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  1. Quality Control Specialist 1 – Full Time

      DESCRIPTION: Perform bioassay analytical testing of various biological drug substances, drug products and other materials including cell-based bioassays, ELISAs and gel assays according to approval methodologies.  Responsible for following all appropriate SOPs, methods, policies and safety guidelines and training of other QC analysts as requested.  Prepare reagents, samples and equipment according to SOP and maintain instrumentation and lab facilities.  Responsible for completing and ...

  2. Quality Control Stability Senior Analyst/Specialist – Full Time

      DESCRIPTION: Help set up stability studies for pharmaceutical products, evaluate stability data and draft stability reports under the direction of the Stability Manager.  Responsible for following all appropriate SOPs, methods, policies and safety guidelines and training of other QC analysts as requested.  Responsible for completing and reviewing laboratory documentation in a cGMP compliant manner and will also help review and approve laboratory data. Reports to the QC Stability Manager. ...

  3. Senior Quality Control Analyst – Full Time

      DESCRIPTION: Perform analytical testing of various drug substances, drug products and other materials according to approved methodologies using HPLC, GC and other techniques.  Responsible for following all appropriate SOPs, methods, policies and safety guidelines and training of other QC analysts as requested.  Prepare reagent, samples and equipment according to SOP and maintain instrumentation and lab facilities.  Responsible for completing and reviewing laboratory documentation in a cGMP ...

  4. Associate Director Biostatistics - Oncology - SF Peninsula

    The Associate Director, Biostatistics provides expert biostatistics support for the planning, design, conduct, analysis and reporting of clinical studies.  Ideal candidate will have 8+ years of pharma/ biotech experience, a Ph.D. and experience working Oncology clinical trials.  Responsibilities include the statistical design of Phase I - IV clinical studies (specification of study hypotheses, sample size estimation and power calculations), the statistical delineation of study endpoints, writing ...

  5. Statistical Programmer / SAS / Clinical - SF Bay Area - contract / FTE

    Our San Francisco Peninsula Client has a need for both full time and a contract SAS Programmer,  the ideal candidate will provide statistical programming support and validation of analysis datasets, create statistical tables, graphs and listings for clinical trial data and assist in developing software to support project teams analysis requirements.  CDISC experience (i.​e.​ SDTM & ADaM) desireable.  Qualified applicants must have minimum of 5 years of SAS programming in a pharmaceutical/biotech/CRO ...

  6. Hiring a Sr. Statistical Programmer in San Francisco!

    Ref#: 119408 Job Title: Sr. Statistical Programmer Analyst City/State: San Francisco, CA   Job Description:  Department - Biometrics and Data Management Job Title - Sr. Statistical Programmer Analyst Education - A minimum of a Bachelor's degree in Computer Science, Mathematics, Statistics, and related areas is required. A Masters or PhD is preferred. Equivalent experience may be accepted. A minimum 8 years hands on relevant career experience in the pharmaceutical or biotechnology industry.  ...

  7. Interviewer/Phlebotomist - 1403

    LOCATION: San Francisco   This is a field based, regular part-time (up to 36 hours) position with benefits.   What you do in your career can positively affect 1 out of every 2 people. You can join a dedicated group of people who connect with a valued mission to prevent cancer and to reduce its burden where it cannot yet be prevented. The Cancer Prevention Institute of California (CPIC) is looking for a Interviewer/Phlebotomist. PURPOSE OF POSITION: To recruit eligible subjects to participate ...

  8. QA Analyst I

    Job Title:QA Analyst I Duties: Follow company policies and procedures. Maintain a state of inspection readiness. Provide input to the development of personal performance goals and departmental objectives. Collaborate with Management to establish and meet targets and timelines. Independently manage competing priorities with limited instruction. Serve as a Quality representative on cross-functional and multi-site teams. Identify and recommend solutions to potential procedure, process and ...

  9. Engineering Manager (large scale wet chemistry) (VS)

    WHEN WE RECEIVE YOUR RESUME, WE WILL SEND YOU A COURSE ON HOW TO BECOME AN INTERVIEW SUPERSTAR. IT IS FREE BUT IF WE CHARGED THOUSANDS IT WOULD BE WORTH IT.   Engineering Manager (large scale wet chemistry) (VS) Pharmaceutical / Biotech Engineering - Chemical Full-time United States - California - Silicon Valley/San Jose - Santa Clara  ID - 883826 The Compensation Benefits - Full Bonus Eligible - Yes Interview Travel Reimbursed - Yes Detailed Job Description Join the Microarray Fab organization ...

  10. Manufacturing Bioprocess Technician

    Job Title:MFG BioProcess Technician Number of Positions:2   Remaining Positions:2   Duties: Support the Manufacturing department by working effectively to meet department goals, objectives and tasks to achieve desired results. Responsible for completing assigned tasks which include cleaning, sterilizing, and prepping glassware and parts used in the manufacturing environment. Work with senior technicians and leads to prioritize tasks and assignments and make recommendations to maximize efficiency ...

  11. Clinical Associate #TMS3894746

    Clinical Associate needed for large biotech firm in Foster City, CA. Pay is $36.00/hour, fulltime hours, W-2.  One year contract.  Please apply if interested.  Duties               Perform design verification and analytical validation studies in the lab for IVD products. Generate test protocols, review and analyze results, and generate V&V reports per FDA and ISO regulation. Maintain proper ISO and FDA QSR documentation and implementation. Support to Transfer molecular IVD assays from R&D into ...

