Current jobs related to Sr. Associate, Quality - Novato, California - BioMarin Pharmaceutical Inc.


  • Novato, California, United States TalentBurst Full time

    Quality Assurance Associate **Job Summary** TalentBurst is seeking a Quality Assurance Associate to provide quality oversight of operations. The ideal candidate will have a strong understanding of GMP regulations and industry standards. **Responsibilities** * Review GMP documentation from manufacturing, including logbooks, production batch records, and...


  • Novato, California, United States Randstad Full time

    Job SummaryWe are seeking a highly skilled Quality Assurance Associate to join our team at Randstad. As a Quality Assurance Associate, you will be responsible for providing quality oversight of operations, including review of GMP documentation, scanning and archiving of production batch records, and ensuring manufacturing adherence to company policies and...


  • Novato, California, United States Randstad Full time

    Job Summary:We are seeking a highly skilled Quality Assurance Associate to join our team at Randstad. As a Quality Assurance Associate, you will be responsible for providing quality oversight of operations, including review of GMP documentation, scanning and archiving of production batch records, and ensuring manufacturing adherence to company policies and...


  • Novato, California, United States Randstad Full time

    Job SummaryWe are seeking a highly skilled Quality Assurance Associate to join our team at Randstad. As a key member of our operations team, you will be responsible for ensuring the quality and compliance of our manufacturing processes.Key ResponsibilitiesReview and verify GMP documentation, including logbooks, production batch records, and electronic buffer...


  • Novato, California, United States Compass Consulting Full time

    Compass Consulting: Quality Assurance AssociateWe are seeking a highly skilled Quality Assurance Associate to join our team at Compass Consulting. As a key member of our operations team, you will be responsible for ensuring the quality and compliance of our manufacturing processes.Key Responsibilities:Review and verify GMP documentation, including logbooks,...


  • Novato, California, United States Randstad Full time

    Job Summary:We are seeking a highly skilled Quality Assurance Associate to join our team at Randstad. As a Quality Assurance Associate, you will be responsible for providing quality oversight of operations, including review of GMP documentation, scanning and archiving of production batch records, and ensuring manufacturing adherence to company policies and...


  • Novato, California, United States BioSpace, Inc. Full time

    Job SummaryBioSpace, Inc. is seeking a highly skilled Senior Quality Associate to join our team in the Technical Operations group. As a key member of our quality assurance team, you will be responsible for ensuring the highest standards of quality and compliance in our manufacturing processes.Key Responsibilities:Provide on-the-floor quality assurance...


  • Novato, California, United States Planet Pharma Full time

    Job SummaryWe are seeking a highly detail-oriented Quality Assurance Associate to join our team at Planet Pharma. As a key member of our operations team, you will be responsible for ensuring the quality and compliance of our manufacturing processes.Key ResponsibilitiesReview and verify GMP documentation, including logbooks, production batch records, and...


  • Novato, California, United States Compass Consulting Full time

    At Compass Consulting, we are dedicated to delivering exceptional services to our clients in the pharmaceutical industry. As a Quality Assurance Associate, you will play a critical role in ensuring the highest standards of quality and compliance in our operations.Key Responsibilities:Provide quality oversight of one or more portions of operations, including...


  • Novato, California, United States Planet Pharma Full time

    Job Summary:Planet Pharma is seeking a highly detail-oriented and organized Quality Assurance Associate to provide quality oversight of operations, ensuring adherence to company policies, regulatory licenses, industry standards, and Good Manufacturing Practices (GMP) regulations.Key Responsibilities:Review and verify GMP documentation, including logbooks,...


  • Novato, California, United States Harvest Technical Services Full time

    Job SummaryWe are seeking a highly skilled Quality Assurance Associate to join our team at Harvest Technical Services. As a key member of our operations team, you will be responsible for providing quality oversight of various aspects of our manufacturing process.Key ResponsibilitiesReview and verify GMP documentation, including logbooks, production batch...


  • Novato, California, United States Talent Software Services Full time

    Job Summary:Talent Software Services is seeking a Quality Assurance Associate to support our operations in Novato, CA.**Key Responsibilities:*** Review and verify GMP documentation from manufacturing, including logbooks, production batch records, and electronic buffer & media batch records.* Ensure manufacturing adherence to company policies, regulatory...


