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document control in San Francisco Bay Area

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  1. Information Security Engineer at Rally Health

    Bachelor’s degree in management information systems, computer science, or related discipline is required....

  2. Big Data Engineer/ Senior Data Engineer at Ancestry

    Experience with R and/or MatLab. Big Data team is looking for an experienced Data Engineer who has a passion to build data products and data systems....

  3. Licensed Clinical Social Worker (Psych Emergency Dept) at Marin General Hospital

    D. Documents all collateral contracts. D. Maintains positive working relationships with community agencies. Oversees physician’s need for timely submission of...

  4. Licensed Clinical Social Worker or Clinical Social Worker (MSW) (Sign On Bonus) at Marin General Hospital

    D. Documents all collateral contracts. D. Maintains positive working relationships with community agencies. Oversees physician’s need for timely submission of...

  5. Market Planning Manager – Pharma/Biotech W2 ONLY at Consultant Specialists, Inc. (CSI)

    BS/BA with business, finance or science concentration preferred. 4597268 Market Planning Manager – Pharma/Biotech W2 ONLY 8 Month Contract....

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    1. Associate Scientist, Analytical Chemistry

      Purpose: This role supports Pearl MDI product development from product definition stages to product approval and launch by devising, leading, and conducting analytical experiments.Duties and Responsibilities: Design experiments and conduct analytical experimental work related to advancing Pearl product quality and performance.Lead projects within areas of expertise.Identify aberrant data and ...

    1. Senior Writer and Content Strategist at Veeva Systems

      The cloud and life sciences. We build innovative SaaS solutions that include CRM, content management, and customer master data management for life sciences...

    1. Senior Process Equipment Engineer

      Purpose: A member of the Process Engineering Team engaged in specifying, designing, fabricating, purchasing, and managing pilot to commercial scale process equipment.Duties and Responsibilities: The principal objective of this position is to ensure manufacturing equipment is designed, built, and operating per internal and regulatory requirements. Some Equipment is custom designed by Pearl and ...

    1. Information Security Analyst at Gymboree

      Identify mitigating controls. (security controls / assessments / compliance. Create and maintain security-related documents....

    1. Sr. Scientist / Principal Scientist Synthetic Chem Process Dev 1491

      Description:Reporting to the Senior Director of Chemical Development, the successful incumbent will work on all process chemistry aspects of new small molecule pharmaceuticalsAssisting in oversight of CMO activities related to technology transfer, development, optimization, scale-up and manufacture of drug substance and related materialsReviewing, verifying and approving process documentation ...

    1. Sr. Cisco Network Security Engineer at Solutionary, Inc.

      Document policies and operating procedures. Coordinate with client change control process, maintenance windows....

    1. Principal Engineer, Semiconductor Electro-Mechanical, & RF

       JOB SUMMARY Principal EngineerResponsible to lead teams that include electrical, mechanical and software engineering members to design, integrate, test and troubleshoot complex semiconductor equipment systems and sub systems through a new product life cycle. Troubleshoot RF electrical and electromechanical issues and implement corrective action for existing products.KEY RESPONSIBILITIES• ...

    1. Network Security Information Assurance Engineer at Vectrus

      OR Associate degree in Computer Science, Computer Science Technology,. Bachelor of Science degree in electrical/electronics engineering, computer/software...

    1. Contract -  Goverance Analyst

      Harvest Technical Services is seeking a Contracts - Governance Analyst for our Greater San Francisco Bay Area Biotech clientDuties/Responsibilities:Provide oversight of supplier reporting to ensure timely, accurate reports on: operations, issues, and stakeholder satisfaction.Ensure appropriate internal reviews, decisions are made per process requirements and provide reporting to executives ...

    1. Diagnostic Medical Sonographer / St. Vincent's Southside / PRN Rotating at St. Vincent's Southside

      Implements safety standards and performs appropriate quality control procedures. Provides prompt submission of all images and documents to PACS....

    1. Scientist II

      Scientist II, Sequencing Development The ScientistII will be a member of the VirologyAssay Development team working ontests for use on next-generation sequencing systems. The successful candidate will develop and implement strategies for infectious disease related NGSapplications including nucleic acid extraction, amplification, library preparation, sequencing, and data analysis. Key Roles ...

    1. Diagnostic Medical Sonographer / SVM-St Vincent's Riverside / PRN Rotating at SVM-St Vincent's Riverside

      Implements safety standards and performs appropriate quality control procedures. Provides prompt submission of all images and documents to PACS....

    1. Sr/Principal Project Manager

      Our client is seeking an experienced Project Manager to lead the development of core products. This is a critical role and applicants should have a track record of success in delivering new products to market.As a Project Manager in the endoscopy division, you will lead cross-functional teams to create and improve medical devices used by surgeons. You will develop and deliver products which ...

    1. Diagnostic Medical Sonographer / St Lukes Hospital / FT Evenings at St Lukes Hospital

      Implements safety standards and performs appropriate quality control procedures. Provides prompt submission of all images and documents to PACS....

    1. Director, Quality

      About the Role:As Director of Quality, you will lead and manage development and implementation of an FDA QSR and ISO 13485 compliant quality management system while supporting existing quality and regulatory activities of the CLIA-certified, CAP-accredited laboratory. You’ll partner with functional leaders and be an advocate and champion of quality programs. As the company grows and ...

    1. Information Security & Compliance Analyst at FireEye

      Performing control assessment based on security standards and platform critical controls. Bachelor’s degree in Computer Science or related field....

