Responsible Person

vor 6 Monaten


Weil der Stadt, Deutschland Docpharm GmbH Vollzeit

To ensure the management of authorised activities and quality records are maintained accurately.
- Co-ordinating with manufacturers and promptly performing any recall operations
- Conducting the suppliers and customer audits as per the procedures
- To ensure that the self-inspections are performed at appropriate regular intervals following a pre-arranged 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 sub-contractors
- 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:

- 71263 Weil der Stadt (required)

Ability to Relocate:

- 71263 Weil der Stadt: Relocate before starting work (required)

Work Location: In person


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