring staff
- Maintains high ethical standards, including a commitment to Vertex's values and behaviors
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Senior Director, IT Client Relationship Management |
| Serves as the IT liaison for a specific enterprise wide business unitManages the IT resources dedicated to the business unit or functionWorks directly with the senior leadership of the business unit and IT Performs or directs high level activities with appropriate awareness of other activities within the organizationServes as a business advocate to IT and an IT advocate to the businessResolves complex business issues that affect cross functional areas or multiple sitesDirects the IT application and support requirements from a staffing perspectiveKeeps the Business and IT informed of important changes in each of the respective areas Leads complex business process reengineering projects Controls project priorities and ensures balance between business needs and IT resource constraintsResponsible for project delivery, providing ongoing updates and advocacy to the Business and IT Meets regularly with business personnel to define, review or revise:IT support strategiesApplication portfolioProject priorities and statusSystems supportApplications and infrastructure service levelsApplication growth projections and new access requirementsDirects the development and documentation of IT Strategies and Plans as a member of the IT Senior Management TeamWorking jointly with key business contact(s), manages the IT budgets, projects and prioritiesExtensive knowledge and skill through broad and/or deep experiences in Pharma IT Strong communication and interpersonal skills, capable of motivating and influencing teamsPerform at the highest levels and able to make decisions on their ownAble to translate between technical and business leaders at the highest levelsViewed as credible, and well respected by the business and IT organizationsAccountability in building and maintaining positive and cooperative working relationships Fifteen or more years of relevant experience within the pharmaceutical industry Collaboration and cross functional facilitation skillsHigh level understanding of project management, quality assurance, and IT best practicesProficiency with commercial applications that are designed to support enterprise wide business capabilitiesAdvanced Degree required (or progress towards and significant industry experience) |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Senior Director, Global PK Modeling & Simulation |
| PhD in Life Sciences required. Must have at least 10 or more years of pharmaceutical industry experience, specifically in global human drug development, both in exploratory development, late clinical pharmacology and later phases of development. Broad therapeutic area knowledge and prior experience with biologicals is important. Extensive knowledge experience in application of PKMS in global drug development, both in Exploratory Development as wel as late CP. Good understanding of Late Development as well as Drug Discovery.Good knowledge of mathematics and power of mathematical modelsMust have a successful track record in interactions with Global Regulatory authorities; prior experience contributing to successful regulatory filings highly important. Must have a successful track record in the hiring and retention of excellent scientists who work optimally in a cross functional team and matrix environment. Must have a successful track record in effectively collaborating with other functions in development, discovery research, Medical Affairs and Commercial in the development and support of medicines. Displays the highest level of personal commitment to the Astellas code of Ethics. Is exemplary in ensuring that "every employee deserves a great manager". Inspires while holds all appropriately accountable. Commits through co-accountability, to the growth and health of GCPED, APGD and Astellas.Must have an in-depth personal experience and understanding of the GCPED function and its critical contribution to drug development. Must have extensive experience in interactions with global Regulatory Authorities. Must also have an understanding of the functions of multiple business units throughout the company, and have maintained effective collaborations with leadership of those business units and functions. Is considered an industry expert and is able to recognize the implications of new directions, trends and developments as it relates to GCPED and Astellas business. Must be a strong and effective strategic thinker and problem solver, requiring the ability to both recognize and anticipate problems, and also help managers and individuals develop their own problem solving skills and discipline. However, must also be able to identify and solve tactical problems and delve into high degree of detail when necessary. Plans for and has detailed knowledge of all available resources internally and externally, has developed the appropriate relationships with partners and vendors, and has the ability to marshal those resources in a productive and efficient manner, either as part of a 1-3 year strategic capacity plan, or when there is need for sudden and immediate change in direction. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Senior Director, Clinical Study Management |
| Minimally a BS. Must have at least 10 years of pharmaceutical industry experience specifically in human drug development, and at least 3-5 years managing managers of Clinical Study Managers in multiple therapeutic and geographic areas. Must have a successful track record in the hiring and retention of excellent clinical operations resources globally, who work optimally in a cross functional team and matrix environment. Must have a successful track record in effectively collaborating with other development functions in the development and support of medicines. Must have an in-depth personal experience and understanding of the Clinical Science function and the critical contribution of Clinical Operations to drug development, Must also have an understanding of the functions of multiple business units throughout the company, and have maintained effective collaborations with leadership of those business units and functions. Is considered an industry expert and is able to recognize the implications of new directions, trends and developments globally and on a multi-country and regional level, in site and patient recruitment, site monitoring, essential document collection and management, and the optimal use of cross functional outsourcing relationships. Must be a strong and effective strategic thinker and problem solver, requiring the ability to both recognize and anticipate problems, and also help managers and individuals develop their own problem solving skills and discipline. However, must also be able to identify and solve tactical problems and delve into high degree of detail when necessary. Plans for and has detailed knowledge of all available resources internally and externally, has developed the appropriate relationships with partners and vendors, and has the ability to marshal those resources in a productive and efficient manner, either as part of a 3 year strategic capacity plan, or when there is need for sudden and immediate change in direction. |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Senior Director Clinical Research-Alzheimer's Disease |
| Requirements --Education and Experience
o Medical doctor with specialty training and board certification in adult neurology with significant experience in Alzheimer's drug development (PhD candidates with extensive clinical experience may also be considered).
o Experience in clinical and preclinical science in Alzheimers disease.
o Greater than 5 years of drug development /commercialization experience (the majority of which should be in industry) with clear evidence of delivery
o Ability to balance business and clinical research objectives is critical
o Thorough understanding of pharmaceutical safety reporting and surveillance processes
o Experience working with regulatory agencies and preparing regulatory documents
Skills and Capabilities
o Strong team-working skills and an ability to work in a global pharmaceutical environment
o Strategic thinking
o Strategic influencing
Organizational Behaviors
o Foster behaviours that reinforce AZ as a global organization
o Ensure respect for different practices and expertise in different environments
Leadership Capabilities
o Passion for Customers
o Thinks Strategically
o Acts Decisively
o Drives Performance
o Works Collaboratively
o Develops People and Organization |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior Data Manager |
| Education: Bachelors degree in life sciences, computer science, pharmacy, nursing or equivalent relevant degrees.
Languages: Fluent English (oral and written)
Experience/ Professional Requirements:
1) Ideally 5 or more years experience in drug development with at least 4 years in Data Management activities.
2) Project team leadership experience required.
3) Good technical and problem solving skills.
4) Thorough understanding of clinical trial methodology GCP and medical technology.
5) Ability to work independently, under pressure demonstrating initiative and flexibility.
6) Attention to detail and quality focused.
7) Good organization planning and project management skills.
8) Good interpersonal and communication skills and ability to operate effectively in an international environment.
9) Good negotiation skills.
10) Thorough understanding of physiology, pharmacology, clinical study objectives and the drug development process.
11) Ability to mentor, coach within Data Management and cross functionally and train internal and external partners. |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Senior Counsel - Managed Markets |
| * Law degree
* Professional legal qualification
* Significant legal practice experience, preferably in pharmaceutical or other regulated industry
* AstraZeneca leadership capabilities at Level 3
* Recognized expertise in law relevant to Managed Markets including government pricing
* Strong proficiency in relevant legal practices
* Strong interpersonal and communication skills
* Proven skills in analyzing and solving issues related to Managed Markets
* Proven ability to work as part of a cross-functional team |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Senior Compensation Specialist |
| ? Bachelors Degree in Business Administration, Accounting, Finance or related field
? Must have a minimum of 5 yrs of compensation experience; pharmaceutical industry experience preferred
? Excellent analytical skills including the ability to analyze a variety of data, determine validity, draw conclusions & make recommendations
? Advanced proficiency of Microsoft Excel
? Proficiency with Microsoft Word & Power Point
? Experience working with HRIS (Peoplesoft, Oracle, SAP, SuccessFactors) preferred
Other Skills and Abilities:
? Excellent organizational skills and attention to detail
? Excellent communication skills
? Flexible, adaptable and open to change
? Use of good judgment
? Well developed analytical and problem solving skills
? Works harmoniously and effectively with others as part of a team
? A self-starter who desires to show ownership and commitment to the job
? Exercises confidentiality and discretion
? Action oriented, with a focus on continuous improvement; also high energy with a challenging but positive style.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Senior Clinical Trial Associate |
| See above |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Senior Clinical Staffing Consultant |
| ? 5+ years pharmaceutical clinical or medical recruiting experience a must, minimum of a Bachelors degree or equivalent
? Experience working in a fast-paced, highly matrix organization
? Proven track record of finding unique ways to source and attract qualified candidates
? Superior selection skills and a high level of proficiency in assessing individuals
? Proven ability cultivating successful relationships internally and externally
? Results driven, ability to demonstrate/quantify success relative to established targets and metrics
? Strong listening, facilitation and communications skills
? Strong organizational, multi-tasking and computer and web skills, along with the ability to handle sensitive and confidential situations/information
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Morphotek®, Inc. |
Exton |
PA |
9/4/2010
|
| 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%
|
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Senior Clinical Pharmacologist |
| * PharmD or Ph.D. and 2-5 years of industry experience
* NCE drug development experience with at least 5 NCEs in the past
* Possesses good knowledge of drug Development Programs and a keen awareness of development issues
* Able to integrate the activities of distinct functional groups across multiple projects
* Can recognize and carry out productive new development initiatives/directions Is a mid-level experienced mentor who effectively infuses confidence and team commitment: can make clear written and oral presentations.
* Exhibits a record of excellent operational and ethical standards, and team-improvement
* Demonstrated ability to provide career development to staff
* Able to recognize and resolve important organizational problems and/or infusing innovation Has leadership abilities, can initiate and carry out tasks with little direct supervision
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Regeneron Pharmaceuticals, Inc. |
Tarrytown |
NY |
9/4/2010
|
| Senior Buyer- Indirect Services |
| 'Bachelor's or Master's degree or equivalent work experience required; C.P.M. or C.P.M.S. required
'5-8 years progressive experience in Procurement with an emphasis on Information Technology and Facilities
'Experience working in/with Pharma/Biotech companies required (mid-sized Biotech strongly preferred)
'Robust project management support for multiple projects to ensure the successful completion of specific project goals and objectives are met within budget and on time, i.e. IT projects, new building requirements
'Demonstrated ability to drive results in an expedient manner quickly gathering information and consensus along with making sound decisions
'Translates business objectives into actionable priorities
'Ability to perform with minimal supervision
'Demonstrated ability to support internal clients and lead
'Competent in effectively communicating, both verbally and in writing within all levels of the organization
'Demonstrated ability to think and act strategically
'Proven experience in negotiating, reviewing and managing client requirements; contracts; policies and procedures
'Extensive experience in negotiating agreements for the organization, i.e. Contract/Pricing Agreements such as waste management; uniforms
'Vendor/Partner relationship management
'Demonstrated ability to work well with people from many different disciplines
'Oracle or similar ERP solution experience preferred
'Expert in the use of Microsoft Office suite (Word, Excel, Power Point,Visio) and MS Outlook
|
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Senior Business Partner ? Learning and BDU |
| See above |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Senior Business Analyst/Project Manager |
| Qualified applicants will have a Bachelor?s degree in Computer Science or Management Information Systems and a minimum 10 years experience as a Project Manager working in an Information Systems group (preferably within the Pharmaceutical of Life Sciences industry). PMP certification preferred.
Experience with Oracle E-business Suite (Oracle Project Accounting, Accounts Payables, General Ledger, Cash Management, Fixed Assets, iProcurement, Purchasing, Order Management, Accounts Receivables, Alerts, Approvals Management Engine (AME), and Application Desktop Integrator (ADI)). MicroStrategy, Kaplan, Concur, Hyperion, Cognos, Noetix, Kenexa , iManage, KBX, Ceridian and Outlooksoft is a plus.
Skills and capabilities:
* Strong project, program and portfolio management skills
* Strong leadership and team facilitation skills
* Strong business and process analysis skills
* Strong knowledge of industry solutions and best practices
* Strong communication and presentation skills
* Strong conflict management skills
* Strong negotiation and influencing skills
* Strong networking skills
* Strong time and meetings management skills
* Interpersonal, facilitative, consultative, responsive
* PC skills include: MS Project, MS Visio, MS Office
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Senior Business Analyst, Bioinformatics |
| Qualifications:
? Idea candidate should have an advanced degree in biology and/or B.S in Computer Science
? At least 3-5 years experience in a scientific or biotech environment
? Strong communications and interpersonal skills
? Proven capabilities interacting with scientists and being customer service oriented
? Ability to work independently and/or as part of a team
? Extensive knowledge in the biology, working experience related to the drug metabolism and pharmacokinetics research process will be strong plus
? Good understanding and practical experience in data management and data analysis tools to support research process
? Solid understanding of relational databases and familiarity with Oracle and/or SQL server
? Strong software engineer knowledge and extensive practical experience |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior Brand Manager-Prevacid |
| ? MBA
? 5+ years of consumer packaged goods marketing experience. Prior experience in healthcare industry and knowledge of regulatory issues impacting the industry preferred.
