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Biotech, R&D, & science in San Francisco Bay Area

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  1. Technical Writer / Medical Writer

    A highly reputable and distinguished pharmaceutical corporation is currently looking for a Technical Writer / Medical Writer to work in Emeryville, CA. Provide technical writing and administrative services in support of instrument and software operator manuals, product inserts, labels, specifications and training materials: Edit and/or write software, instrument, and assay instructions for use using FrameMaker, within established formats and guidelines. Design and edit product labels using ...

  2. Global Study Associate

    Hello,   My name is Sarah and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Global Study Associate for a prominent client of ours.  This position is located in South San Francisco, CA. Details for the positions are as follows:   Job Description The CTA / GSA manages the Automated Clinical Request System (ACRS) Enters patient and site information, keeps up to date the names and addresses for investigators Keeps Trial Master File (TMF) up to date ...

  3. QA Inspector

      Candidates cannot begin an assignment without successful completion of drug and background screenings. 3 Month Contract Assignment $18.00 Hourly High school diploma, 2 years of experience in GMP or ISO environment. 2 years experience in a quality function. Responsibilities: Supports Reagent Vialing and Packaging, Planning, QC, Formulation, and Custom Reagent Depts. Reports to Quality Assurance Manager. Performs final inspection, line clearance, includes verifying product labeling, reviewing ...

  4. EHS Engineer

      EH&S Engineer (Contract 6 months) Castro Valley, CA area Description   Essential Duties/Responsibilities: •    Work with department supervisor/manager to investigate industrial accidents, injuries, or near misses to determine causes and preventive measures. •    Track corrective action proposed by department supervisor/manager in response to industrial accidents. •    Develop, conduct, coordinate, and track safety training. •    Review and update safety procedures. •    Compile, analyze, and ...

  5. Production Engineering Mechanic

      Mechanic, Production Engineering - 2nd Shift  Engineering | Castro Valley, CA Essential Duties & Responsibilities include the following:  Other duties may be assigned. Observes mechanical devices in operation and listens to their sounds to locate causes of trouble. Dismantles devices to gain access to and remove defective parts. Examines form and texture of parts to detect imperfections. Inspects used parts to determine changes in dimensional requirements Adjusts functional parts of devices and ...

  6. Maintenance Mechanic (Utility)

     Description (2nd Shift)    Essential Duties & Responsibilities include the following:  Other duties may be assigned. •Observes mechanical devices in operation and listens to their sounds to locate causes of trouble. •Patch, repair and paint building walls, ceilings and flooring. •Repair building systems such as doors, windows, HVAC, plumbing etc. •Repairs electrical equipment. •Replaces and repairs light bulbs or ballasts in all assigned facilities •Performs plumbing repairs, as necessary •Performs ...

  7. Machinist

      Description (1st Shift)   Essential Duties & Responsibilities includes, but is not limited to the following: Other duties may be assigned. •Maintain proper documentation for inspections, cleanings, log books, inventory lists, Out of Service, PMs, Corrective Work Orders, etc. •Inspects and cleans tooling which includes, but is not limited to tablet presses parts (punches and dies, etc.), •Inspect, repair or replace encapsulation change parts (dosators, pistons, beaks, etc.), imprinter parts ...

  8. Maintenance Mechanic Stock Room

    Description (2nd Shift) Essential Duties & Responsibilities include the following: Other duties may be assigned. • Observes mechanical devices in operation and listens to their sounds to locate causes of trouble. • Dismantles devices to gain access to and remove defective parts. • Examines form and texture of parts to detect imperfections. • Inspects used parts to determine changes in dimensional requirements • Adjusts functional parts of devices and control instruments. • Monitoring of Building ...

  9. 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 ...

  10. 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 ...

  11. Method Validation Scientist / 105276

     CONTRACT / 7-9 MONTHS ... COULD BE EXTENDED Responsible for developing, optimizing, and validating release, in-process, raw materials and cleaning methods in support of Grifols Diagnostic Solutions immunodiagnostic intermediates. This role will interact with Technology Development, Manufacturing, Research & Development, Quality Control and Quality Assurance staff to ensure that method validation and transfer studies are appropriate for the methods’ intended use(s) and comply with applicable ...

  12. Scientist, Translational Development

    Our client, a large reputable pharmaceutical company, is currently seeking a Scientist, Translational Development. Under moderate supervision in a fast-moving team-based environment, the Contractor will provide biomarker specimen and clinical trial support across multiple studies in oncology and inflammation/immunology, execute on biospecimen operations logistics, track biospecimens using a laboratory inventory management system, and provide biospecimen processing training. As part of the ...

  13. Lab Technician

    ~~ JOB SUMMARY/PURPOSE    Provide technical support for projects involving mineral product characterization and testing of filtration characteristics of those products.  Activities will contribute to the ongoing efforts toward product innovation and customer support.   KEY TASKS AND RESPONSIBILITIES   1.Conduct laboratory testing in an accurate and timely manner on a variety of analytical instruments including particle distribution (by sedimentation, laser diffraction, and/or sieve analysis), BET ...

