Our client is a professional Biotechnology and Pharmaceutical organization, based in Schleswig-Holstein Germany.
Our customer is a Pharmaceutical company in Northern Germany
- Maintenance and development of the QMS - Support the QA Director with the quality strategy and management of the QMS
- Perform internal and external audits on a various topics - (re)write SOP's and support the regulatory department - Management of audits and inspections of the regulatory authorities - Follow up on audits and other quality tasks - Implement CAPA
- At least 5 years of experience in highly regulated environment - Experience in GMP environment (other GxP of added value) - Fluent in German and English - Travelling involved (indication at 30%)
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact admin admin.