Lead and develop the GMP unit and quality control laboratory in Rotterdam. Manage a team, improve compounding and QC processes, uphold CGMP standards, and coordinate multidisciplinary technical projects.
The role
At our client company in Rotterdam, you will be responsible for leading and further developing the GMP unit and quality control laboratory.
Responsibilities
- Lead a team of pharmacy assistants, production employees and analysts, ensuring optimal staffing and planning.
- Turn strategic objectives into concrete improvement projects and process optimisations for compounding and quality control.
- Coach employees in collaboration, ownership and results, and promote professional conduct.
- Ensure CGMP and quality standards are upheld and work closely with pharmacists and partner departments.
- Coordinate multidisciplinary technical projects involving process-related, mechanical and electrical modifications. You will be involved from the costing and tender stage through handover and aftercare, with a focus on partner hospitals and internal production processes.
Time allocation
- Approximately 40% project coordination.
- Approximately 25% technical subject-matter coordination.
- Approximately 15% planning and budget monitoring.
- Approximately 10% commercial coordination.
- Approximately 10% administration and reporting.
Requirements
The available information does not specify formal education, work experience or certification requirements.
Conditions and schedule
The contract type, working hours, salary and shift pattern are not specified in the available information.