Corporate Quality Manager (all genders)

Das ist der Job

Your mission Contribution to the Continuous Improvement of the Corporate Midas Pharmaceutical Quality System.

Darum lohnt es sich

Management of international GxP and Regulatory standards during sourcing, development, procurement, manufacturing and supply chain of Drug Substances (IM, API) and Medicinal products (FDF). Securing the high Midas compliance level with regard to international cGMP regulations (e.g.

Participation and Coordination of Corporate Quality Management activities; QM Compliance Process Responsibilities; e.g. Document management, Change control, Deviation, Complaint, CAPA, Trainings Communication with the manufacturing and development partner and reviewing, advising and compiling of GxP and regulatory relevant documents.

Product Life Cycle Management; Registration, Coordination, Evaluation and follow-up of Changes, Non-conformities which appear in the framework of internal as well as external established processes. EU, US, AUS) Cooperation in inter-divisional, Midas Pharma group-wide and / or cross-company projects.

Supplier Qualification including documentation, coordination and follow-up of supplier and product documentation such as (but not limited to) Drug Master Files, Dossiers, Site Master Files, Validation documents.

Communication with the manufacturing and development partners and reviewing, advising and compiling of GxP and regulatory relevant documents and certificates. Audit/Technical Visit of suppliers Regular business trips. Your profile Graduation in Science e.g.