  14. SAS Programmer / Clinical / WORK FROM HOME / 8+ yrs exp.

    SAS Programmer / Clinical / WORK FROM HOME / 8+ yrs. experience The Gerard Group has been asked to locate, qualify and present a SAS Programmer for a full time TELECOMMUTE opportunity. Â Key Accountabilities/Core Job Responsibilities: The ideal candidate will provide statistical programming support and validation of analysis datasets, create statistical tables, graphs and listings for clinical trial data. CDISC experience (i.​e.​ SDTM & ADaM) required. Â Qualifications/Experience/Education: ...

  15. Associate Director Statistical  Programming – SAS/oncology – CDISC  SF

    ~~Associate Director Statistical programming – oncology – CDISC - Full time position. Our San Francisco Peninsula Client has asked us to locate, qualify and present Associate Director Statistical Programming ~~ Accountable for statistical programming activities performed by a team of statistical programmers, ensuring timelines are met and best practices implemented. • Create and manage project and study phase sub-directories ensuring consistency in processes and database structures across studies ...

  16. 3986332 – Method Validation Scientist

      Responsibilities: Responsible for developing, optimizing, and validating release, in-process, raw materials and cleaning methods in support of immunodiagnostic intermediates.  This role will interact with Technology Development, Manufacturing, Research & Development, Quality Control and Quality Assurance staff to ensure that method validation and transfer studies are appropriate for the methods' intended use(s) and comply with applicable regulatory and company validation requirements   ...

  17. 3985834 – Scientist – QA

    Responsibilities: Serve as Quality Partner for local QARs, EQNCs, CAPAs and Trackwise entry assuring completion in a timely and compliant manner Review and approval of Clinical Validation Plans, Clinical Protocols and Clinical Reports Review and approval of local IQOQ protocols Review and approval of Design History Files including Design Protocols, Reports and Plans Provide assistance during audits of the Quality System and Clinical Operations Requirements: Bachelor's degree in ...

  18. Applications Lab Technician

    Job Title:       Applications Lab Technician Department:  Marketing                                                                                                                                  Status:         Nonexempt; eligible for overtime pay Hours:          Typically Monday through Friday; core hours may vary Travel:           Less than 10% Reports to:    Product Manager Supervises Others:       No   SUMMARY Under general supervision, support the Marketing Department and R&D Lab with ...

  19. Senior Electrical Engineer

    We are looking for a hands-on Senior Electrical Engineer to support the organization in support of the Company’s goals and objectives. The ideal candidate would have had previous medical device experience. This position will report directly to the Senior Director of R&D. The Senior Electrical Engineer will be responsible for developing electrical systems for Procept’s products. Development includes feasibility, requirements definition, design, design verification, test system development, ...

  20. Director, Quality Assurance and Regulatory Affairs

    We are a small, private, medical device start-up company launching our first product. We are looking for a hands-on Quality Assurance and Regulatory Affairs Director who will responsible for all aspects of the quality and regulatory activities at the company. This person will be responsible for developing strategies for worldwide approval to introduce new and/or modified products to market. As the Management Representative, the Director has overall responsibility for the development, implementation ...

  21. Senior Quality Engineer

      We are looking for a hands-on Senior Quality Engineer to support the Quality Organization in implementing, facilitating, and maintaining the Corporate Quality System for all clinical/commercial products and devices in support of the Company’s goals and objectives. The ideal candidate would have had previous medical device experience. This position will report directly to the Manager QA & RC. The main purpose of this role ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties ...

  22. Medical Advisor (Nationwide)

    Our client is seeking a Medical Advisor II that will provide medical and scientific support to both internal team members and external healthcare decision makers and respond to information inquiries. The Medical Advisor will provide scientific support to the commercial activities, research, marketing, and report safety issues within the region consistent with legal and regulatory requirements.   Responsibilities: •Develop and manage relationship with Thought Leaders through scientific exchange ...

  23. Associate Research Scientist / 105265

     CONTRACT / 4-6 MONTHS...GREAT OPPORTUNITY Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors. Exercises judgment within defined procedures and practices to determine appropriate action. Under direct supervision, executes on assigned tasks (routine testing) following appropriate laboratory/technical procedures. Makes detailed observations and analyzes data to provide some interpretation of results. Assists with the investigation, ...

  24. Senior Clinical Research Associate(office based) - Contract

    Our client, a growing biotechnology company in the San Francisco, CA area is looking for a contract  Senior CRA to work office based in their San Rafael offices(this is not a home based opportunity). The Senior CRA will provide oversight work (vendor management, site management, data review, trip report reviews, etc.).  PKU experience required. Metabolic experience a plus!