? Broad knowledge of healthcare and OTC industry, markets, and competitive products, new business development experience. Broad knowledge of market research data sources and applications. OTC product launches or switch experience.
? Creative problem solving skills
? Excellent analytical skills
? Strong leadership skills particularly of cross-functional teams
? Strategic thinking potential and proactive self-starter
? Significant knowledge of sales and marketing techniques, market research data sources and applications, is required.
? Personal computer efficiency required (Word, Excel, PowerPoint, Lotus Notes preferred).
? Well-developed oral, written and analytical skills.
? Requires significant amount of innovation and creativity to champion profitable products to market quickly. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior Brand Manager |
| - Creative problem solving skills
- Excellent analytical skills - - Stong leadership skills particularly of cross-functional teams
- Strategic thinking potential and proactive self-starter.
- Significant knowledge of sales and marketing techniques, market research data sources and applications, is required.
- High efficiency with Word, Excel, PowerPoint, Lotus notes prefer.
- MBA (Marketing concentration) preferred.
- Must have 5+ years of consumer packaged goods marketing experience.
- Well-developed communication skills
Preferred:
- Knowledge of regulatory issues impacting the industry
- Broad knowledge of healthcare and OTC industry, markets, and competitive products, new business development experience.
- Knowledge of market research data sources and applications. OTC product launches or switch experience. |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Senior Auditor |
Education/Experience Qualified candidates must have Bachelors degree with 3 or more years auditing experience in GAAP/auditing and accounting principles. Focus in internal controls and fraud prevention is preferred. Knowledge of business processes and internal controls and experience auditing those processes for control weaknesses and reliable financial reporting; and experience conducting interviews of employees/vendors/customers is preferred. Demonstrated abilities and competencies in Sarbanes Oxley and/or J-SOX; COSO Integrated Control Framework; PCAOB Auditing Standards; IIA’s International Standards for the Professional Practice of Internal Auditing; SAS 99; and Generally Accepted Accounting Principles (GAAP) is also required. CPA or CFE and Public Accounting Experience is preferred. Must be willing to travel 15% of the time. |
| AstraZeneca Pharmaceuticals |
Waltham |
MA |
9/4/2010
|
| Senior Associate Scientist/Associate Scientist |
| Minimum Requirements
BS in microbiology or relevant discipline.
Skills and Competencies
*Aseptic microbiological techniques
*Operation and troubleshooting of robots.
*Handling and managing large volumes of samples and data.
*Proficient with PC-based software.
*Effective communication and collaboration skills.
*Able to work with people from other disciplines and backgrounds.
*Flexibility.
*Concern for standards.
Preferred Background
*Experience in susceptibility testing of antibacterials.
*Experience in industrial setting.
*Strong work ethic.
*Experience in microbiological assay development. |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Senior Analyst Marketing Research |
Education/Experience Qualified candidates must have a Bachelor degree; MBA degree is desirable. Minimum of 4 years of pharmaceutical experience; and 3 years of marketing research experience is also required. Ability to proficiently use Microsoft Office tools; read, analyze, and incorporate secondary data; and analyze data tabulations are critical skills in this role. |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Senior Analyst Field Analytics |
| Education/Experience: Qualified candidates will have a Bachelor's Degree; preferably in Business Administration, Quantitative Methods, Market Research, Information Management or a related field. MBA is preferred. Candidates should have 3-5 years of experience, preferably in a Sales Operations function in the pharmaceutical industry, and 3-4 years of experience that should include report development and sales analytics. Must have systems experience with 2 of 4 of the following: decision support, data warehousing, management reporting and sales force automation. Knowledge of Pharmaceutical Syndicated Data (a plus), such as IMS’ DDD, Xponent/Xponent Plantrak and analytical software, SPSS or SAS, Dendrite SFA (a plus) and Business Objects is required. Must have demonstrated analytical skills, excellent customer service, communication, presentation, and interpersonal skills. Must be proficient in the application of personal computers and software, including extensive experience with report writing applications and the Microsoft Office Suite. Must be able to manage multiple projects effectively using multi- disciplinary resources to meet project and timeline demands and experience interacting with outside vendors. |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Senior Administrative Assistant |
| See above |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior / p-CRF Developer |
| BA/BS in life science, computer science, pharmacy, nursing or equivalent.
Fluent English (oral and written).
1. 2-5 years working experience in software based paper forms design
2. University degree in Life Sciences, Mathematics, Computer Science, Medical Informatics or equiva-lent degree
3. Solid knowledge of medical terminology.
4. Exposure to knowledge of Clinical Research prac-tices and procedures, stages of clinical trials, drug development process, requirements and guidelines for data collection.
5. Solid knowledge of the software used with pCRF design in EDM, specifically the electronic publishing system for pCRF production.
6. Solid communication skills in order to be able to work with a wide variety of customers both face-to-face and via phone or e-mail. Requirement for excel-lent ENGLISH.
7. Exposure to ICH and Health Authority guidelines and regulations as they pertain to clinical database management and computer systems |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| SECURITY OFFICER |
| See above |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Scientist/Senior Scientist, Antibody Drug Conjugates, Drug Discovery - Agensys, Santa Monica, CA |
| PhD in biological sciences, with 5+ years of relevant industrial experiencePrevious background with chemotherapeutic drugs, monoclonal antibodies and/or antibody drug conjugates for oncology with some in vivo tumor biology experience is highly preferred.Excellent analytical, oral and written communication skills and a demonstrated ability to operate both independently and in a team environment.Strong data analytical skills, excellent communication and supervisory skills are required.The qualified candidate should be a highly motivated, strategic thinker with excellent organizational skills who can effectively drive programs forward in a cross functional team oriented environment. |
| Regeneron Pharmaceuticals, Inc. |
Tarrytown |
NY |
9/4/2010
|
| Scientist/Post Doctoral Genome Engineering |
| Technical Skills: Experience with analyzing phenotypes in mutant mice. Experience with genotyping and gene expression analysis techniques. Microscopy techniques. Also experience with ES cells and/or iPS cells. Previous experience as supervisor not required but will also be considered an advantage.
|
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Scientist-Analytical |
| Education
Minimum: BS or equivalent experience.
Desirable: MS or equivalent.
Languages: Fluent English (oral and written)
Experience/Professional requirement:
1. Minimum of 3 successful years of experience as associate scientist (promotional pathway) or 3-5 year's (for BS) or 1-3 year's (for MS).
2. Awareness/proven experience for safe handling of chemicals, potentially dangerous materials and equipment.
3. Good scientific or technical knowledge in a specific area (e.g. synthetic, analytica or galenical).
4. Adequate knowledge in scientific/technical areas of collaboration.
5. Proficient with laboratory and/or technical tools.
6. Adequate knowledge of software and computer tools.
7. Basic presentation skills and scientific/technical writing skills. |
| BD (Becton, Dickinson and Company) |
Research Triangle Park |
NC |
9/3/2010
|
| Scientist- Chemistry |
| See above |
| Regeneron Pharmaceuticals, Inc. |
Tarrytown |
NY |
9/4/2010
|
| Scientist- Assay Development |
| Ph.D. in Biology, Immunology or a related field
-2-5 years of industry or laboratory experience
-Experience developing ELISAs and cell-based assays
-Experience in the validation of ELISAs and cell based assays for protein biopharmaceuticals in a regulated environment under GLPs is required.
-The successful candidate must possess excellent organizational and communication skills
-Must be able to maintain lab notebook and keep a safe lab environment
-The ability to effectively interact with colleagues in a team environment
-Ability to independently plan, supervise and direct projects to completion are essential
|
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Scientist, Translational Safety Biomarker Lab |
| Educational requirements:
BS/MS degree in Biochemistry or Molecular
and/or Cell Biology, Biomedical engineering,
or related fields.
Experience:
5 or more years of practical experience in
assay, reagent, and technology development
in the life sciences industry. The successful
candidate will have experience in molecular
and/or chemical approaches to affinity-
reagent generation. It would be beneficial to
have experience working with biomarker
development, exposure to in vivo studies
both preclinical and/or clinical. The
preferred candidate will have expertise in
data summarization and analysis, oral and
written communication skills. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Scientist, Process Development in Antibody Drug Conjugates - Agensys, Santa Monica, CA |
| ? Ph.D. in a scientific discipline (Chemistry, Chemical Engineering, and Biology) with 5+ years of relevant experience in the pharmaceutical /biotechnology industries.? Knowledge of the design, optimization and scale-up of organic synthesis processes. ? Direct experience in protein purification, conjugation of monoclonal antibodies to small molecules, and process scale-up. ? Experience with HPLC, LC/MS-ESI, chromatographic techniques and immunologic assays including ELISA and immunoblotting? Hands-on experience with unit operations such as lab and pilot-scale bioreactor operation, chromatography, UF/DF, and filtration? Supervisory experience and experience with coordinating activities with CMOs are preferred.? Must be highly motivated, have excellent organizational and communication skills, and must be able to work independently and as part of a multi-disciplinary team. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Scientist, Metabolic Pathways |
| M.S. in Chemistry or Biochemistry or related field with a minimum of three years or B.S. with five years of hands-on with HPLC and LC-MS/MS. Prior experience with radioisotope handling (e.g., 3H, 14C), biochemical techniques and in vivo and in vitro metabolism is required. The candidate should be capable of working independently under moderate supervision and should possess good writing and verbal communication skills. An excellent working knowledge of general laboratory techniques, HPLC and LC-MS/MS operation, and troubleshooting and method development is essential. A strong background in analytical problem solving is also required. |
| GE Healthcare |
Piscataway |
NJ |
9/3/2010
|
| Scientist II-HC |
|
Bachelor?s degree in Biology, Chemistry, Engineering or related Life Science discipline
- 5+ years bioprocess experience in a (bio)chemical laboratory in an industrial setting
- Willingness to travel up to 25-50%
- Prior experience interacting with Customers
- Demonstrated ability to troubleshoot bioprocesses
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
- Master's degree in Biology, Chemistry, Engineering or related Life Science discipline
- Strong industrial experience in purification of biomolecules (upstream, downstream, technology transfer, validation, process development, biomanufacturing)
- Working experience in industrial biopharmaceutical purification
- Experience with chromatography techniques: IEX; HIC; AC; RPC; IMAC and SEC
- Experience with filtration methods- Experience in Disposable biomanufacturing
- Strong Background in the purification of biomolecules
- Experience in working in cGMP environment
- Working knowledge of FDA/EMEA regulations for biologics (Phase I-III manufacture)
- Proven skills working in a global team with global Customers
|
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Scientist II |
| Education & Experience
BS degree required 4 - 8 years of related experience 2+ years demonstrated experience with method development |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Scientist I, DMPK/Exploratory Development |
| * Ph.D. or MS in Analytical Chemistry, Biochemistry, Pharmaceutical Science, or a related discipline
* Ph.D with 0 ? 3 years of experience or MS degree with 3 ? 7 years of experience
* Hands on experience in LC/MS operation, maintenance, and use for sample analysis
* Data processing experience using Analyst software
* Experience with Watson LIMS, and familiarity with GLP guidelines
* Possess superior communication and writing skills
* Be a team player and also have the ability to work independently
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Scientist I - Molecular Toxicology |
| Minimum Requirements
Technical Skill Sets:
? Demonstrated competence in performing a variety of molecular biology techniques (e.g. nucleic acid purification, cloning, TaqMan and SYBR green qPCR, siRNA/shRNA knockdown, etc?)
? Proficiency in isolating and cultivating cells from different organs in different species
? Demonstrated competence in performing a variety of biochemical techniques (e.g., preparation of cell and tissue extracts, subcellular fractionation, enzyme assays, protein detection assays (Western blotting, ELISA, Luminex, MSD?))
