Pfizer are currently seeking to recruit a QA team lead.
To partner with the OpU functional area personnel to ensure that products are manufactured and tested to cGMP requirements and to support the compliant manufacture, review and disposition of these products, in addition to managing, coaching and supporting a QA Operations team.
Provide quality and compliance support to the Operating Unit, ensuring appropriate GMP requirements are met for the commercial operations, including QA and technical support of product transfers and the associated validation of product, process, equipment and facility, as necessary.
Manage the review and disposition of commercial and PV batches, in liaison with the appropriate QP, to ensure disposition & project schedules are met.
Education & Experience
Pharmacy degree or B.Sc. degree in science discipline plus a QP post grad qualification i.e. Candidate must be eligible to become a Qualified Person (QP)
Significant QA/QC/Compliance experience in a pharmaceutical, or bio-pharmaceutical manufacturing environment.
Five+ years experience in a Pharmaceutical Management position. Experience in managing managers or QP’s would be an advantage
For a copy of the full job description please email firstname.lastname@example.org. All correspondence will be held in the strictest of confidence.
The Global Established Products (GEP) division are recruiting for two positions - Senior Regulatory Affairs Executive and Regulatory Affairs Executive. Closing date 20th May 2016.
For further details, see Pfizer Regulatory Affairs roles May 2016.
Posted 8th May 2016