A house hold name in the pharmaceutical market are currently recruiting for a Qualified Person (QP) to join their UK division, to provide Quality assurance expertise working on various products. Acting as lead for compliance dictated to by regulations, standards and law in the batch release of products both here in the UK and across Europe.
The ideal person will be a current QP who has overseen and contributed in batch releases (Oral solid dose, Oral Liquid Dose and Semi Solid Dose), contributed in change control requests, technical agreements analytical method transfers as well as someone who has experience in leading both external and internal audits. Must be willing to be hands on and carry out other Quality responsibilities all the way down to investigating CAPAs.
Essential Experience:Have held a QP Position in an organisation relating themselves to the Pharmaceutical industry.
Had experience in Batch Releases across Europe
Can independently review and approve quality documents such as change control requests, technical agreements, analytical method transfers, NCRs, PQRs, SCs, APQRs, risk assessments and data-logger statements.
Able to lead both internal and external audits.
Analytical thinking who has the confidence to make judgment calls and decisions at high levels.
Must be clued up on regulatory requirements to ensure company is working inline.
Well adverse to handling recall on product if needed.
This is a fantastic opportunity to join a global company in a very autonomous senior role. With the opportunity to coach and mentor staff beneath you a pave a way for the quality departments future direction. This is an office-based position where COVID measures are in place to protect all staff.
- Agency: Cpl Life Sciences
- Contact: Sheldon Grant
- Reference: JO-2107-472225
Website: Cpl Life Sciences
- Posted: 9th July 2021
- Expires: 6th August 2021