? Extensive experience with preclinical animal models, including animal handling, study design and protocol implementation, IV and oral dosing, and necropsy procedures
? Good understanding of SOPs as well as their practical implementation
? Fluency in English
? Working knowledge of relevant IT systems and software
Experience:
? At least 5 years of experience in cellular/molecular biology and/or toxicology in academic and/or industrial environment
? Excellent knowledge of mammalian cell culture models (primary cultures and cell lines) and related techniques
? Excellent knowledge of molecular & biochemical analytical techniques
Personal Skill Sets:
? Interpersonal and teamwork skills
? Independent and proactive work ethic
? Outstanding oral communication and writing skills
? Computer skills for experimental organization, assay design, data collection and analysis, and report writing
Education:
Bachelor?s or Master?s degree in life sciences, preferably molecular biology, biochemistry, cell biology, or molecular toxicology |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Scientist I |
| Bachelor?s Degree in analytical chemistry or a related discipline plus at least 5 years (or M.S. and 3 years) of relevant experience in quantitative analytical techniques involving the automated extraction and analysis of small and/or large molecules in biological samples using LC-MS/MS. Experience in a GLP laboratory environment, proficiency with personal computer applications for word processing, spreadsheets and graphics, as well as good oral and written communication skills are desirable. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Scientist I |
| Minimum 5 years of laboratory experience. Experience with immunofluoresence, fluorescent microscopy and image analysis is required. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Scientist I |
| Education & Experience
BS, MS, or PhD, Chemistry, or other scientifically related field. BS degree + 5 or MS +3 years experience as an analytical chemist or MS, Chemistry with 2+ years experience within method development. |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
9/3/2010
|
| Scientist I |
| See above |
| BD (Becton, Dickinson and Company) |
Research Triangle Park |
NC |
9/3/2010
|
| Scientist - In Vivo |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Scientist |
| See above |
| Eveo |
San Francisco |
CA |
9/4/2010
|
| Scientific Content Director |
| EXPERIENCE/SKILLS REQUIREMENTS
- Advanced life science (PhD, PharmD, MS) or medical (MD, DO) degree;
- 5+ years managing science content development within an agency focused on the pharma/biotech space, preferably digital
- 10+ years’ medical/scientific writing/editing experience
Job Description:
http://docs.google.com/View?id=dqfmzsf_10fzfw9tgv |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Scientific Associate: Oncology Biotherapeutics |
| Candidates should possess a BS/MS degree with 2-5 years of relevant laboratory experience. Candidates who have worked in the Pharma/ Biotech industries are particularly encouraged to apply. Knowledge of cell signaling pathways as related to oncology or other proliferative diseases is crucial. It is essential that you have an excellent working knowledge and direct experience of a breadth of cellular and molecular biological methods (especially RNAi, RT-qPCR, cloning, cell culture, transient/ stable cell line generation, immuno-detection, ELISAs and phenotypic characterization). You should be a scientifically motivated self starter, capable of independently conceiving, conducting and critically analyzing your own innovative experiments. Strong presentation skills, communication and the ability to work in a fast-paced team-oriented environment will also be vital. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Scientific Associate II |
| ? B.S. or M.S. in Analytical Chemistry, Biochemistry or related life science field with a strong background in protein analytics.
? Minimum of 3 years of relevant academic or industrial laboratory experience; hands-on experience with HPLC and CE techniques is required. Experience with mass spectrometry would be a plus.
? Must have excellent written and oral communication skills and demonstrate ability to work both independently and as part of a team.
? Successful candidate should be self-motivated and capable of multi-tasking with strong problem solving skills. |
| BD (Becton, Dickinson and Company) |
Columbus East |
NE |
9/3/2010
|
| SCF Setup (Setup Instruct Repair) 2nd Shift |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| SAP Technical Architect / Solutions Architect |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| SAP Security Analyst |
| See above |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sales Training Business Partner |
| ? Bachelor?s degree
? MBA preferred
Experience:
? 6-8 years professional experience (sales, marketing, operations, management)
? > 2 years of experience in training organization
? Analytic, strategic and creative thinking
? Innovative mindset
? Knowledge of sales training and development processes
? Strategic and business acumen
? Strong prioritization, negotiation and influencing skills
? Knowledge of adult learning principles & concepts
? Strong oral, written and platform skills
? 3 to 5 years of Pharmaceutical industry experience preferred
? Understanding of Novartis BU structure and markets |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Sales Trainer |
| - Bachelor's degree
- Minimum of 3 years experience in pharmaceutical sales or healthcare
- Experience in training, curriculum design, and delivery
- Thorough knowledge across therapeutic areas
- Demonstrated leadership, communication and organizational skills
- Thorough understanding of market dynamics within the therapeutic areas
- Demonstrated consistent success as a Pharmaceutical Sales Specialist
- Hospital or CVAS experience preferred |
| Daiichi Sankyo, Inc. |
Wilkes Barre |
PA |
9/3/2010
|
| Sales Representative, Primary Care 3 - Wilkes Barre, PA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Terre Haute |
NJ |
9/3/2010
|
| Sales Representative, Primary Care 3 - Terre Haute, IN |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Sales Representative, Primary Care 3 - Santa Monica, CA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
San Diego |
CA |
9/3/2010
|
| Sales Representative, Primary Care 3 - San Diego, CA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Saint Paul |
MN |
9/3/2010
|
| Sales Representative, Primary Care 3 - Saint Paul, MN |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Rocky Mount |
NC |
9/3/2010
|
| Sales Representative, Primary Care 3 - Rocky Mount, NC |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Reading |
PA |
9/3/2010
|
| Sales Representative, Primary Care 3 - Reading, PA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Pikeville |
KY |
9/3/2010
|
| Sales Representative, Primary Care 3 - Pikeville, KY |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Oklahoma City |
OK |
9/3/2010
|
| Sales Representative, Primary Care 3 - Oklahoma City North, OK |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Oceanside |
NJ |
9/3/2010
|
| Sales Representative, Primary Care 3 - Oceanside, CA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Washington |
DC |
9/3/2010
|
| Sales Representative, Primary Care 3 - North Washington, DC |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Newport News |
VA |
9/3/2010
|
| Sales Representative, Primary Care 3 - Newport News, VA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
New Haven |
CT |
9/3/2010
|
| Sales Representative, Primary Care 3 - New Haven, CT |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Monterey |
CA |
9/3/2010
|
| Sales Representative, Primary Care 3 - Monterey, CA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Massapequa |
NY |
9/3/2010
|
| Sales Representative, Primary Care 3 - Massapequa, NY |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Madison |
WI |
9/3/2010
|
| Sales Representative, Primary Care 3 - Madison, WI |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Las Vegas |
NV |
9/3/2010
|
| Sales Representative, Primary Care 3 - Las Vegas, NV |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Las Cruces |
NM |
9/3/2010
|
| Sales Representative, Primary Care 3 - Las Cruces, NM |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Lansdale |
PA |
9/3/2010
|
| Sales Representative, Primary Care 3 - Lansdale, PA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Lafayette |
IN |
9/3/2010
|
| Sales Representative, Primary Care 3 - Lafayette, IN |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Kingsport |
TN |
9/3/2010
|
| Sales Representative, Primary Care 3 - Kingsport, TN |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Jackson |
MS |
9/3/2010
|
| Sales Representative, Primary Care 3 - Jackson South, MS |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Houston |
TX |
9/3/2010
|
| Sales Representative, Primary Care 3 - Houston West, TX |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Fredericksburg |
VA |
9/3/2010
|
| Sales Representative, Primary Care 3 - Fredericksburg, VA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Fort Lauderdale |
FL |
9/3/2010
|
| Sales Representative, Primary Care 3 - Fort Lauderdale, FL |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Fond du Lac |
WI |
9/3/2010
|
| Sales Representative, Primary Care 3 - Fond du Lac, WI |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Chesapeake |
VA |
9/3/2010
|
| Sales Representative, Primary Care 3 - Chesapeake, VA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Charleston |
SC |
9/3/2010
|
| Sales Representative, Primary Care 3 - Charleston, SC |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Baltimore |
MD |
9/3/2010
|
| Sales Representative, Primary Care 3 - Baltimore West, MD |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Allentown |
PA |
9/3/2010
|
| Sales Representative, Primary Care 3 - Allentown, PA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Walnut Creek |
CA |
9/3/2010
|
| Sales Representative, Primary Care 2 - Walnut Creek, CA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Tucson |
AZ |
9/3/2010
|
| Sales Representative, Primary Care 2 - Tucson, AZ |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Terre Haute |
IN |
9/3/2010
|
| Sales Representative, Primary Care 2 - Terre Haute, IN |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Syracuse |
NY |
9/3/2010
|
| Sales Representative, Primary Care 2 - Syracuse, NY |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Salina |
KS |
9/3/2010
|
| Sales Representative, Primary Care 2 - Salina, KS |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Sacramento |
CA |
9/3/2010
|
| Sales Representative, Primary Care 2 - Sacramento West, CA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Oklahoma City |
OK |
9/3/2010
|
| Sales Representative, Primary Care 2 - Oklahoma City North, OK |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
New Rochelle |
NY |
9/3/2010
|
| Sales Representative, Primary Care 2 - New Rochelle, NY |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Manhattan |
NY |
9/3/2010
|
| Sales Representative, Primary Care 2 - Manhattan S, NY |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Lufkin |
TX |
9/3/2010
|
| Sales Representative, Primary Care 2 - Lufkin, TX |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Lafayette |
IN |
9/3/2010
|
| Sales Representative, Primary Care 2 - Lafayette, IN |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Jacksonville |
FL |
9/3/2010
|
| Sales Representative, Primary Care 2 - Jacksonville West, FL |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Jacksonville |
FL |
9/3/2010
|
| Sales Representative, Primary Care 2 - Jacksonville South, FL |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Houston |
TX |
9/3/2010
|
| Sales Representative, Primary Care 2 - Houston Central, TX |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Gulfport |
MS |
9/3/2010
|
| Sales Representative, Primary Care 2 - Gulfport, MS |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Des Moines |
IA |
9/3/2010
|
| Sales Representative, Primary Care 2 - Des Moines W, IA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Dallas |
TX |
9/3/2010
|
| Sales Representative, Primary Care 2 - Dallas East, TX |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Brooklyn |
NY |
9/3/2010
|
| Sales Representative, Primary Care 2 - Brooklyn North, NY |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Billings |
MT |
9/3/2010
|
| Sales Representative, Primary Care 2 - Billings, MT |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Asheboro |
NC |
9/3/2010
|
| Sales Representative, Primary Care 2 - Asheboro, NC |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Wichita Falls |
TX |
9/3/2010
|
| Sales Representative, Primary Care 1 - Wichita Falls, TX |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Topeka |
KS |
9/3/2010
|
| Sales Representative, Primary Care 1 - Topeka, KS |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
San Jose |
CA |
9/3/2010
|
| Sales Representative, Primary Care 1 - San Jose, CA |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Salina |
KS |
9/3/2010
|
| Sales Representative, Primary Care 1 - Salina, KS |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Pittsburgh |
PA |
9/3/2010
|
| Sales Representative, Primary Care 1 - Pittsburgh West, PA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Orange |
CA |
9/3/2010
|
| Sales Representative, Primary Care 1 - Orange, CA |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Oceanside |
CA |
9/3/2010
|
| Sales Representative, Primary Care 1 - Oceanside, CA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Louisville |
KY |
9/3/2010
|
| Sales Representative, Primary Care 1 - Louisville South, KY |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Las Cruces |
NM |
9/3/2010
|
| Sales Representative, Primary Care 1 - Las Cruces, NM |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Hagerstown |
MD |
9/3/2010
|
| Sales Representative, Primary Care 1 - Hagerstown, MD |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Gulfport |
MS |
9/3/2010
|
| Sales Representative, Primary Care 1 - Gulfport, MS |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Evanston |
IL |
9/3/2010
|
| Sales Representative, Primary Care 1 - Evanston, IL |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Columbus |
OH |
9/3/2010
|
| Sales Representative, Primary Care 1 - Columbus South, OH |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Cleveland |
OH |
9/3/2010
|
| Sales Representative, Primary Care 1 - Cleveland West, OH |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Chico |
CA |
9/3/2010
|
| Sales Representative, Primary Care 1 - Chico, CA |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Chesapeake |
VA |
9/3/2010
|
| Sales Representative, Primary Care 1 - Chesapeake, VA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Binghamton |
AL |
9/3/2010
|
| Sales Representative, Primary Care 1 - Binghamton/Elmira, NY |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Atlanta |
GA |
9/3/2010
|
| Sales Representative, Primary Care 1 - Atlanta West, GA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| GE Healthcare |
na |
CA |
9/3/2010
|
| Sales Representative 1-HC |
|
* Bachelor of Science Degree in a Life Science/Sciences
* 2 or more years sales experience within a Life Sciences or Medical Device industry
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
* Experience with distributor sales
* Experience working in and managing client in a laboratory environment
|
| Astellas Pharma, Inc. |
Phoenix |
AZ |
9/3/2010
|
| Sales Director PCP & Specialty- West Coast |
| REQUIREMENTS:- 8+ years pharmaceutical sales and sales 6 years pharmaceutical sales management experience, some of which needs to be at the director level. - Extensive knowledge of sales processes and pharmaceutical products and industry- Excellent communication, facilitation and presentation skills- Can do approach and excellent motivational and persuasion skills- Leadership skills commensurate with the position- BA/BS degree is required - Extensive travel is required for this position |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Sales Contract Administrator |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Sales Contract Administrator |
| See above |
| Novartis Oncology |
na |
AR |
9/4/2010
|
| Sales Analyst-Walmart |
| ? Bachelor?s Degree
? Demonstrate advanced knowledge of Excel, Word, powerpoint, and Access
? Flexible with traditional work hours: willing to work several hours on Sunday evening from home or early AM hours on Monday to meet deadlines
? Exceptional Communication and Interpersonal skills
? Able to work in a fast-paced environment with demonstrated ability to juggle multiple competing tasks and demands.
? Preferred experience within Consumer Products Goods Company |
| Agilent Technologies, Inc. US |
Chandler |
AZ |
9/4/2010
|
| Sales - Genomics Product Specialist |
| - Minimum BS/MS in Chemistry or a Life Sciences discipline, or equivalent.
- Solid self management and organizational and prioritization skills
- 5+ years related direct sales experience with a demonstrated track record of successfully selling against a quota.
