QA QP - Qualified Person- Pharmaceuticals - East Midlands


An exciting opportunity has arisen for a QA QP to join a reputable consultancy that provides support to the Human and Veterinary Pharmaceutical Industry. This consultancy provides services in Technical, Manufacturing, Regulatory, Development and QP Batch Release.


As a QA QP your responsibilities will involve (but not limited to):
*Acting as a QP (Qualified Person)
*Reviewing relevant documentation associated with manufacturing and testing of Pharmaceutical products
*Providing Quality System Support
*Addressing queries regarding GMP certification and batch release
*Actively managing assigned areas of the QMS
*GMP auditing of API, finished product and packaging supplier
*Internal/External Auditing
*Consistent involvement with customers
*GMP subject matter expert


Skills/Expertise/Education Required:
*Degree educated in a scientific discipline
*QP Status, and experience on a manufacturing license
*Experience in GMP for Solid Dosage Forms (Tablet, Capsules) and injectables.
*Experience in Dossier Developments and input in to technical aspects would be desirable
*GMP auditing experience of API
*Experience of 3rd party manufacturing outside the EU would be advantageous


If successful you will be rewarded with a generous salary and benefits package, including a profit sharing bonus. This role would suit an individual who is seeking a diverse role, and open to travel both in Europe and India when required. There is home working on offer for the successful candidate.

If you have the drive and enthusiasm to be a part of this exciting opportunity, please contact Nisha Rai, Recruitment Consultant at Paramount Recruitment 0121 616 3468

Keywords: QP, Qualified Person, QA, Quality Assurance, Pharmaceutical, Manufacturing, Consultancy Services, Regulatory, GMP, Solid Dose Forms, Injectables, Auditing, Dossiers, Internal, External, Technical Transfer, Product Design, Batch Release, QMS, API, Packaging, East Midlands, Europe, EU, India, England




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