**Your responsibilities:**
- Support in transfer and implementation of troubleshooting analytical methods
- Further development of cGMP compliance
- Handling deviations and OOS procedures, conducting investigations into deviations and OOS procedures
- Creation and monitoring of the implementation of CAPAs
- Planning of audits and addressing findings from audits in collaboration with the Head of QC Operations
- Participation in the creation of template documents such as SOPs and testing instructions
- Rejection or approval of starting materials, packaging materials, active ingredients, and finished pharmaceuticals as a representative of the Head of Quality Control
- Review and approval of test protocols/batch records
- Optimization of laboratory processes to increase productivity and improve quality (e.g. process improvement, method optimization, KPI selection, and improvement, standardizations in collaboration with laboratory personnel and managers, automation and digitalization in the laboratory area)
- In addition, there is the option to take over the management of the laboratory after training.
**Ideal profile**
- Successfully completed a natural science degree.
- Ideally five years of professional experience in the pharmaceutical industry.
- Leadership experience is an advantage.
- Experience with chemical-physical and instrumental analysis methods in the (radio) pharmaceutical industry.
- Thorough GMP knowledge.
- Excellent communication skills in German and English.