- High level of experience in microarrays and/or NGS.
- Technical knowledge and domain knowledge in the research and diagnostic sector of the pharmaceutical industry (profit and not for profit. Knowledge of the cytogenetics market.
- Industry/Application expertise. Working knowledge of competitive products (specifications, value propositions, price points).
- Comfortable interfacing with senior managers within your customers.
- Demonstrated commercial selling skills. Strong business development and sales closing skills.
- Effective interpersonal communication and telephone sales skills.
- Must be able to travel up to 35% of the time.
Geo Location: Arizona (preferred) or Texas |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Safety Toxicologist |
| ? BS or MSc degree and major in physiology, pharmacology, biomedical engineering or related field.
? Prefer 5 ? 10 years experience in cardiovascular physiology and/or pharmacology research.
? Prefer minimum of 2 years experiences in cardiovascular safety pharmacology research.
? Experience in setting up, conducting and reporting of telemetry studies in dog and monkey.
? Familiar with EMKA jacket system or other external jacket telemetry system and have experience in EMKA ECGAuto computer software (or similar computer software) to analyze cardiovascular telemetry data.
? Experience in using Excel and SAS macro to analyze and report cardiovascular parameters in telemetry.
? Experience in ECG analyses including ECG interval measurements and waveform abnormalities screening in dog and monkey. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Safety Scientist/Principal Safety Scientist, Oncology |
| Minimum of Bachelor?s Degree in Science or Pharmacy or Nursing required.Minimum of 5 years pharmaceutical experience in a clinical safety/research department required.Minimum of 5 years of medical writing experience (Prefer experience in writing pharmaceutical reports such as Clinical Study Reports, Safety sections of the ISS and/or EU Common Technical document, PSUR or white paper).Proven ability to critically evaluate medical data.Proven understanding of clinical disease state and implications of treatment.Proven ability to communicate effectively (verbal, presentation at group meetings, etc).Proven experience with project management (formal or informal).Prefer experience in training or mentoring.Strategic thinking, Organizational, Leadership, Results-oriented performance, Team player.Excellent knowledge of ICH, US & EU regulations and requirements for pharmacovigilance (experience with world-wide safety reporting regulations and guidelines required).Excellent interpersonal skills, including ability to work effectively cross culturally and cross functionally.Proven ability to effectively lead cross-functional teams with respect to risk management activities and to influence where direct reporting line relationships do not exist. Excellent written and spoken English |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Safety Medical Director |
| M.D. required; 3+ years of
pharmaceutical pharmacovigilance experience, ideally both pre- and
post-marketing.
- Solid knowledge of general medicine and clinical practice, evidenced by
medical training and/or medical practice experience.
- Strong leadership skills, as well as experience working in a matrix
environment.
- Must have a strong working knowledge of FDA regulations/ICH guidelines
- Must be experienced in safety reviews of IBs, protocols, final clinical study
reports, and summaries of safety.
- Advanced ability to read, analyze and interpret clinical data and information
- Possess very strong writing skills and advanced verbal communication and
presentation skills.
- Requires strong attention to detail in writing and/or proofing materials
- Ability to work in a fast paced environment with demonstrated ability to
simultaneously manage multiple competing tasks and demands.
- Ability to work independently, take initiative and complete tasks to
deadlines.
- Occasional domestic and international travel may be required (
Vertex Pharmaceuticals |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
9/3/2010
|
| Safety Intern |
| See above |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Safety Database Applications Specialist, Global Patient Safety |
| * A bachelor?s degree in a technical discipline or a technical degree.
* A minimum of 1 year hands-on analysis and application support experience in a Windows O/S application environment supporting multi-tiered application architecture to include web based application clients.
* Approximately 1 year experience in drug safety and/or data management with knowledge and experience with ARISg, or a comparable commercial safety database/system, including configuration/operational support.
* Familiarity with GCP, FDA, EMEA regulatory requirements as they apply to pharmacovigilance and drug safety and working knowledge of database design and system life-cycle concepts.
* Familiarity with Signal Detection tools (Empirica, Multi-item gamma Poisson (MGPS), etc)
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| RF Field Applications Engineer |
| Position requires Bachelors or Master Degree or equivalent and a minimum of 2-4yrs+ in an Applications Engineering or Sales Support role.
? Must be US citizen.
? Must have knowledge of RF and microwave products such as network analyzers, signal generators and spectrum analyzers.
? Candidate must be knowledgeable of competition and able to identify lockout specification (identify Agilent's competitive advantage over competition)
? Must be able to analyze customer requirements and recommend appropriate solutions
? Must possess excellent communication skills |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Respiratory Specialist - Toms River, NJ PEXC1E |
| ? Bachelor?s Degree (preferably in Life Sciences, Pharmacy or Business related discipline).
? Minimum of 4+ years of Specialty sales experience selling in the Respiratory/Allergy and/or Infusion market and interacting with Allergists, Pulmonologists, and other key customers.
? Track record of success in account based selling models within Specialty Markets
? Knowledge and understanding of distribution and reimbursement models used for Specialty/Biologic products.
? Demonstrated superior business acumen and business planning skills.
? Proven ability to collaborate and work cross functionally with internal and external partners.
? Possess high achievement drive, self-motivation, and willingness to mentor others
? Effective problem solving, decision making and interpersonal skills (both internal and external).
? Exceptional customer relationship building skills.
? Strong Analytic and Computer literacy skills. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Research Scientist: Biochemistry and Affinity Proteomics (BS/MS) |
| Candidates should have a BS or MS in Biochemistry or Biological Science with 3-8 years academic and/or industry experience. They must be well-versed in all aspects of protein purification including sample preparation, chromatographic and gel-based separations, electrophoresis, and cell culture. They should have experience in the design and implementation of biochemical assays and in data analysis. The ideal candidate is an independent worker, a self-starter, good at trouble shooting and thriving in a multidisciplinary environment. Excellent communication skills are required and a premium is placed on candidates with a track record of creativity and innovation.
Additional Experience:
Experience with activity-based probes, photoaffinity crosslinkers, sub-cellular fractionation, basic molecular biology techniques, and sample preparation for mass spectrometry is a plus. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Research Scientist, Pharmacology - Agensys - Santa Monica, CA |
| Candidate consideration requires a Ph.D., or an equivalent degree, in Biology, Pharmacology, Immunology, Biochemistry or a related field with a minimum of 3 years of post-doctoral experience. Previous hand-on experience using human tumor xenograft models in oncology research, as evidenced by publications, is required. Understanding the basic concepts of pharmacokinetics and pharmacodynamics and be able to analyze relevant data are highly desired. Experience in human tumor xenograft and primary cell line development is a definite plus. Previous experience in preclinical evaluation of cancer therapeutics using xenograft models preferably in an industry drug discovery setting and experience managing research associates are preferred. Successful candidates should have strong written and oral communication skills, be self-motivated and able to demonstrate leadership. Developmental opportunities include leading research projects and building new technology platforms. |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Research Scientist II |
| The ideal candidate for this position will be highly motivated and minimally have an MS degree with at least 10 years, or a PhD or DVM with at least 8 years of hands-on experience in using relevant general/safety pharmacology assays, such as cardiovascular telemetry or Langendorff heart perfusion.
Extensive understanding of cardiovascular pharmacology and physiology is required. Demonstrated independent thinking, trouble-shooting skills, and ability to analyze, interpret, and translate physiological function data is a must. Industry non-clinical research experience and experience with assessing drug-induced QT prolongation is preferred. Extensive knowledge of Data Sciences International/Ponemah (P3P and DataQuest), EMKA Technologies, or similar software packages is necessary. Ability to write basic programs using SAS software for data analysis and statistics is a plus.
The candidate must be able to work independently and in a matrix and function team environment. Strong written and oral communication skills are required, including excellent report writing and presentation skills. Study outsourcing and/or supervisory experiences are a plus.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Research Scientist ? RNAi Therapeutics (BS/MS) |
| This position requires a Bachelor?s or Master?s degree in Biology, Cell/Molecular Biology, Biochemistry, Genetics, or related field with 5-10 years of academic or industrial research experience. Proven track record of innovative project contributions including peer-reviewed publications is desired. The successful candidate will have extensive experience with basic molecular and cellular biology techniques such as mammalian cell culture, siRNA technologies, real-time PCR, molecular cloning, and compound efficacy profiling. Experience in high-throughput screening technologies and in-vivo animal models are a plus. Good organizational and analytical skills, a working knowledge of data management, word processing, and graphing software are essential. Additionally, the ideal candidate will have excellent oral/written communications skills with the ability to work both independently and in the context of a multidisciplinary team of chemists, biologists, and pharmacologists. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Research Scientist |
| Education requirements:
BS or MS in chemistry or related scientific discipline with 2+ years experience in a laboratory setting
or
Entry-level PhD in Chemistry or related scientific discipline.
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Research Quality Assurance Associate - Agensys, Santa Monica, CA |
| ? PhD in Life Sciences preferred.? Minimum 2 years in a pharmaceutical development environment with solid knowledge and review experience of in-vivo and in-vitro study protocols and reports. Additional quality assurance experience in a research environment with programs such as document management and equipment qualification is recommended.? In-depth understanding of pre-clinical pharmacology studies. ? Strong oral and written communication skills are required.? Strong interpersonal skills and the ability to work in a project team environment are a requirement. ? Fluency with Word, Excel, and Access databases is recommended. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Research Investigator, Preclinical Imaging, Investigative Toxicology |
| ? Ph.D. degree in Biochemistry, Physiology, Pharmacology, Toxicology, Biophysics, Biomedical Engineering or related field in the biomedical sciences
? At least 2 years of prior experience in pharmaceutical drug development and/or toxicological sciences required.
? Experience with hands-on in vivo small animal imaging, preferably with multiple imaging modalities. A strong expertise in small animal (rat, mouse) Ultrasound imaging for various applications including contrast enhanced ultrasonography is preferred.
? Expertise and knowledge in vascular toxcology and in vitro vascular ring assay would be a plus.
? Experience of managing highly skilled technical staff, laboratory equipment, consumables and safety is desirable.
? Fluency in English (written and spoken) is a must
? Flexibility and ability to work in a team, comfortable with multitasking, excellent interpersonal skills to communicate and collaborate within a multi-disciplinary environment, willingness to take on additional responsibilities are expected
? Excellent project management skills
Technical Skill Requirements:
? Experience with pre-clinical applications of MR imaging and spectroscopy, X-ray microCT, ultrasound and/or optical imaging
? Imaging data processing and analysis |
| Novartis Oncology |
na |
CO |
9/4/2010
|
| Research Chemist III |
| Educational/Professional Requirements:
?BS/BA in Chemistry or life sciences
?4 years of professional related experience
?Relevant experience in a GMP laboratory and R&D lab/ production environment.
?Infrequently lifting 5kg to waist height,
?Approx 10% on floor time (Walking/Standing)
?Limited Travel (1-5 times/yr.)
Skills & Competencies:
?Has thorough understanding of technical concepts required for raw material testing, method development, evaluation and optimization.
?Requires working knowledge of Microsoft office applications. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Research Associate/Senior Research Associate: Target function ? MAb assays - Agensys, Santa Monica, CA |
| The position requires a BS or MS in Biology or a related field with a minimum 3 years of practical experience in a research laboratory in the required activities. Industry experience and previous work in biochemical, immunological, cell culture and cell-based techniques are essential. Excellent verbal and communication skills, and the ability to work both independently and in a team environment are required. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Research Associate/Senior Research Associate: Antibody Drug Discovery - Agensys, Santa Monica, CA |
| The position requires a BS or MS in Biology or a related field with a minimum 3 years of practical experience in a research laboratory in the required activities. Previous work in biochemical, immunological, cell culture and cell-based techniques are essential. Industrial experience is preferred. Excellent verbal and communication skills and the ability to work both independently and in a team environment are required. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Research Associate/ Senior Research Associate ? Molecular Biology - Agensys, Santa Monica, CA |
| The ideal candidate will have M.S. (preferred) or B.S. in Molecular Biology or related field, with a minimum of five (5) years of relevant research experience. Experience in molecular biology techniques and methods, with emphasis on gene expression and gene structure analysis is required. The ability to reliably handle and process precious and limited specimens is essential. Excellent verbal and written communication skills, as well as the ability to work both independently and in a team environment are required. |
| Regeneron Pharmaceuticals, Inc. |
Tarrytown |
NY |
9/4/2010
|
| Research Associate- Therapeutic Antibodies |
| The ideal candidate should have BS degree in immunology, Biology, Biochemistry, or related discipline. Candidates with work experience in the area of immunization and monoclonal antibody development are most desirable. Minimum of 3-5 years laboratory experience is required. Knowledge of B cell development is a significant plus. Must be able to work productively in a fast-paced collaborative team environment. Excellent communication skills are essential.
|
| Regeneron Pharmaceuticals, Inc. |
|
|
9/4/2010
|
| Research Associate- Protein Sciences |
| Requirements:
- B.S or MS or equivalent in biochemistry
- 0-3 years post-graduate experiences in protein biochemistry
- Knowledge in LC/MS for protein and peptide analysis
- Strong organization and communication skills and effective interpersonal skills
- Ability to learn new technologies and solve problems
- Ability to work in a team environment
|
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Research Associate, Protein Science - Agensys, Santa Monica, CA |
| Candidate consideration requires a B.S. or M.S. in chemistry, biochemistry or similar field with a minimum of 2 years of laboratory experience. Industrial experience protein analysis and protein purification is highly preferred. Experience in proteomic method development and hands on experience with Biacore are also preferred. The successful candidate will have strong written and oral communication skills, be self-motivated, possess strong organizational skills, and have a track record of working successfully in a team environment. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Research Associate, Molecular Imaging, PET/SPECT/CT |
| The ideal candidate will have a BS/MS in Biology, Biochemistry, Animal Sciences, Bioengineering, Biophysics or related field, and 3+ years of hands-on experience with PET/SPECT/CT imaging is a requirement, ideally in a drug discovery environment. Good organizational, interpersonal skills, and excellent communication and presentation skills are desirable.
