Responsible Person - Weil der Stadt, Deutschland - Docpharm GmbH

Beschreibung

To ensure the management of authorised activities and quality records are maintained accurately.

• Coordinating with manufacturers and promptly performing any recall operations
• Conducting the suppliers and customer audits as per the procedures
• To ensure that the selfinspections are performed at appropriate regular intervals following a prearranged programme and necessary corrective measures are put in place.
• To ensure and approve final disposition of returned, rejected, recalled or falsified products are dealt with effectively.

- approve any returns to saleable stock, providing quality support and oversight for Distribution Operation review meetings with Distribution contractors.

• Contribute to defining GMP, quality, KPI's and ot review quality indicators with recommendations for actions for improvement in regards to GMP guidelines.
• Ensuring CAPA's are identified, effective temperature control of medicines, temperature mapping.
• Ensuring annual GMP, initial and continuous training programmes are implemented and maintained to all employed staff.
• Ensure Quality Technical Agreements are in place for all outsourced activities and with all subcontractors
• Ensure that the Parallel Import design and relabelling is according to the EU GMP standards
• Maintaining required documentations and licenses for the processing of these licenses.

Salary:
From 50.000,00€ per month


Experience:

• RP: 5 years (required)

Ability to Commute:
Weil der Stadt (required)


Ability to Relocate:

Weil der Stadt:
Relocate before starting work (required)


Work Location:
In person