    1. Sr. Manager, Quality Device Engineer 1306

      Description:Responsible for leading and managing the design control efforts for combination products and/or devices in accordance with FDA and other global regulations (21CFR4, 210/211, 820, IS0 13485, ICH Q9, and Q10).Will lead and/or support all quality engineering, qualification and validation activities of the product life cycle, from development through commercialization.Establish and ...

    1. Information Security Engineer at HEAT Software

      Bachelor’s degree in management information systems, computer science, or related discipline is required....

    1. QA Manager

      Location: East Bay, CAThe Quality Manager I will be responsible for developing and maintaining ISO 13485 and FDA QSR compliant design control processes for the Digital Biology Center (DBC) . Our Client is a leader in the development of innovative droplet digital PCR systems representing a new era in reliability and affordability across a range of applications for life science researchers and ...

    1. Information Security Analyst (Incident Response) at Finezi Inc

      Recommends implementation of counter-measures or mitigating controls. Document investigation results, ensuring relevant details are passed to senior analysts...

    1. QA  Manager

      Location: East Bay, CAThe Quality Manager I will be responsible for developing and maintaining ISO 13485 and FDA QSR compliant design control processes for the Digital Biology Center (DBC) . Our Client is a leader in the development of innovative droplet digital PCR systems representing a new era in reliability and affordability across a range of applications for life science researchers and ...

    2. QA Manager

      Location: East Bay, CAThe Quality Manager I will be responsible for developing and maintaining ISO 13485 and FDA QSR compliant design control processes for the Digital Biology Center (DBC) . Our Client is a leader in the development of innovative droplet digital PCR systems representing a new era in reliability and affordability across a range of applications for life science researchers and ...

    3. Senior Process Equipment Engineer

      Purpose: A member of the Process Engineering Team engaged in specifying, designing, fabricating, purchasing, and managing pilot to commercial scale process equipment.Duties and Responsibilities: The principal objective of this position is to ensure manufacturing equipment is designed, built, and operating per internal and regulatory requirements. Some Equipment is custom designed by Pearl and ...

    4. Senior Manager, Quality Assurance Systems

      Summary: The Senior Manager, Quality Assurance Systems will report to the Vice President, Quality Assurance. This individual will support quality and regulatory compliance with GMP, GCP and GLP requirements and will help assure the quality aspects of drug substance/drug product manufacturing at contract service providers (CSP). The incumbent will lead the Versartis quality team’s activities ...

    5. Validation Engineer – Cleaning

      Azzur Group of CA is seeking Validation Engineers with Cleaning experience to join our growing Northern California team. The Validation Engineer will be knowledgeable of all aspects of equipment cleaning validation and will work closely with QA, engineering, maintenance and production personnel to ensure all activities are completed on schedule. Essential Duties and Responsibilities· Prepare ...

    6. Regulatory Affairs Associate I

      Education:·        A four-year degree in life sciences (science degree preferred) Duties:·        Develop timelines for Regulatory Labeling activities (deliverables for submission) and update Global Decision Tracking (labeling tracker)·        QC text for labeling of pharmaceutical products as required by FDA (21 CFR 201), EU guidance and other international labeling regulations.·        ...

    7. Biopharma Regulatory Affairs Opportunities, all levels! N+South Bay

      Several exciting Regulatory Affairs opportunities are now accepting and screening candidates for three levels of opportunities - entry, junior, and senior. Those with previous experience in document control, clinical submissions, and regulatory affairs are encouraged to apply. Senior level opportunity is targeting experience in CMC. Duties:Develop timelines for Regulatory Labeling activities ...

    8. Director - Clinical Development - Skin & Joint Inflammation

      Seeking MD with Clinical Development and medical leadership experience who can lead clinical trials for new drugs aimed at treating autoimmune disorders causing inflammation of the skin, joints, and connective tissues. Shall: *** Manage all efforts involved in the design and execution of multiple ongoing clinical studies in Phase I through III. *** Write clinical sections of regulatory ...

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    9. Quality Control Scientist 1475

      Description:Modify existing methods and/or develop and optimize new QC methods to support routine lot release of reagents and kits used in the CLIA laboratory.The Scientist will work hands on to carry out experiments and studies with minimal guidance to support bio-chemical verification and validationDesign and development of reagent Quality Control (QC) Tests and associated bio-chemical ...

    10. Document Controller

      A Bay Area Pharmaceutical company is looking for a Document Controller/Standards Specialist to join their team in supporting rare diseases.Duties:The position is responsible for actively supporting the quality and management of Controlled Documents (including Standard Operating Procedures, Work Instructions, Forms, Templates) for the Development Sciences (DevSci) organization.  This position ...

      1. Bio/Pharma Freelance Writer at Bulletproof Documentation, Inc.

        SOPs, Biotech, Pharmaceutical, Documentation:. Experience working with large volumes of documents. Duties/Responsibilities:....

      2. Research Associate I at Comparative Biosciences, Inc

        0-5 years’ experience working in a pharmaceutical, biotech or Contract Research Organization (CRO), preferably in pre-clinical development....

      3. Cyber Information Security Director at Vectrus

        Documents and reports incidents from initial. Security controls through recommendations of new policies, procedures and....

      4. Information Assurance (IA) Specialist (On Call) at Northrop Grumman

        Coordinate with other team members to prepare and submit interface control documents. Possesses a bachelor’s degree in IA, IT or computer science....

      5. Senior Information Technology Analyst (S... at County of San Mateo

        Quality control methods used to assure data accuracy and integrity. Examples include a requirements document, logic flow chart, data flow diagram, and entity...