Skills required: Technical proficiency in all aspects related to PET and extensive hands-on experience with small animal handling (including tail vein injection, catheter placement, perfusion, microdissection), and in vivo pharmacology. Strong computer/computational skills in data analysis. Creativity and the ability to work independently. |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
9/3/2010
|
| Research Associate III |
| See above |
| Regeneron Pharmaceuticals, Inc. |
Tarrytown |
NY |
9/4/2010
|
| Research Associate II - Bispecifics |
| The qualified individual will possess a Bachelor's degree in Biology or related medical science with 1-3 years laboratory experience or a Master's degree and 0-1 years experience. Must be able to work productively in a fast-paced collaborative team environment. The candidate should have experience in protein expression vector construction and analysis as well as in conducting cell based assays. Experience with ELISA assays is also a plus. Excellent communication skills are essential. Candidate should be proficient in Microsoft Office and statistical analysis programs. A background in immunology or oncology is highly desirable. |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
9/3/2010
|
| Research Associate II |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
9/3/2010
|
| Research Associate II |
| See above |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Research Associate BS/MS - Biochemistry/Enzymology |
| The successful candidate should have a Bachelors/Masters in biochemistry or a related area of biological sciences with at least 2 years of laboratory experience in industry or academic setting. Experience in biochemical and biophysical assay development, enzyme kinetics is desirable. Knowledge and hands-on experience in applying modern biophysical/analytical techniques, such as fluorescence spectroscopy, Surface Plasmon Resonance, Calorimetry and LC-MS, are a plus. Must be self-motivated and detail-oriented. Is highly organized and has ability to handle multiple tasks. Proficiency in data handling with standard computer programs is a must. The candidate should have strong communication and interpersonal skills. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Research Associate /Senior Research Associate in vivo validation, Agensys - Santa Monica, CA |
| The ideal candidate should have a bachelor or master degree in biological sciences with a minimum of 2 years of related research experience after graduation, preferably in an industry setting. Previous experiences in handling research rodents, especially immunodeficient mice in oncology research and human cancer cell culture are absolutely required. Experiences in pre-clinical validation of cancer therapeutics using human tumor xenograft models, microsurgical procedures in laboratory rodents, human tumor xenograft characterization and human cancer primary cell line establishment are highly desired. We are seeking a flexible, enthusiastic individual with good organizational and communication skills and the desire to work in a dynamic team environment. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Research Associate - Cell Biology and Molecular Virology |
| Qualified candidates will have a BS/BA or Master?s degree in biology or related field, with strong data management skills and extensive molecular/cell biology expertise. The candidate should have experience in experimental design, data interpretation and statistical analysis. A strong work ethic, excellent oral and written communication skills, and ability to function in an interdisciplinary team setting are required. |
| Astellas Pharma, Inc. |
Skokie |
IL |
9/3/2010
|
| Research & Development Future Opportunities |
| ? Positions in the Research & Development division at Astellas require degrees in science; advanced degrees plus industry experience are preferred. |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Repair Technician II |
| See above |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Reliability Engineer |
| You will need to have a university degree level or equivalent (complemented by a post-graduate degree and/or certification/license). You'll also bring at least 8 years' relevant experience. An accomplished leader and influencer, Agilent is where your expertise and solutions oriented approach will take you even further.
Required Qualifications:
1. BS in Engineering / Science or equivalent with a minimum of 8 years of relevant functional experience in Reliability and Quality.
2. Post Graduate and / or certification may be required.
3. Demonstrated strong communication skills particularly around the ability to translate reliability terms and concepts such as MTBF, AFR, and ALT into objectives that engineering teams can relate to and understand.
4. Demonstrated skill in teamwork within an organization and across sites as a proactive partner.
5. Demonstrated ability to provide leadership through credibility with R&D teams based on knowledge of reliability planning, relevant testing and customer advocacy.
6. Demonstrated results orientation/accountability. Ability to remain objective given conflicting or missing information and ability to identify what should be done to fill the Gap.
7. Demonstrated skill in planning and organization particularly as it applies to judgment of priorities while managing multiple projects and tasks.
This position is located in Santa Clara, CA |
| Regeneron Pharmaceuticals, Inc. |
|
|
9/4/2010
|
| Regulatory Associate IV |
| Requires a MD or PhD and a minimum of 5 years of pharmaceutical industry experience. Research laboratory, process development or manufacturing experience with biotechnology products is highly desirable.
*Advanced knowledge of 21 CFR Parts 50, 54, 56, 58, 210, 211, 312, 314, 600, 601, and monitors newly published FDA guidelines and international guidance documents in the context of new and ongoing development programs. Negotiation and communication skills a must.
|
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Regulatory Associate |
| Minimum Education Required:
HS or equivalent. BS in scientific discipline preferred.
Minimum Experience Required:
3 years employment in the areas of product registration, compliance or quality systems.
Experience gained through employment in a medical device or drug company preferred.
Minimum Skills Required:
Familiar with global registration and compliance requirements.
Competent in basic documentation requirements.
Basic word processing skills.
Good communications skills (verbal and written).
Computer literacy with CIBA VISION standard software platforms.
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules. |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Regulatory Affairs Specialist |
| See above |
| Novartis Oncology |
na |
SC |
9/4/2010
|
| Regl Scientific Mgr/Dir--Primary Care (North Carolina/South Carolina) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Therapeutic Areas and/or in a Field-based position is a definite asset. Salary flexible.
Ability to travel approximately 60%. |
| Novartis Oncology |
na |
CA |
9/4/2010
|
| Regl Scientific Mgr/Dir Southwest OU--Respiratory (Northern CA) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Respiratory Therapeutic Areas and/or in a Field-based position is a definite asset. Salary flexible. |
| Novartis Oncology |
na |
MO |
9/4/2010
|
| Regl Scientific Mgr/Dir Southwest OU--Respiratory (AR, KS, and MO) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Respiratory Therapeutic Area and/or in a Field-based position is a definite asset. Salary flexible. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Regl Scientific Mgr/Dir Southeast OU--IDTI (AL, FL, GA) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Infectious Diseases, Transplantation and Immunology Therapeutic Areas and/or in a Field-based position is a definite asset. Salary flexible. |
| Novartis Oncology |
na |
NE |
9/4/2010
|
| Regl Scientific Mgr/Dir NW OU--Primary Care (IA and NE) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Cardiovascular, Endocrinology, and Rheumatology Therapeutic Areas and/or in a Field-based position is a definite asset. Salary flexible. |
| Novartis Oncology |
na |
WA |
9/4/2010
|
| Regl Scientific Mgr/Dir NW OU--Primary Care (AK and WA) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Cardiovascular, Endocrinology, and Rheumatology Therapeutic Areas and/or in a Field-based position is a definite asset. Salary flexible. |
| Novartis Oncology |
na |
UT |
9/4/2010
|
| Regl Scientific Mgr/Dir NW OU--Multiple Sclerosis (CO, IA, NE, UT) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Multiple Sclerosis or Related Therapeutic Areas and/or in a Field-based position is a definite asset. Salary flexible. |
| Novartis Oncology |
na |
PA |
9/4/2010
|
| Regl Scientific Mgr/Dir NE OU--Multiple Sclerosis (Phila/Southcent PA) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Mutiple Sclerosis or Related Therapeutic Areas and/or in a Field-based position is a definite asset. Salary flexible. |
| Novartis Oncology |
na |
NY |
9/4/2010
|
| Regl Scientific Mgr/Dir NE OU--Multiple Sclerosis (New York City) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Multiple Sclerosis or related Therapeutic Areas and/or in a Field-based position is a definite asset. Salary flexible. |
| Novartis Oncology |
na |
AZ |
9/4/2010
|
| Regl Scientific Mgr/AD, Hematology MSL, Southwest US |
| Position will be filled at level commensurate with experience. Advanced scientific degree (MD, PhD, or PharmD highly preferred) or oncology nurse with advanced degree required. Minimum of 5 years Oncology experience with a strong current working knowledge of Oncology required. Teaching experience preferred. Previous pharmaceutical industry experience preferred. Thought leader development experience is a plus. Knowledge of treatment guidelines, clinical research processes, FDA regulations and OIG guidelines is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important external customers, including medical thought leaders, academic institutions, large group practices, medical directors and pharmacy directors is required. Must be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society (ies) is a plus. Must be a strong team player who can effectively interface cross-functionally with Novartis clinical and commercial personnel. Working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel) and associated hardware is required. The position is associated with approximately 65% travel. |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Regional Sr. Financial Analyst - Americas (Inventory & Supply Chain) |
| * B.S. Degree in Accounting, Finance, Supply Chain, Operations Management
* 5+ years financial experience, manufacturing experience
* Excellent PC skills and experience including SAP, Excel and Powerpoint
* Ability to travel approximately 10% of the time
* Excellent analytical, judgment and process improvement capabilities
* Demonstrated ability to influence senior leaders, cross functionally and across geographic boundaries to achieve results
* Exceptional communication and interpersonal skills, including oral and written
* Demonstrated ability to perform in an environment that emphasizes teamwork
* Demonstrated capacity to effectively manage multiple and frequently changing priorities
* High degree of accuracy with attention to detail
* Demonstrated ability to meet strict deadlines
Preferred Background:
* MBA
* Fluency in Spanish or Portuguese
* Pharmaceutical industry experience |
| Astellas Pharma, Inc. |
Jersey City (1V010400) |
NJ |
9/3/2010
|
| Regional Sales Manager - Specialty; Jersey City, NJ |
| Job Requirements:- Valid driver's license - Minimum of 5-7 years experience in pharmaceutical sales or related fields, including primary care and specialty sales (preferably hospital sales experience) . - Prior experience in managing field representatives is preferred - Must provide evidence of leadership skills and successful contributions outside immediate team (i.e., training, mentoring, process development, etc.) - A demonstrated high degree of proficiency in managing multiple projects - Proven presentation, coaching, and teaching skills. - Demonstrated ability to consistently meet and exceed sales quota goals - Proficient with basic computer skills. - 4 year college degree |
| GE Healthcare |
na |
CA |
9/3/2010
|
| Regional Sales Director - West Region |
|
* A minimum of 5 successful years selling ion the life sciences market
* Demonstrated success in sales strategy development and implementation
* A bachelors degree
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
* Excellent communication, presentation, and interpersonal relation skills
* Demonstrated negotiation skills
* Strong sales data analysis skills
* Proven ability to manage a budget
* Goal focused leader capable of building a strong teamwork environment
|
| Novartis Oncology |
na |
MS |
9/4/2010
|
| Regional Sales Director - Jackson, MS or Birmingham, AL. |
| Minimum Education Required:
BS/BA in related field. MBA preferred.
Minimum Experience Required:
10+ years experience in outside sales in business to business selling models using consultative selling approaches including a minimum of three (3) years of Sales Management experience.
Demonstrated experience developing and promoting Sales employees.
Proven market analytical sales resulting in performances that exceed company expectations.
Preferred Experience Level:
10+ years business-to-business selling in combination with medical sales experience.
5+ years Front Lines Sales Management experience with a history of exceeding District/Region Sales and Market Share.
People management accountability required. |
| AstraZeneca Pharmaceuticals |
Houston |
TX |
9/4/2010
|
| Regional Sales Director - CV - Cleveland OH |
| Qualifications:
*Bachelor's degree.
*Minimum of 10 years experience in pharmaceutical sales or healthcare, must have management experience in field sales.
*Ability to identify strategies with greatest business impact, formulate an appropriate business plan and enroll their teams to execute the plan.
*Demonstrated leadership and communication competencies, and experience in managing budgets are required.
*Thorough understanding of customer segments and regional market dynamics within all therapeutic areas.
*Ability to lead and manage district sales leaders and to develop staff through coaching and mentoring.
*Exhibited ability to manage multiple, concurrent work-streams in diverse functional/therapeutic areas.
*Previous successful work experience in team selling environments, inclusive of successful management of teams.
*Demonstrated presentation and negotiation skills.
*MBA and/or prior experience in multiple commercial functions (e.g. Marketing, Managed Markets). |
| Novartis Oncology |
na |
PR |
9/4/2010
|
| Regional Medical Associate Director/Director (Puerto Rico) |
| The candidate must be locally based in Puerto Rico.
