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biotechnology in San Francisco Bay Area

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  1. Entry level Inside Sales/Customer Service

    TOP Group is one of the biggest bilingual recruiting companies in the nation. We have businesses with international firms in San Francisco, Los Angeles, Portland, Seattle, throughout the West Coast region, across the United States, Mexico, Canada, and Japan. We have been successfully serving major corporations, Fortune 500 companies, and professional individuals seeking employment for over 20 years. We are currently hiring for a Full Time Customer Service Rep/Inside Sales Rep for a Japanese ...

  2. Senior Clinical Research Associate – Full Time Position

      Description   Responsible for implementing set-up, execution, oversight and reporting of clinical studies while ensuring that the conduct of the trial is in compliance with the protocol, ICH/GCP, and applicable regulatory requirements.   Key Accountabilities/Core Job Responsibilities: Lead multifunctional team through clinical studies activities that meet ICH/GCP and SOP requirements Develop clinical trial protocol synopsis, protocols, amendments and informed consent documents Develop ...

  3. 3914925 – Glassware Technician III

      Requirements: Must have strong written and verbal skills. Must be able to work in a team-oriented environment. Must be creative, highly organized, self-motivated, perceptive, and innovative. Must have strong analytical and decision making skills. Able to make decisions with limited supervision.   Technical skills requirements   Must have experience in GMP manufacturing. Must have experience in FDA and ISO regulated environments. Must have adequate knowledge of reagent preparation ...

  4. Protein Purification Associate - 104892

    Laboratory Associate I, Purification Sciences – 6 month contract Perform scaled down purification studies to support the development of new processes, or to improve the existing manufacturing processes, in addition to providing support for QC or Manufacturing deviations investigations. Working under moderate to high degree of supervision from Lab Manager and/or senior Associates II: Executing scientific protocols in a team setting using scaled down column chromatography operations and ultra/dia ...

  5. Validation Engineer - CQV Specialist - Project Manager

    Validation Engineer - CQV Specialist - Project Manager "The scope of work would comprise of commissioning & qualification of facility, utility, equipment and computerized systems, as well as cleaning development and cleaning validation for process equipment" Experience: Facility qualification / validation and must understand commissioning and adhere to validation and quality guidelines. Familiar with support systems, bioprocess unit operations, process utilities; knowledge of good manufacturing ...

  6. Validation Specialist ( Cleaning / CIP )

    Validation Specialist (Cleaning / CIP) "Need a person with experience in CIP and cleaning validation" Experience: Facility qualification / validation and must understand commissioning and adhere to validation and quality guidelines. Familiar with support systems, bioprocess unit operations, process utilities; knowledge of good manufacturing practices and good documentation practices is required as well as the ability to work independently on projects and/or manage their assigned projects. ...

  7. Validation Engineer - CQV Specialist

    Validation Engineer - CQV Specialist "2-8 year experience range. Basic CQV- writing and executing protocols. Engineering degree preferred" Experience: Facility qualification / validation and must understand commissioning and adhere to validation and quality guidelines. Familiar with support systems, bioprocess unit operations, process utilities; knowledge of good manufacturing practices and good documentation practices is required as well as the ability to work independently on projects and/or ...

  8. Validation Enigneer - CQV Specialist

    Validation Engineer - CQV Specialist ( Fortune 100 Company ) "Experience with clean utilities (Water for Injection, Purified Water, Clean steam, clean compressed air) and Biopharm processing equipment (bioreactors, fermentors, TFF skids, media and buffer prep, centrifuges, purification skids, chromatography) would be helpful. They also need to know how to use a Kaye validator for temperature mapping" Experience: Facility qualification / validation and must understand commissioning and adhere to ...

  9. Validation Specialist - Engineer

    Validation Specialist - Engineer "Validation (CQV) experience in writing and executing documents with experience in purification (chromatography), filtration, overall downstream processing for biotech equipment" Knowledge: Facility qualification / validation and must understand commissioning and adhere to validation and quality guidelines. Familiar with support systems, bioprocess unit operations, process utilities; knowledge of good manufacturing practices and good documentation practices is ...

  10. Global QA Compliance Associate Director Medical Devices

      Position: Major Tasks Provide expert leadership in medical device regulations in an individual contributor role including: the ability to identify issues of significance, communicate complex issues to site leadership, provide multiple alternatives to the solution of complex problems and the ability to provide guidance in their implementation. Leads relevant medical device project planning and review meetings; communicating to senior leadership regarding program status and supporting final ...

  11. 3872278 - Laboratory Associate I, Purification Sciences

    Responsibilities:   Perform scaled down purification studies to support the development of new processes or to improve the existing manufacturing processes in addition to providing support for QC or Manufacturing deviations investigations. Working under moderate to high degree of supervision from Lab Manager and/or senior Associates II. Executing scientific protocols in a team setting using scaled down column chromatography operations and ultra/dia-filtration. Ensuring their own experimental ...

  12. CMC Writer I (Technical Writing)

    We currently have a need in South San Francisco,CA for a CMC Writer I. This assignment is slated to last 12 months. Please email me if you're interested. I have included job description below.             The candidate will assist process development scientists with technical writing of general scientific reports and validation protocols/reports. The candidate should have a basic understanding of biotechnology purification and experience with writing technical manuscripts. General supervision ...

