Description
Job Description:- To act as a QP in the Batch Release group
- Certify medicinal product in accordance with requirements of product marketing authorization, EU Directive /EC & /EC and EU GMP Annex 16.
- Assist in the coordination of the QA operational duties relating to product disposition.
- Participate in investigations and risk assessments related to manufacturing deviations and changes and ensuring appropriate actions are implemented.
- Coordinating deviation investigations, log trend deviations and issuing regular reports on such trends.
- Advising and providing input into quality systems across the plant.
- Coordinating sampling activities for incoming materials
- Coordinating the on-line inspections of packed product
- QA review of documentation, including SOP's, worksheets, logbooks.
Essential Skills:
- At least 5 years working within a pharmaceutical manufacturing environment in a Quality capacity.
- BSc (hons) Degree in related discipline along with MSc or Post grad which leads to QP status.
- A minimum of 2 years experience working as a QP on a manufacturing license.
- Previous experience in a Pharma Solid Dosage environment would be beneficial
If you would like to know more about this position please contact me on or reply with a copy of your CV. We also offer shopping vouchers for any successful referrals.