Position will be filled at level commensurate with experience:
Advanced scientific degree (M.D., Ph.D., or PharmD; M.D. is preferred). A minimum of 3 years of Postdoctoral experience in pharmaceutical industry (preferred) or other healthcare/managed markets environment.
Excellent interpersonal and oral and written communication skills in both English and Spanish are required.
Field based medical and/or managed care with teaching experience preferred.
Thorough knowledge of clinical medicine, managed markets, pharmacoeconomics, disease management, medical research and health policy in Puerto Rico are required.
Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations and ethical guidelines applied to the pharmaceutical industry preferred. Excellent presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, pharmacy directors and government officials is required. Must be science-oriented and be able to prioritize work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer?s unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, Powerpoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Operating Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RMAD/D position is associated with approximately 60% travel. Salary flexible. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Regenerative Medicine Research Associate (BS/MS) |
| Candidates should have a BS or MS in an appropriate discipline as well as 3 or more years relevant experience. The successful candidate should have demonstrated experience with stem cell isolation, culture and characterization, complex cell-based assays and imaging-based screens. Experience in studying the development or regeneration of specific organs such as pancreas, kidney, eye, lung, intestine or skin would be of high interest.
Excellent communication skills and ability to work in a team is required. |
| Agilent Technologies, Inc. US |
Everett |
WA |
9/4/2010
|
| R&D Signal Processing Software Engineer |
| Key Required Skills:
? Bachelors or Masters Degree or University Degree in Electrical Engineering or Computer Science
? Must have 5+ years applicable experience in software development involving signal processing theory, techniques and algorithm development
? Must have experience with the use of computer tools for simulation
? Must have demonstrated proficiency with C/C++ or C# programming languages
? Strong interpersonal/relationship skills, solid written and verbal communication skills
Additional Desired Skills:
? Proficiency with C#,.Net, Visual Studio, defect tracking, revision control, real-time systems and software/firmware lifecycles. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| R&D Quality Engineer |
| Education Requirements:
Bachelor of Science degree in Reliability, Quality, Mechanical, Electrical Engineering, Math, Physics or equivalent.
Experience Requirements:
Minimum 5 to 10 years experience in Reliability engineering and testing. Medical Device experience preferred.
Ability to interpret, analyze, and present technical information using practical judgement.
Capable of functioning effectively in a team environment.
Proficient in Excel pivot tables and charting.
Excellent written and oral communication skills.
Demonstrated problem solving skills.
Ability to organize and manage concurrent activities.
Knowledge of advanced data gathering and analysis techniques, including statistical analysis.
Knowledge of standard quality and reliability tools such as FMEA (Failure Modes Effect Analysis), Root Cause Analysis, DOE and Statistics.
Proven ability to communicate effectively and manage relationships at all levels of the organization as well as cross-functionally to achieve reliability goal.
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| R&D Quality Engineer |
| Education Requirements:
Bachelor of Science degree in Reliability, Quality, Mechanical, Electrical Engineering, Math, Physics or equivalent.
Experience Requirements:
Minimum 5 to 10 years experience in Reliability engineering and testing. Medical Device experience preferred.
Ability to interpret, analyze, and present technical information using practical judgement.
Capable of functioning effectively in a team environment.
Proficient in Excel pivot tables and charting.
Excellent written and oral communication skills.
Demonstrated problem solving skills.
Ability to organize and manage concurrent activities.
Knowledge of advanced data gathering and analysis techniques, including statistical analysis.
Knowledge of standard quality and reliability tools such as FMEA (Failure Modes Effect Analysis), Root Cause Analysis, DOE and Statistics.
Proven ability to communicate effectively and manage relationships at all levels of the organization as well as cross-functionally to achieve reliability goal.
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| R&D Production Manager |
| This is a managerial position for NMR Cold Probe Production and NPI. The manager is responsible for overseeing the assembly and test of all production cold probes, and coordinating closely with development on specials. The manager will also be responsible for working closely with Cold Probe Development on the smooth introduction of new products into production.
List Minimum education, training and experience needed to perform this job:
1. 15 years experience with NMR probes
2. 5 years minimum supervisory experience
3. familiarity with cryogenic and vacuum systems
4. 10 years manufacturing/production engineer experience |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
9/4/2010
|
| R&D Mechanical Engineer |
| - Bachelors Degree or Masters Degree in ME
- Industry experience as a Mechanical Design Engineer in R&D
- Strong written and verbal communication skills.
- Excellent teamwork skills.
- Self-starter. Willing and able to quickly learn new technologies |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| R&D Manager Advanced Product Development |
| See above |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| R&D Hardware Engineer-Modeling |
| List Minimum education, training and experience needed to perform this job:
1. MS EE or Physics
2. fluent with rf modeling programs
3. fluent with rf measurement tools including network analyzers, spectrum analyzers, noise figure, etc.
4. familiarity with NMR is a plus |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| R&D Hardware Engineer |
| Qualifications:
- Bachelor/Master/PhD Degree in Electrical/Electronic/Computer Engineering with >3 years related working experience
- Knowledgeable in PCIe/modular busses, high-speed digital and memory systems, power integrity, thermal management
- Strong knowledge of digital design with emphasis on ASICs or Xilinx FPGAs
Desired:
- Nano technology/surface science or instrumentation measurement science/domain knowledge
- Strong knowledge of digital and analog hardware, FPGA or digital ASIC development principles, Verilog or VHDL, synthesis, and simulation tools.
- Knowledge of Xilinx ISE, Plan Ahead
- Knowledge of distributed clocking schemes
You will be measured on:
Technical capability and competence and ability to grow and remain technically current
Creativity in designing applicable solutions
Ability to work with a team to deliver results as committed |
| Agilent Technologies, Inc. US |
Everett |
WA |
9/4/2010
|
| R&D Hardware Control Software Engineer |
| This is a key SW development role.
Key Required Skills:
? Bachelors or Masters Degree in Electrical Engineering or Computer Science
? 3+ years applicable experience in software development involving hardware control and IO
? Must have proficiency with C#, C++, .Net, Visual Studio, defect tracking, revision control and software/firmware lifecycles
? Strong interpersonal/relationship skills, solid written and verbal communication skills
Additional Desired Skills:
? Familiarity with Windows device drivers
? Experience with the Windows Presentation Foundation graphical subsystem
? Educational emphasis or work experience with signal processing theory, applications and development |
| Agilent Technologies, Inc. US |
Santa Rosa |
CA |
9/4/2010
|
| R&D FPGA Engineer |
| Key required skills:
? Bachelors or Masters Degree or University Degree in Electrical Engineering and 5+ years applicable experience in FPGA design
? Ability to use FPGA simulation and design tools to realize and verify high quality and robust solutions in Verilog or VHDL.
? Experience with Xilinx ISE, including Plan Ahead, and synthesis tools, such as Synplify
? Ability to perform characterization and testing of design prototypes, and analyze and validate the design to meet product performance specifications.
? Strong interpersonal/relationship skills, solid written and verbal communication skills
Desired skills:
? Educational emphasis or work experience with signal processing theory, applications and development
? Skills in signal processing algorithm development and implementation using FPGAs
? Experience with team-based FPGA development ? design partitioning and integration
? Knowledge in high-speed digital design, PCI Express, DMA, memory systems |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| R&D engineer |
| Qualifications:
- Bachelor/Master/PhD Degree in Electrical/Electronic/Computer Engineering with >5 years related working experience
- Experience with Xilinx ISE, ModelSim, Synplify
- Experience with VHDL or Verilog
- Experience using equipment like oscilloscopes and logic analyzers for problem resolution and design verification
You will be measured on:
Technical capability and competence and ability to grow and remain technically current
Creativity in designing applicable solutions
Ability to work with a team to deliver results as committed |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| R&D Director, Preanalytical Diagnostics |
| See above |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| R&D Bioinformatics, Software Engineer |
| External Qualifications:
This dynamic position requires a MS degree in Computer Science or equivalent plus a minimum of 5+ years relevant experience with bioinformatics tools and procedures as applied to high-throughput computational pipelines.
Chosen candidate must have the following:
? 2+ years of experience in providing bioinformatics solution in next gen sequencing space.
? 5+ years experience in C++, .NET, and Java
? Object oriented programming experience a plus
? Experience with: BLAST, BLAT and/or MOST
? Experience with SQL and/or Oracle database
? Knowledge of public biological databases, tools, and repositories is required
? Hands-on experience producing software in collaborative, multidisciplinary environment to solve problems in biological or other life science is highly desirable
? Experience with Image Analysis is a plus
Geographic Location: Bay Area, California (Santa Clara) |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| R&D Bioinformatics, Senior Software Engineer |
| External Qualifications:
This dynamic position requires a MS degree in Computer Science or equivalent plus a minimum of 5+ years relevant experience with bioinformatics tools and procedures as applied to high-throughput computational pipelines.
Chosen candidate must have the following:
? 5+ years experience in C++, .NET, and Java
? Object oriented programming experience a plus
? Experience with: BLAST, BLAT and/or MOST
? Experience with SQL and/or Oracle database
? Knowledge of public biological databases, tools, and repositories is required
? Hands-on experience producing software in collaborative, multidisciplinary environment to solve problems in biological or other life science is highly desirable
? Experience with Image Analysis is a plus
Geographic Location: Bay Area, California (Santa Clara) |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
9/4/2010
|
| R&D ASIC Engineer |
| Minimum Qualifications:
BS or MS in Electrical Engineering or Computer Engineering
? Exposure digital VLSI design
? Demonstrated Verilog/System-verilog design
? Knowledge of semiconductor devices and structures
? Understanding of physical implementation
? Understanding of analog design basics
? Understanding of digital ASIC design methods, tools and verification methodologies
? Understanding of physical VLSI ASIC design methods and tools
? Strong multi-tasking and teamwork skills
? Strong verbal and written communication skills
? Ability to understand systems and digital architectures
? Strong understanding of engineering mathematics |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Quantitative Mass Spectrometry Research Associate (BS/MS) |
| BS/MS in biology or chemistry with a minimum of two years experience with compound quantitation using triple quadrupole mass spectrometers; No experience in proteomics mass spectrometry required; In-depth knowledge and hands-on experience with LC/MS of compounds or peptides; Direct experience with operation, maintenance, and troubleshooting of triple quadrupole mass spectrometers; Extensive experience with compound or peptide quantitation using SRM/MRM and internal standards. |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Quality Specialist, Quality Systems |
| * B.S. in a scientific or allied health field (or equivalent degree) and 3 ? 5 years of relevant work experience
* Has provide Instructor-led training on various GxP topics as needed
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Quality Management Principal Engineer - Instruments |
| See above |
| Novartis Oncology |
na |
CA |
9/4/2010
|
| Quality Control Scientist |
| BS in Micro Biological Science or equivalent discipline. Minimum of 5-7 years of related experience or equivalent. Thorough knowledge of chemical, microbiological, and EM test methods. Proficient in performing benchtop microbiology techniques. Thorough knowledge of GMPs/GLPs. Strong communication skills. Requires handling of chemicals such as acids, alkalis, solvents and powdered media; Work with biohazardous agents such as E. coli or S. cerevisiae; Requires bending and reaching throughout the work shift in support of wide range of activities such as valve adjustment, fastening of hoses and/or connections and conducting cleaning activities; Requires walking / standing for extended periods (up to 6 hours) throughout the work shift; May require dexterity for fine motor tasks such as pipetting and sterile manipulations in biosafety cabinets (periods up to 2 hours); May need to adapt to changing work shifts, both swing and/or graveyard on very short notice; May use a computer for greater than 4 hours a day. |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
9/3/2010
|
| Quality Control Microbiology Technician |
| See above |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Quality Control Microbiologist - Agensys, Santa Monica, CA |
| ? A Bachelor?s degree or equivalent work experience in microbiology or science discipline. Must have 1 ? 2 years experience in a GMP Microbiology pharmaceutical or biopharmaceutical environment. Familiarity with cGMP manufacturing a plus.? Must have strong teamwork and organizational skills ? Resourceful, self-reliant, self-motivated, and confident ? Excellent verbal and written communication skills ? The ability to multitask and exercise good judgment ? Detailed oriented with good follow-up skills ? Assist with administrative tasks related to the department ? Maintains good aseptic technique, housekeeping, order, and safety in the laboratory? Maintain logbooks, record and report all test results in a timely manner ? Revise procedures as necessary to improve efficiency and ensure compliance with regulatory requirements ? Must be familiar with Microsoft Word and Excel |
| GE Healthcare |
Northampton |
MA |
9/3/2010
|
| Quality Control Manager |
|
1. Bachelor?s degree (or high school diploma/GED plus 4 years of related work experience)
* At least 3 years of experience working in one of the following areas: regulated medical device, regulated pharmaceutical environment, quality control/assurance, or regulatory assurance
* At least 1 year of management experience to include direct reports
* Ability to effectively communicate using English (or local language)
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
* Demonstrated managerial experience
* Bachelors of Science in a related discipline (electronics, mechanics, thermodynamics, biochemistry)
* Leadership and motivational skills
* Organizational skills
* Fine attention to Detail
|
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Quality Control Analytical Lab Supervisor |
| Minimum Education and Experience Requirements:
Requires a Bachelors degree in Chemistry or related science from and accredited college or university with a minimum of 7 years of experience overall with 5 years supervisory experience in a regulated laboratory, preferably in a pharmaceutical laboratory environment.
