Our client a, patient-centered, clinical-stage biopharmaceutical company focused on developing cell therapies for patients suffering from autoimmune diseases seeking a QA Person In plant to join their growing team.
Responsibilities :
- Perform batch record review of investigational products manufactured at CMO partners.
- Perform QA / client review for internal and / or CMO Quality System records, manufacturing documents, analytical methods, and qualification / validation documentation.
- On-site oversight of CMO operations as needed.
- Ensure all necessary documents / forms / records are authorized to facilitate movement of cell product to clinical sites
- Support Manufacturing to collect and monitor key performance indicators of CMO and contract / external laboratories.
- Review, maintain, and execute against Quality Agreements with the Supplier / CMO network.
- Ensure issues are identified and managed through to resolution in a timely manner and deliverables are met as required.
Skills :
8+ years of pharmaceutical manufacturing and / or Quality Assurance experience, with at least 2 years' experience in the field of cell therapies preferred.Expertise with cGMP manufacturing as well as global regulatory regulations and requirements for biopharmaceutical products and ATMPsAbility to operate in a Controlled / Classified Environment, including ability to successfully maintain aseptic technique and complete cleanroom gowning qualification requirements.Demonstrated ability to manage multiple complex relationships within a CMO networkExperience with electronic Quality Management SystemsExperience in conducting or hosting Quality and / or Health Authority audits.Education :
Degree (Bachelors or higher) or equivalent experience in life sciences, Biology, Biochemistry, Chemical Engineering, Biotechnology