Sr Manager of QA
- Contract
- Good Manufacturing Practice (GMP)
- United States
Sr Manager of QA - Contract - Cranbury, NJ
黑料视频 is seeking a Sr Manager of QA to oversee quality assurance activities at a GMP viral vector drug substance manufacturing and testing facility.
Primary Responsibilities:
The successful candidate will ensure compliance with quality standards and regulatory requirements, while enhancing quality systems and processes such as validation, material control, risk management, and training.
Skills & Requirements:
- BS degree in biological sciences or related field of study. Advance degree is a plus
- Minimum 8 years of relevant experience in biological sciences or biotechnology within quality assurance, quality control, biomanufacturing, clinical and/or regulatory operations.
- Minimum 6 years of experience with Masters degree in biological sciences or biotechnology
- Familiarity with cell and gene therapy regulations.
- Knowledge of cGMPs and international regulations.
- Ability to interpret and apply regulatory compliance requirements.
- Strong communication skills.
- Ability to work in a cross-functional team in a dynamic environment.
The Sr Manager of QA's responsibilities will be:
- Support the transition from phase-appropriate to commercial GMP activities.
- Review and approve equipment, utility, and facility qualification/validation protocols.
- Conduct product release activities, including batch record reviews.
- Assess and approve analytical documents, including validation protocols and testing data.
- Evaluate change controls for risks and impacts.
- Identify and escalate critical compliance and quality assurance issues.
- Review data for internal reports and regulatory submissions.
- Collaborate with experts to improve processes and procedures.
- Approve SOPs, specifications, and controlled documents.
- Track and trend deviations and corrective actions.
- Ensure timely closure of audit observations and corrective actions.
- Support risk assessments and mitigation activities.
- Coordinate quality assurance activities during technology transfer projects.
If you are having difficulty in applying or if you have any questions, please contact Anderson Maldonado at a.maldonado@proclinical.com
黑料视频 is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
黑料视频 Staffing is an equal opportunity employer.
INDCQA
Related jobs
US$30.00 - US$41.00 per hour
New Haven, USA
黑料视频 is working alongside a pharmaceutical company seeking a QA Documentation Manager to join their growing team.
Highly Competitive
Göttingen, Germany
黑料视频 sucht für ein Pharmaunternehmen einen Laborant (m/w/d) QC.
Highly Competitive
Philadelphia, USA
黑料视频 is partnered with a pharmaceutical company seeking a QA Raw Materials Supervisor for a role in Philadelphia, PA.
Highly Competitive
Philadelphia, USA
黑料视频 is working alongside a pharmaceutical company seeking a QA Release Supervisor, Cell Therapy to join their team!
Highly Competitive
Philadelphia, USA
黑料视频 is seeking a highly motivated QA Specialist II to join the Quality Operations team for a night shift role.
Highly Competitive
Cambridge, England
黑料视频 is currently working alongside a consultancy company to recruit for a Head of Quality & Operations. This is a permanent position based in Cambridge, United Kingdom.