Requires solid knowledge of quality control systems, including FDA compliance standards, regulations, and guidelines.
Requires excellent oral and written communication, organizational and teamwork skills.
n equivalent combination of education, experience and training may substitute.
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
9/3/2010
|
| Quality Assurance Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
9/3/2010
|
| Quality Assurance Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
9/3/2010
|
| Quality Assurance Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| QM Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
9/3/2010
|
| QC Associate I - BDB |
| See above |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| QA Document Specialist - Agensys, Santa Monica, CA |
| ? 2-5 years in cGMP experience preferred? BA or BS Degree in Life Sciences preferred? Proficient computer skills in Microsoft Word, Excel, and PowerPoint. MS Access experience is a plus.? Quality Assurance controlled document experience recommended.? Detail oriented and able to work effectively independent of direct daily supervision? Strong oral and written communication skills required? Flexible and fast learning team player. ? Organized and able to multi-task in a fast-paced environment. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| QA Associate I - Agensys, Santa Monica, CA |
| ? Minimum 3-5 years GMP experience required? BA or BS Degree in Life Sciences or 5-7 years of professional GMP experience? Previous Quality Assurance signature approval of controlled documents required? Strong computer skills recommended, experience with Access / Trackwise highly desirable? Strong oral and written communication skills required? Experience reviewing, creating, and implementing Standard Operating Procedures preferred? Experience with equipment validations preferred |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| PTM (Project Team Member), Strategic Marketing, GPS |
| University degree in Medicine, Biological or Pharmaceutical Sciences. An advanced degree in bioscience, and/or business is a plus (e.g., MD, Pharm. D., PhD., MBA)
Strong science and business background
? Excellent understanding of Oncology market
? Extensive contact with Oncology/Hematology Medical experts
? Proven ability to operate and influence cross-functionally and cross culturally
? Proven leadership ability
? Strong analytical and strategic thinking skills
? Oncology product development experience
? Significant experience in launching new products |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Proteomics and Mass Spectrometry Scientist (BS/MS) |
| BS/MS in biology or chemistry with >5 years experience in a mass spectrometry laboratory. In-depth knowledge and hands-on experience with LC/MSMS and ESI of proteins and peptides. Excellent communication skills and the ability to multitask in a fast-paced environment are essential.
Experience in cell biology or cell culture is a plus. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Protein NMR/Biophysics Research Associate (BS/MS) |
| B.S/M.S. or equivalent in biochemistry or a related discipline with at least 2 years of research laboratory experience. Experience in protein handling/characterization and laboratory automation is required. Attention to detail, an ability to work independently, and multitasking skills are expected. Experience with NMR spectroscopy and/or biophysical characterization of proteins and computational skills would be a decided asset. The candidate must possess good oral and written communication skills and should be able to function well in a matrix managed environment. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Protein Biochemistry Research Associate (BS/MS) |
| B.S/M.S or equivalent in biochemistry or a related discipline with at least 2-3 years of research laboratory experience. A strong background in protein expression and purification is highly desirable. Molecular biology experience is also an important pre-requisite. Must be detail oriented and be able to handle multiple tasks efficiently. The candidate must possess good communication skills and be comfortable working in a matrix based team environment. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Protein Biochemistry Research Associate (BS/MS) |
| B.S/M.S or equivalent in biochemistry or a related discipline with at least 5 years of research laboratory experience. A strong background in protein expression and purification is highly desirable.
The successful candidate will be expected to be able to participate in experimental design and to independently conduct experiments. They must also be detail oriented and be able to handle multiple tasks efficiently. The candidate must possess good communication skills and be comfortable working in a matrix based team environment. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Protein Biochemistry Research Associate (BS/MS) |
| B.S/M.S or equivalent in biochemistry or a related discipline with at least 2-3 years of research laboratory experience. A strong background in protein expression and purification is highly desirable. PhD level scientists should not apply.
The successful candidate will be expected to be able to participate in experimental design and to independently conduct experiments. They must also be detail oriented and be able to handle multiple tasks efficiently. The candidate must possess good communication skills and be comfortable working in a matrix based team environment. |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Project Statistician |
| See above |
| BD (Becton, Dickinson and Company) |
Miami |
FL |
9/3/2010
|
| Project Scientist |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Project Manager/System Engineer |
| See above |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Project Manager/Senior Project Manager, DDPM |
| Bachelors Degree required. Advanced degree (masters, doctorate) a plus. Generally, five (5) years with Masters Degree or seven plus (7+) years relevant experience with a minimum of three to five (3-5) years experience directly related to drug development process with a demonstrated understanding of the drug development process, and project management skills required. Knowledge of required CMC, pharmacology, toxicology, PK, clinical requirements to support major US regulatory filings ? IND, NDA, etc.Demonstrated expertise /discipline in project management and a key organizer who has shown to set clear priorities on developmental activities, with experience in planning systems (e.g. MSProject) and an understanding of financial planning / expenditures. Good communication, people management and social skills with a good sense of diplomacy both in a scientific and industrial environment.Effectively utilizes information technology systems and provisional project management tools.Capable of managing meetings within a multicultural environment and organize expert meetings with KOLs. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Project Management Specialist - Agensys, Santa Monica, CA |
| The ideal candidate will have a university degree and a minimum of 5 ? 8 years related experience in Project Management or in Drug Development ? preferably both. Even more preferable would be Drug development project management experience in biologics or biologic-based drugs. Working knowledge of PM tools such as MS Project and MS Excel is required. Experience in initiating and implementing additional communication, planning, scheduling and development strategy software tools are a plus. Excellent communication skills and the ability to work in a team environment are essential. PMP certification a plus but not essential |
| GE Healthcare |
Westborough |
MA |
9/3/2010
|
| Project Leader, Black Belt |
|
Education/Knowledge:
* Degree in Mechanical engineering, plastics engineering, or a related field
* BS with a min of 10 years relevant industry experience or MS with a min. of 6 years of relevant industry experience
* Strong analytical and quantitative statistical skills; facility with Six Sigma concepts and tools
* Working understanding of regulatory issues related to Biopharmaceutical manufacturing and licensure related to medical devices
Skills:
* Negotiation, communication, presentation and listening skills
* Fluency in written and spoken English
Standard Microsoft Office packages and statistical software
Basic project management
Experience:
Work in a regulated environment (e.g., GMP or ISO quality system)
Other:
Authorization to work in the USA
Ability to travel domestically and internationally on an occasional basis
Ability to perform physical tasks that require mobility, manual dexterity, and visual acuity
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
* Change agent with strong credibility and influence in the organization
* Masters degree in business related field
* Demonstrated ability to motivate others and achieve results
* Demonstrated commitment for process improvement and product quality
* Customer-focused in defining quality and establishing priorities
Strong oral and written communication skills
Strong interpersonal and leadership skills
Executive level presentation skills
|
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Project Engineer R&D |
| See above |
| BD (Becton, Dickinson and Company) |
Broken Bow |
NE |
9/3/2010
|
| Project Engineer |
| See above |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Project Data Manager |
Education/Experience Qualified candidates must have a Bachelor's degree or Registered Nurse with a minimum of 6 years pharmaceutical/data management experience or a Master's degree plus a minimum of 4 years experience in pharmaceutical/data management. Project management experience is preferred. Clinical database administration and system validation experience; CRO management experience; and demonstrated knowledge of clinical data flow and research design are critical skills in this role. |
| Daiichi Sankyo, Inc. |
Edison |
NJ |
9/3/2010
|
| Project Data Manager |
Education/Experience Qualified canddiates must have a Master's degree; Bachelors degree or registered nurse in life sciences; 4 to 6 years (MS) pharmaceutical/data management; 6 to 8 years (BS/RN) pharmaceutical/data management. Project management experience is preferred. Demonstrated knowledge of clinical data flow and research design; clinical database administration and system validation experience; demonstrated competence with GCP/regional regulatory guidelines, SOPs (including WPs), medical terminology, standard coding dictionaries, and demonstrated proficiency in applying them to all relevant therapeutic areas and CRO management experience, including a thorough knowledge of CRO audits are critical skills in this role. EDC and SDTM experience is preferred. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Program Section Leader (MD) Thrombosis |
| Education (minimum/desirable):
MD, required
Advanced knowledge in medical/scientific area required.
Languages:
Fluent oral and written English.
Experience/Professional requirement:
? ?8 years of involvement in drug development spanning clinical activities in Phases II/IV or comparable experience in industry.
? ?4 years of demonstrated leadership and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing), or section of clinical programs in a global/matrix environment (including remote) in pharmaceutical industry.
? ?4 years people management experience required, this may include management in a matrix environment. Global people management experience desirable.
? Strong management, interpersonal, communication, negotiation and problem solving skills.
? Considerable organization awareness (e.g., inter-relationship of departments, business priorities), including significant experience working cross-functionally and in global teams.
? Medical/scientific and operational expertise appropriate to the program. |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Program Manager, Exploratory Development and Lab Solutions |
| Minimum Education Requirements:
? BS/BA in a Science Field ? Chemistry, Biology, etc..
? A degree or related experience in an Information Systems or Computer Science field is a plus
Minimum Experience Requirement:
? Previous experience working in a Pharmaceutical Research environment
? Minimum 5 years defining, implementing, and supporting Research, Discovery and Lab Systems.
? Minimum 5 years in a Project Management role or equivalent role
? Part of an IS team that has been responsible for developing a strong product pipeline
? Consulting experience in working with Research and Discovery or Clinical solutions a plus
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Agilent Technologies, Inc. US |
Columbia |
MD |
9/4/2010
|
| Program Manager |
| ? Bachelors or Masters Degree in Electrical Engineering or Computer Science or equivalent experience.
? Ten or more years experiance in the industry with five or more years as a Program/Project Manager
? Background in Wireless or IP networking preferred.
? Experience executing DoD programs throughout a milestone-oriented program life cycle.
? Track record of delivering quality solutions on time and delighting customers
? Mastery of Microsoft Project, Excel, Word, and Outlook
? Experience in new product, or novel system, development processes (e.g., software or hardware) as well as experience with life cycle support processes.
? Proven ability to work in a team, gain alignment among customers, teams, peers, partners, and management
? Proven ability to adapt to changing requirements in response to pressing customer needs
? Proven ability to prioritize and balance resources across multiple projects
? Experience with leading, planning, organizing, tracking and reporting for project teams and tasks
? Meticulously attentive to detail
? Experience with mentoring, staffing, and people development.
? PM Certification a plus, but not required. (Experience counts for more.)
? US Citizen with, or capable of obtaining, a high level security clearance. |
| Novartis Oncology |
na |
TX |
9/4/2010
|
| Professional Services Vet-Cattle |
| ? DVM or equivalent
? 5 years with Novartis Animal Health with consistently high performance ratings or 7 years or more professional experience with listed qualifications
? Advanced degree in medical specialty, practice management or business administration encouraged
? Marketing/Sales Management experience |
| Astellas Pharma, Inc. |
Bridgeport (1P010207) |
CT |
9/3/2010
|
| Professional Representative PCP- Bridgeport, CT |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Philadelphia North (1P010604) |
PA |
9/3/2010
|
| Professional Representative PCP - Philadelphia North, PA |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Extensive travel is required for this position- Some experience (1 year) with business-to-business sales If you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| BD (Becton, Dickinson and Company) |
Broken Bow |
NE |
9/3/2010
|
| Production Shift Facilitator - 12 hr shift - Blue Nights |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
9/3/2010
|
| Production Planner II |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Production Operator IV |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Production Operator III |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Production Operator III |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Production Operator II |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Production Operator II |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Production Operator II |
| See above |
| Agilent Technologies, Inc. US |
Cary |
NC |
9/4/2010
|
| Production Manufacturing Supervisor |
| ? Will have a bachelor?s degree in a technical or operational field.
? Will have a minimum of five years of experience as supervisor preferably in high precision technology product manufacturing.
? Extensive knowledge of lean manufacturing process activities and quality management system requirements.
? Proficiency with SAP or other ERP systems and Microsoft Office Applications.
? Proficiency in verbal and written English. |
| GE Healthcare |
na |
CA |
9/3/2010
|
| Product Specialist ? Filtration and Single-Use |
|
* This is a home office based sales position and as such the candidate must reside within their territory in order to support this role.
* Bachelor?s degree in chemical engineering or mechanical engineering.
* 3+ years of hands-on experience with BioProcess filtration and/or fluid-handling technologies
* Excellent oral presentation and technical writing skills.
* Overnight travel, up to 50%, is required.
To the extent that you are applying for a position that requires you to operate a GE owned/leased, privately owned/leased or rental vehicle for company business, you must have a valid drivers license and be willing to submit to a check of your driving records.