  13. Global Market Planning Manager, Immunology and Ophthalmology

    Global Product Strategy, the department to which this position belongs to, provides strategic business direction from research through to development, commercialization and medical excellence, collaborating with functions and affiliates to shape the future of medicine. The Strategic Insights & Analysis Team provides high quality insights on the brand(s) and the market environment for the relevant disease area based on market research, publicly available brand and market information, and non-publicly ...

  14. Manager, Regulatory Affairs Globsl Labeling

    Global Pharmaceutical company with US Headquarters in California is looking to hire a new Manager, CMC for Biologicsbase salary starts at 100k (and goes higher - midpoint is ideal at 115, all is DOE), plus, bonus, stock, 401k, full medicala nd other LTIsRelocation available Looking for a qualified Manager (Clinical), Regulatory Affairs to manage the clin-nonclin liaison aspects of global regulatory affairs activities in support of product development. Both early and late-stage development projects ...

  15. Manager, Regulatory CMC Biologics

    Global Pharmaceutical company with US Headquarters in California is looking to hire a new Manager, CMC for Biologicsbase salary starts at 100k (and goes higher - midpoint is ideal at 115, all is DOE), plus, bonus, stock, 401k, full medicala nd other LTIsRelocation availableMUST have recent Biologics experienceThe Manager, Regulatory Affairs, is responsible for managing the CMC aspects of domestic and international regulatory affairs for commercial and clinical projects. The candidate will be ...

  16. Director, Business Development, Oncology Drug Development

    My client is expanding their sales force, and they look to hire several additional directors to better service their new and existing clients. The ideal candidate will be responsible for selling services to pharmaceutical and biotechnology clients, and this person will take on the following tasks: Grow and expand the business in the territory, as well as target, prioritize and sell the platform technology Target existing and potential biotech and pharma clients by demonstrating the value and ...

  17. Executive Assistant to Global Biotech Firm

    Compensation for this position is: $80K-$85K plus overtime. Preeminent Biotechnology Firm has an immediate need for an Executive Assistant. This is an amazing opportunity for a bright, personable professional to take charge of a role that contributes to critical aspects of business development and partner with executives who have played a significant role in the firm’s enduring success.   In this role, you will utilize your exceptional organizational skills to provide high level support to the ...

  18. Sr. Clinical Research Associate

    Sr. Clinical Research Associate, Full Time Opportunity - San Francisco Bay Area Relocation assistance may be provided Therapeutic areas:  Oncology, Infectious Disease, Dermatology, CNS or Ophthalmology Responsible for implementing set-up, execution, oversight and reporting of clinical studies while ensuring that the conduct of the trial is in compliance with the protocol, ICH/GCP, and applicable regulatory requirements. Key Accountabilities/Core Job Responsibilities: Lead multifunctional team ...

  19. 3899871 – Associate Scientist I

    B.Sc./M.Sc. in Chemistry/Biochemistry or related discipline 1 to 5+ years of experience in either an Analytical Development or QC Testing environment in the biotechnology or diagnostics industry Prior experience working on Analytical testing of recombinant proteins.    Working under moderate to high degree of supervision on Analytical testing using up to 2 different methods Experience maintaining laboratory scale Analytical equipment Good verbal communication skills     Potential for ...

  20. 3900028 – Associate Scientist III

      Responsibilities:   To perform routine laboratory-based Analytical testing for product release. Ensure the Analytical laboratory equipment, reagents and chemicals are stocked and ready to perform testing according to the Analytical laboratory schedule (80%). Independently perform studies with complex scope with some supervision from the Lab Manager to support purification process characterization, process improvement or investigation of purification process-related deviations using ...

  21. Associate Director, Clinical Data Management

    Key Responsibilities: Oversees Clinical Data Management processes, ensuring timelines and contracts are adhered to and quality standards are met.  Maintains system validation documentation and other regulatory documentation. Manages, monitors and reports on progress of Data Management projects. Responsible for resources planning and tasks assignment of direct reports.  Supports department infrastructure.  Supports department head by successfully completing ad hoc projects to improve departmental ...

  22. Controller -Biotech-$225k base

    Corporate Controller / CFO for Biotech - South SF area. Base $225k ++ This is an exceptional opportunity to lead the finance and accounting function of a successful, small biotechnology company. The Controller will be responsible for financial reporting and accounting, daily and monthly reports and month-to-month and budget to actual variance analyses and will manage all finance and accounting staff. We are looking for an individual who works well in a team environment. This position requires the ...

  23. Clinical Research Associate - Immune Design - San Francisco

    Clinical Research Associate - San Francisco Office   Immune Design Immune Design is leveraging two powerful, versatile discovery platforms of innovative technologies that work in partnership to develop product candidates that activate, guide, and strengthen patient-specific immune responses to potentially fight cancer and other chronic diseases.  The Company was founded in 2008 with cutting edge molecular tools to shape the immune response by selectively activating and targeting dendritic cells.  ...

  24. MECHANICAL ENGINEER

    JOB TITLE: Mechanical Engineer DEPARTMENT: Product Development LOCATION: Los Gatos, CALOA: 6 mo CTHOVERVIEW: This is an exciting opportunity for a Mechanical Engineer to join a fast growing biotechnology company. This position will work in the R&D department in the development on new Biotech and Medical products. The main focus of this position is the design and development of new products from conceptualization to transfer to manufacturing. This company has a fast paced environment with ...