  12. Associate Scientist I - R&D, #TMS3909093

    Associate Scientist I position open at large biotech company in South San Francisco, CA.  Pay is $24.00/hour,1 year contract, fulltime hours, W-2.  See full job description below. Duties              Conduct pre-designed scientific or engineering experiments using laboratory equipment and calculations. Verify and validate product design and performance during the development cycle, from feasibility through product release.  Products include bench top instruments, sample preparation, synthetic ...

  13. Sr. Biostatistician/ contract/ SF Peninsula & East Bay

    ~~Our Bay Area Clients have asked us to locate, qualify and present a Sr. Biostatistician for a long term contract. Key Accountabilities/Core Job Responsibilities: • Collaboration with clinical scientists on protocol design (author statistical methods section and generate study randomization) • Generate statistical analysis plan for assigned protocols (incl. Mock displays) • Assume responsibility for individual studies, write statistical portion of integrated clinical/statistical reports • Work ...

  14. Systems & Verification Engineer – Relocation Assistance

    IVD Systems & Verification Engineer – Full Time Position DESCRIPTION: Work closely with marketing to develop product requirements. Work closely with other senior technical staff to identify the key technical challenges to meeting said requirements, and develop system architectures for IVD products. Improve on the process for system and sub-system verification, including test automation and traceability to requirements, specifications and risk. Partake in verification and validation testing as ...

  15. Rubber Compounding Chemist

      Throughout their 57 year history, our valued client has continued to recognize that their people are their greatest strength!  This has meant continued success which prompted them to direct us to identify an experienced rubber compounding chemist as further described below. Don't delay. Apply now! Your professional background and contacts suggest you may be able to assist in this crucial, active search. Permanent Employment Opportunity Announcement      Chemist (Job #6581) Location -      San ...

  16. CRA I /II – Full Time

    DESCRIPTION: Responsible for implementing and monitoring clinical trials and expands experience in clinical trial and vendor management procedures.  Works closely with study coordinators and investigators to ensure compliance with protocol and overall clinical objectives. Identifies projects/tasks and works with Clinical Trial Manager to complete.  Demonstrates ability to carry out all CRA I functions with minimal supervision.  In collaboration with manager and/or Lead CRA, maintains ...

  17. Clinical Trial Mgr / CTM III / Full Time / SF Bay Area

    Our San Francisco Bay Area client has asked us to locate, qualify and present a Clinical Trial Manager with 5 years of experience (2 yrs oncology).  Candidate will be responsible for and/or assisting with the execution of Investigator-Sponsored Trials and Client-sponsored hematological clinical trials from protocol concept through clinical study report. Primary Responsibilities and Duties:•Coordinate with investigators and investigator sites . •Coordinate and/or participate in investigator meetings ...

  18. Sr. Clinical Data Manager (CDM) / Oncology/  Full time / SF Bay Area

    Sr. Clinical Data Mgr / Oncology / Full Time / SF Bay Area Close to BART $125K to $140K - DOE Our San Francisco Bay Area Client has asked us to locate, qualify and present a Sr. Clinical Data Manager for a full time position. This is a lead (SENIOR) role which will allow you to oversee the process from start up to close out.  You will create written data management plans and help design database structures and CRFs.   Experience with Clintrial is helpful. Oncology experience highly desireable. ...

  19. 3921970 – Process Validation Engineer III

      Responsibilities:                Review Stage 1 Process Design documents, including the Process Description and Parameter Justification Report Write and Review Stage 2 Process Qualification protocols and reports Review the following:   -FMEA reports -Process Risk Mitigation Plans -Process Criticality Assessments -Technology Transfer protocols and reports   Write and Review process validation plans, protocols and reports Assist in preparation and execution of process ...

  20. Manager, Data Analytics

    Current Need McKesson is seeking a  Manager, Data Analytics to work with internal and external customers to understand purchasing requirements, order behavior, contract setup, and pricing management.   Position Description The Manager,  Data Analytics will be lead the development and resolution of critical / urgent initiatives needed to support customer growth and generics expansion in the Retail National Account segment.   The Manager, Data Analytics will also serve as a proactive agent of ...

  21. Director, Strategic Business Development

      Current Need McKesson is currently seeking a Director, Strategic Business Development to oversee all generic sales, customized solutions, and other generic opportunities with the third largest generics purchaser in the retail segment. Position Description This position will be responsible for the development of critical process, accountable for opportunity creation and issue resolution, and will work to ensure critical knowledge disseminated in order to drive profitable market share growth. ...

  22. Manager, Strategic Programs

    Current Need McKesson is seeking a Manager of Strategic Programs to be responsible for executing strategic programs associated with sourcing and virtual sequestering of products for select Generics National Accounts customers. Position Description The Manager of Strategic Programs will help lead the on-going development of key technologies need to support this rapidly growing segment of business to ensure we meet the needs of our customer and drive differential value.  Additionally the Manager of ...

  23. Finance Operations Manager

    Current Need McKesson is seeking a Finance Operations Manager to manage the Generics Customer Rebates operations, accounting and analytics for key customer groups within the RNA and Hospital segments, which totals approximately $400 million annually in rebate payments to 40 big customers. Position Description Manage the administration rebate reports, validations, payments and accruals for accuracy. Manage the contract review process, interpretation of customer agreements and set up of rebates in ...

  24. ETA Scientist

    :: Contact Mary for details at 815-756-1221. Attach resume when responding to this posting :: The ETA Scientist will be responsible for assessing and implementing new, external technologies for the global R&D and ETA function. They will identify new opportunities and work to advance R&D projects and implement them. Qualifications: - BS Degree - 5-10 years of relevant experience - Working knowledge of variety of technologies, development processes, product portfolios, etc. - Experience in open ...