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
* Working knowledge of UNICORN
* Hands-on experience in process development for sizing and optimizing filtration processes
* Strong background in the use of single-use products for normal-flow filtration, cross-flow filtration and fluid handling.
* Technical sales or sales support experience or direct employment in a biotech or pharmaceutical production or process development environment.
* This position requires a high degree of self-motivation and prioritization skills. The candidate must also have a talent for getting along with and working productively with a variety of highly motivated sales personalities.
|
| Shimadzu Scientific Instruments, Inc. |
Columbia |
MD |
9/3/2010
|
| Product Specialist - Liquid Chromatography |
| Incumbent must be proficient at effectively troubleshooting operational, application and other instrument problems in a methodical efficient manner. Additionally, incumbent must be able to act independently in matters not governed by policy to ensure customer satisfaction. Incumbent must have a Bachelor’s degree in the physical or natural sciences with at least two years of technical applications experience in the appropriate product line (HPLC) or the equivalent experience in maintenance and/or repair of analytical instrumentation.
Please visit our website for a complete job description and to use our apply online feature - www.ssi.shimadzu.com/employment.
SSI is an EOE -M/F/D/V |
| Agilent Technologies, Inc. US |
Indianapolis |
IN |
9/4/2010
|
| Product Specialist - Columns and Supplies - Midwest |
| - BS Degree in Science (Chemistry/Biology) or equivalent
- 8+ years progressive experience in chromatography applications and/or sales along with a demonstrated track record of results preferred.
- Proven ability to understand customer needs and identify solutions to non-standard tasks/queries; actively creates business opportunities.
- Ability to solve a broad range of problems of varying scope and complexity.
- Excellent communication and teamwork skills is a must.
Geo Location: Midwest Area |
| Agilent Technologies, Inc. US |
Wilmington |
DE |
9/4/2010
|
| Product Specialist - Columns and Supplies - Mid Atlantic |
| - BS Degree in Science (Chemistry/Biology) or equivalent
- 4+ years progressive experience in chromatography applications and/or sales along with a demonstrated track record of results preferred.
- Proven ability to understand customer needs and identify solutions to non-standard tasks/queries; actively creates business opportunities.
- Ability to solve a broad range of problems of varying scope and complexity.
- Excellent communication and teamwork skills is a must.
Geo Location: Mid Atlantic Area |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Product Safety Specialist |
| Minimum Experience Required:
1-2 years experience within contact lens or medical device industry within one of the following functions: manufacturing, quality affairs, customer service, or product consultation
Preferred Level:
3-5 years complaint handling, adverse event reporting or product quality risk in a medical or pharmaceutical regulated environment.
2 years experience dealing with healthcare professionals and/or consumers.
Ability to work independently in fast-paced environment with little supervision.
Detail oriented, and ability to multitask.
Computer literacy with Microsoft Office,Lotus Notes and Trackwise.
Excellent written and verbal communication skills are essential
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Agilent Technologies, Inc. US |
Chandler |
AZ |
9/4/2010
|
| Product Marketing Engineer |
| - Bachelor degree in relevant science or engineering discipline; Ph.D. strongly preferred (e.g. Material Science, Life Sciences, Chemistry, Physics, Biology or Biophysics)
- 5+ years recent experience applying scanning electron microscopy to scientific, industrial and/or manufacturing problems; understanding of electron-specimen interactions
- Exceptional written and verbal communication skills; Ability to address a diverse audience is critical to the successful candidate
- Versatile interpersonal skills to communicate across geographies, cultures, organizational functions.
- Domestic and international travel required
- Ability to speak a second language highly desirable
Geo Location: Chandler, AZ |
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Product Manager/Sr Product Manager |
|
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Product Manager - Software |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
9/3/2010
|
| Product Manager - Reagents |
| See above |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Product Manager - Genomics |
| Requires:
- BS in biology, biochemistry, molecular biology; related discipline or equivalent. Master or PhD preferred.
- 5+ years experience in marketing life science products.
- Demonstrated use of marketing skills and market knowledge to define and commercialize products that result in business success
- Experience in working with worldwide customers and is a strong advocate for customer focus and customer driven development
- Demonstrate ability to develop marketing plans that align with strategic objectives
- Ability to work independently to plan, prioritize workload, schedule time, assess and solve problems
- High proficiency in pricing and forecasting
- Must exhibit strategic thinking, teamwork, creativity, planning and organization, and flexibility
- Strong analytical and decision making skills
- Experience in working with global markets/customers an advantage
- Excellent written and oral communications skills and comfortable presenting to high level audiences both internally and externally
- Must have flexibility in working hours and available for 25% business travel
Geographic Location: Santa Clara, California. |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Product Manager - Cell Culture Environment |
| See above |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Product Manager |
| Educated to at least university degree level or equivalent, you'll bring at least 9 years' practical experience, through which you'll developed an in-depth knowledge of market and channel distribution mechanisms. This is where your specialist knowledge, technical leadership and customer-focused, solutions-oriented approach will thrive.
Geo Location: Santa Clara, CA |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Product Manager |
| See above |
| Shimadzu Scientific Instruments, Inc. |
Columbia |
MD |
9/4/2010
|
| Product Coordinator/Molecular Spectroscopist |
| Incumbent must be proficient at effectively troubleshooting operational, application and other instrument problems in a methodical efficient manner. Additionally, incumbent must be able to act independently in matters not governed by policy to ensure customer satisfaction. Incumbent must have a Bachelor’s degree in the physical or natural sciences with at least seven years of technical applications experience in the appropriate product line or the equivalent experience in maintenance and/or repair of analytical instrumentation. |
| Novartis Oncology |
na |
NC |
9/4/2010
|
| Procurement/Sourcing Manager |
| Bachelor?s degree required at a minimum, master?s degree preferred in fields such as Supply Management, or a scientific or technical field. Strong preference for CIPS or similar professional qualification.
5-10 years of Procurement experience in a pharmaceutical manufacturing or regulated (GMP) product environment. Extensive experience in category and demand management, collaborative cost reduction and productivity programs, activity-based cost analysis, and negotiation. Technical experience with pharmaceutical chemicals and associated materials. |
| Agilent Technologies, Inc. US |
Anaheim |
CA |
9/4/2010
|
| Procurement Supervisor |
| *A Bachelors Degree plus 6 years of relevant work experience from an accredited University OR equivalent experience.
*2-5 years working knowledge of SAP is a must
*Knowledge of Medical Device or Diagnostics a plus
*Experience working in an FDA approved facility
You'll enjoy all the support and encouragement you need to grow your skills and knowledge base. If you can bring some experience, great. Your positive, proactive attitude and willingness to work as part of a go-getting team are what will set you apart.
GEOGRAPHIC LOCATION: Lake Forest, CA
No sponsorship or relocation provided for this role. |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
9/3/2010
|
| Process Technician |
| See above |
| BD (Becton, Dickinson and Company) |
Madison |
WI |
9/3/2010
|
| Process Technician |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
9/3/2010
|
| Process Technician |
| See above |
| Novartis Oncology |
na |
NE |
9/4/2010
|
| Process Engineer |
| Required: BS degree in an appropriate scientific, pharmaceutical or engineering discipline and 3 to 5 years of demonstrated experience in pharmaceutical formulation, packaging engineering, and/or process development. Experience with pharmaceutical production practices, manufacturing and packaging equipment, and instrumentation and controls. Working knowledge of GxPs. Demonstrated ability to execute facility, process, computerized system, cleaning, and equipment validations.
Preferred: Packaging Engineer or Electrical Engineer with advanced degree. Prior accomplishments in pharmaceutical formulation, development for various dosage forms, or packaging engineering in relevant environments. Prior experience executing capital projects. Working knowledge of analytical testing preferred; demonstrated experience with quality engineering methodology desired.
Only on-line resumes will be accepted.
If you require accommodation under the American?s with Disabilities Act to apply for this position,
contact Suzanne Drew (402) 467-8808. |
| Regeneron Pharmaceuticals, Inc. |
|
|
9/4/2010
|
| Process Development Engineer |
| The ideal candidate will have a Bachelors or Masters degree in Chemical Engineering with a concentration in biochemistry and 0 - 5 years experience in the biotech or pharmaceutical industry. Knowledge and experience with bioseparations processes is preferred.
|
| BD (Becton, Dickinson and Company) |
Columbus West |
NE |
9/3/2010
|
| Process and Automation Development Engineer-PosiFlush |
| See above |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Principle Medical Scientific Expert MD (CV) |
| Education:
? MD with unique knowledge for successful clinical program development and execution, with ? 3 years of clinical research experience required. Preference for 2+ years of industry experience
Or
? MD with specialty with board certification or equivalent required.
Languages:
Fluent English (oral and written)
Experience:
? Advanced medical/scientific writing and communication skills.
? Proven ability to interpret, discuss and represent efficacy and safety data relating to the assigned area (Cardiovascular)
? Proven ability to work both independently or in a cross functional team setting, including a matrix environment.
? Demonstrated ability to establish effective working relationship with key investigators in assigned TA (CV).
? Medical and/or scientific expertise within the Cardiovascular disease area. |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Principal Statistical Programmer |
| * B.S. in Biostatistics, Statistics, Computer Science, or a related field and a minimum of 10 years of SAS and relevant pharmaceutical industry experience
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Principal Scientist, Preformulation |
| Education & Experience
14-19 Years with Bachelors of Science, 12-17 years with Master of Science, 9-14 years with PhD |
| Teva Pharmaceuticals USA |
Irvine |
CA |
9/4/2010
|
| Principal Scientist I - Preformulation/Formulation Group Leader |
|
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Principal Scientist - Salt and Polymorphism Expert |
| Education (minimum/desirable):
Minimum: BS/MS organic/analytical chemistry with 7-10 years of experience in solid state chemistry of APIs.
Desirable: Ph.D. organic/analytical chemistry or equivalent education with strong emphasis on solid state chemistry with 3-5 years of experience in pharmaceutical industry (knowledge of molecular modeling and GMPs would be a plus). Experience with form selection, polymorphism, and physicochemical characterization of APIs. Familiarity with current analytical instrumentation and techniques to characterize API forms using FBRM, XRPD, DSC, TGA, vibrational spectroscopy, UV-Vis, vapor sorption, GC, HPLC, size and solubility measurement, with an emphasis on laboratory automation. Excellent written and verbal communication skills. Good project management, time management, and decision making skills.
Languages: Fluent English (oral and written)
Experience/Professional requirement:
1. Successfully demonstrated several years (minimum of 3 years)of directly related experience as senior scientist or equivalent in pharmaceutical R&D.
2. Documented scientific/technical expertise in form selection, polymorphism, and characterization of APIs.
3. Successfully demonstrated track record of creativity and problem solving in projects.
4. Proven track record in utilization of special tools/equipment, lab automation tools and specialized facilities.
5. Profound literature search skills.
6. Strong presentation skills and scientific/technical writing skills.
7. Proven scientific leadership skills.
8. Ability to work in interdisciplinary teams.
9. Familiarity with the current analytical instrumentation and techniques to characterize crystalline and amorphous materials.
10. Familiarity with GLPs as applied to pharmaceutical industry. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Principal Scientist - Formulation |
| Education
Mminimum: Technician with continuing education (EU) or BS/MS or equivalent.
Desirable: Advanced degree in a scientific or relevant discipline (Ph.D. or equivalent).
Languages: Good knowledge of English (oral and written). Desirable knowledge of site language.
Experience/Professional requirement:
1. Successfully demonstrated several years (minimum of 3 years) of directly related experience as Senior Scientist or Ph.D. with post-doctoral/industrial experience (minimum of 1 year) or equivalent.
2. Successfully demonstrated expertise in a specific scientific/technical area.
3. Recognized achievements in the development of new lab/plant procedures.
4. Excellent knowledge of laboratory and/or technical tools.
5. Proficient in utilization of special tools/equipment, lab automation tools and specialized facilities e.g., containment/sterile labs.
6. Thorough understanding of development activities and processes in a specific function.
7. Good knowledge of software and computer tools.
8. Profound literature search skills.
9. Good presentation skills and scientific/technical writing skills.
10. Strong scientific leadership skills.
11. Strong knowledge of relevant SOP, GLP, GMP and Novartis regulations and policies.
12. Very good communication skills, advanced coaching skills.
13. May require up to 15% travel.
Experience with drug delivery technologies and application to solid dosage forms preferred. |
| AstraZeneca Pharmaceuticals |
Waltham |
MA |
9/4/2010
|
| Principal Scientist - Cell/Lead Biologist |
| Minimum Requirements
*PhD and 5+ years experience in cancer cell biology with a minimum of 3 years in the pharmaceutical industry or equivalent
Competencies/Behaviors
*Strong understanding of cell assay development and small molecule drug screening
*Broad understanding of cancer disease biology
*Demonstrated previous authorship of patents and/or peer reviewed publications
*Ability to work in a team-oriented environment
*Strong interpersonal and communication skills
*Effective leadership and management skills
*Delivery focused |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
9/3/2010
|
| Principal Polymer Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Principal Engineer- Pen Injection Platform |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Principal Engineer, Mechanical/Environmental</ |
