Qualified Person QP

Package: Up to £110,000
Industry: Sterile Manufacturing

As a Qualified Person (QP), you will be responsible for ensuring that batches of medicinal products are manufactured and assembled in compliance with GMP legislation. You will work closely with the clinical project team to ensure safe and efficient conduct of clinical trials. This is an excellent opportunity to develop your experience in clinical research regulatory matters.

In addition to the above responsibilities, the successful candidate will also be expected to act as a de facto quality manager/operations manager when the current QM is not on-site.

Qualified Person (QP) Responsibilities:

• Ensure compliance to Pharmaceutical Quality System
• Promote Quality Culture and identify GMP Quality improvements
• Work with Customers to set new supply chains and provide end-to-end QP support during sponsor clinical trials
• Review and approve deviations and non-conformances
• Maintain continuous professional development

Qualified Person (QP) Experience:

• Qualified person in accordance with Directive 2001/20/EC, and/or Qualified person in accordance with Directive 2001/83/EC
• BSc/MSc in Pharmacy or relevant scientific discipline
• Strong numerical skills required

If you are interested in this opportunity please apply now and I will be in touch.