GMP Coordinator | Pharmakant (m/w/d)
CSL Behring GmbH
Job Summary
This full-time, permanent role is based at the Plasma Logistic Center in Schwalmstadt, where you will serve as a critical link in maintaining Good Manufacturing Practice (GMP) standards. Your day-to-day responsibilities involve creating, maintaining, and archiving essential GMP documentation, including SOPs, test instructions, and production protocols for both routine processes and global projects. You will act as a coordinator between your operational department and Quality Assurance, ensuring all documentation aligns with European and American regulatory requirements. A unique aspect of this position is the high level of international collaboration, requiring frequent communication with global quality units in English. You will also play a key role in monitoring compliance, reporting irregularities, and assisting with deviation management and corrective actions. This is an attractive opportunity for an experienced professional to join a global leader in biotherapeutics and contribute to the production of life-saving plasma-derived therapies.
Required Skills
Education
Completed 3.5-year vocational training as a Pharmaceutical Technician (Pharmakant) or equivalent, plus specialized internal GMP training.
Experience
- 4-5 years of professional experience in a pharmaceutical or GMP-regulated environment
- Professional experience in creating and maintaining GMP-relevant documentation
- Experience in coordinating with quality assurance units and global stakeholders
- Experience in handling deviations and implementing corrective measures
Languages
Additional
- The role requires familiarity with international regulatory standards (European and American authorities). Must be able to work on-site in Schwalmstadt on a full-time basis.