Your responsibilities:
* Ensure cGMP compliance and timely quality control of medicinal products and supplements
* Manage and develop employees, as well as supervise laboratory units
* Monitor and optimize processes, while training subordinates in laboratory analysis
* Ensure on-budget and on-time release of products and QC turnaround times
* Prepare and monitor internal and external audits, and support QC management in budget planning
Your profile:
* Completed science degree with specialized knowledge of analytical technologies, particularly HPLC, GC, and pharmacopoeia analysis.
* Several years of experience in pharmaceutical control laboratories and knowledge of normative requirements from the medical device sector
* Strong leadership, communication, and decision-making skills with a high level of initiative and entrepreneurial action.
* Implementation strength, high resilience, and flexibility with an independent and structured way of working.
* Proficient in English and safe handling of common software programs (Office 365, SAP).
