Our client is a professional Biotechnology and Pharmaceutical organization, based in Nordrhein-Westfalen Germany.
Our client manufactures Pharmaceuticals at their site in Nordrhein-Westfalen.
- Management of QA processes between production and QA - Ensuring GMP compliance
- Internal and External Audit guidance and tasks such as CAPA management - Setup and revision of SOPs and relevant quality documentation - Qualification of equipment and cleanrooms - Qualification documentation development and set up of infrastructure for DQ/IQ/OQ processes - Training of staff in GMP processes - Support production with Quality documentation such as Batch Record Review the following deviations in collaboration with production chemists.
- Educated as Chemist, Biologist or Pharmaceutical Technologist or related - Several years of QA experience - Strong team-player - Excellent English & German Skills
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.