Responsible Person

Updated: May 11, 2024 02:17 AM GMT

Docpharm GmbH

Weil der Stadt

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... More Detail