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Quality Assurance Specialist - Contract - Cambridge, MA

À±½·ÊÓƵ is working alongside a pharmaceutical company seeking a Quality Assurance Specialist to join their team.

Primary Responsibilities:

The successful candidate will play a pivotal role in managing activities within a GMP-regulated environment, ensuring adherence to cGMPs and regulatory standards throughout the product development lifecycle. This position offers an exciting opportunity to work with cutting-edge cell therapies in the oncology sector.

Skills & Requirements:

• Bachelor's degree in biology, Microbiology, Chemistry, or related field.
• Experience in cGMP Quality Assurance in Biologics or Cell & Gene Therapy manufacturing.
• Knowledge of current GMP regulations in pharmaceuticals and cell/gene therapies.
• Understanding of Quality Management Systems and ability to make informed decisions.
• Local travel between manufacturing sites is required.

The Quality Assurance Specialist's responsibilities will be:

• Issue, review, and approve GMP documentation such as batch records and SOPs.
• Review and reconcile logbooks and documentation.
• Assist in walkthroughs with senior Quality staff.
• Review labeling and packaging batch records for release preparation.
• Evaluate work orders, equipment qualification, and validation documentation.
• Ensure compliance and accuracy in batch record documentation for drug substance/product release.
• Provide daily onsite quality oversight and guidance, collaborating across functions.
• Represent QA in operations from starting material thaw to product filling and labeling.
• Perform additional duties as assigned.

If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at j.cerchio@proclinical.com

À±½·ÊÓƵ is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

À±½·ÊÓƵ Staffing is an equal opportunity employer.