Qualified Person/QA Manager

Recruiter
CK Group
Location
Frankfurt ( Oder)
Salary
Up to €175,000 per annum
Posted
26 May 2021
Closes
23 Jun 2021
Ref
49621
Contact
Jim Gleeson
Contract Type
Permanent
Hours
Full Time
CK Group are recruiting for a Qualified Person/QA Manager to join a global clinical trial supplies logistics organisation, based at their site in Frankfurt.

Salary:

Base salary up to €175,000 per annum.

Qualified Person/QA Manager Role:
As Qualified Person/QA Manager you will be responsible for the quality aspects of IMPs requiring importation into the EU, QP confirmation or QP certification for release into the EU. You will also have responsibility for the quality testing and approval of incoming secondary packaging materials, incoming IMPs, Marketed Product, Products for Named Patient Programs and finished product from internal packaging operations.

Key duties will include:
  • Ensuring that all activities (storage, additional labelling, quality control, distribution, returns, rejects and destruction) related to IMPs, medicinal products used in clinical trials/NPPs and starting materials are performed in compliance with European and regional regulations and Good Manufacturing/Distribution Practices, as needed.
  • Hosting client audits and regulatory inspections and managing the audit report responses.
  • Implementation and maintenance an efficient system, handling documentation relating to Quality such as Procedures, Product Specification Files, Technical Agreements, Qualifications, Quality Systems etc.
  • Management of CAPA plans, collating CAPA data, and implementation of quality improvement initiatives.
  • Taking responsibility for and fulfilling the role of Head of Quality Control ('Leitung der Qualitätskontrolle') for the Frankfurt depot as per current German GMP guidance AMWHV.

Your Background:
As Qualified Person/QA Manager you will require:
  • Extensive experience of working with biological products is essential.
  • A relevant science degree.
  • Qualified Person status.
  • Extensive pharmaceutical industry based experienced of GDP, GMP and GCP regulations.
  • Proven problem solving, collaboration, negotiation, and conflict resolution skills.
  • Ability to travel as necessary.

Apply:
For more information or to apply for this Qualified Person/QA Manager position, please contact CK Group, quoting job ref 49621.

It is essential that applicants hold entitlement to work in Germany.

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