Your mission

• Contribution to the Continuous Improvement of the Corporate Midas Pharmaceutical Quality System.
• Management of international GxP and Regulatory standards during sourcing, development, procurement, manufacturing and supply chain of Drug Substances (IM, API) and Medicinal products (FDF). 
• 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.
• Securing the high Midas compliance level with regard to international cGMP regulations (e.g. EU, US, AUS)...