  • Novato, California, United States Randstad Full time

    Job SummaryWe are seeking a highly skilled Quality Assurance Associate to join our team at Randstad. As a key member of our operations team, you will be responsible for ensuring the quality and compliance of our manufacturing processes.Key ResponsibilitiesReview and approve GMP documentation, including logbooks, production batch records, and electronic...


  • Novato, California, United States inSync Staffing Full time

    Job SummaryWe are seeking a highly detail-oriented QA Operations Associate to provide quality oversight of operations, ensuring adherence to company policies, regulatory licenses, industry standards, and GMP regulations.Key ResponsibilitiesReview GMP documentation from manufacturing, including logbooks, production batch records, and electronic buffer & media...


  • Novato, California, United States Randstad Full time

    Job SummaryWe are seeking a highly skilled Quality Assurance Associate to join our team at Randstad. As a key member of our operations team, you will be responsible for ensuring the quality and compliance of our manufacturing processes.Key ResponsibilitiesReview and approve GMP documentation, including logbooks, production batch records, and electronic...


  • Novato, California, United States Randstad Full time

    Job SummaryWe are seeking a highly skilled Quality Assurance Associate to join our team at Randstad. As a key member of our operations team, you will be responsible for ensuring the quality and compliance of our manufacturing processes.Key ResponsibilitiesReview and verify GMP documentation, including logbooks, production batch records, and electronic buffer...


  • Novato, California, United States BioMarin Full time

    **About the Role**BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. Our team of engineers, technicians, scientists, and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance...


  • Novato, California, United States Talent Software Services Full time

    Job SummaryTalent Software Services is seeking a Quality Assurance Operations Associate for a contract position. The opportunity will be four months with a strong chance for a long-term extension.Key ResponsibilitiesReview of Good Manufacturing Practice (GMP) documentation from manufacturing, including logbooks, production batch records, and electronic...


  • Novato, California, United States Harvest Technical Services Full time

    Job SummaryHarvest Technical Services is seeking a highly skilled Operations Quality Assurance Associate to provide quality oversight of various operations, ensuring adherence to company policies, regulatory licenses, industry standards, and Good Manufacturing Practices (GMP) regulations.Key ResponsibilitiesReview and verify GMP documentation, including...


  • Novato, California, United States BioSpace, Inc. Full time

    Job DetailsAbout UsBioSpace, Inc.'s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. Our team of engineers, technicians, scientists, and support staff build and maintain our cutting-edge manufacturing processes and sites, provide quality assurance...

Sr. Associate, Quality

4 months ago


Novato, California, United States BioMarin Pharmaceutical Inc. Full time
Who We Are


BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market.

These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.

Senior Associate, Quality – On-Site Grave and

Weekend Shift Responsibilities:

  • Provide on the floor QA oversight and support to manufacturing operations
  • Review executed batch records and associated document to ensure compliance with approved procedures and cGMP expectations
  • Respond to quality related incidents or non conformances on the floor and secure necessary documentation for real time investigations
  • Represent QA in support of deviations including active participation in Root Cause Analysis (RCA)
  • Provide cGMP and compliance guidance to Manufacturing and Manufacturing Sciences and Technology (MSAT) personnel
  • Provide QA support including write, review, and approve documents in Quality Management Systems in accordance with BioMarin policies
  • Perform area walkthroughs
  • Perform other duties and projects as assigned by management Experience and

Other Qualifications:

  • BS/BA in a scientific discipline or related field and 6 8 years experience in a biologics manufacturing environment
  • Prior batch record review experience is required
  • Prior experience in investigation, change control, other Quality Management Systems (QMS)
  • Working knowledge of cGMPs
  • Excellent written and verbal communication and interpersonal skills
  • Must display strong analytical and problem solving skills
  • Manufacturing and MSAT experience preferred Please note that while this role primarily involves night and weekend shift hours, there may be occasions where the need for flexibility is required, as shift hours can vary depending on operational demands

Shift Details:
Alternate Wed, Thurs-Sat No international travelling required.
Equal Opportunity Employer/Veterans/Disabled

An Equal Opportunity Employer.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.