We are a growing pharmaceutical company specialized in the manufacturing of sterile injectable products with terminal sterilization. We operate both as a manufacturer and as a Contract Manufacturing Organization (CMO), supporting international clients in the development and production of high-quality injectable medicines.
To strengthen our Quality Control Department, we are looking for an experienced and motivated QC Supervisor – Chemical Laboratory.”
Supervise compliance with EU, FDA, and other applicable regulatory guidelines within the QC department
Lead and manage analytical method transfers and suitability testing for new products
Supervise a team of QC analysts, ensuring high cGMP and GLP standards are consistently maintained
Ensure adherence to laboratory schedules and performance targets to meet regulatory and business requirements
Coordinate laboratory activities supporting raw materials, in-process controls, finished products, cleaning validation, and stability testing
Liaise effectively with Manufacturing, QA, Regulatory Affairs, and other departments to ensure timely completion of activities
Drive continuous improvement initiatives within the QC laboratory and quality systems
Support regulatory inspections and customer audits
Develop and maintain training programs, SOPs, validation documentation, and compliance systems
Provide day-to-day leadership, coaching, and performance management to QC staff (potentially across multiple shifts)
Promote a strong culture of quality, accountability, and safety
Previous supervisory or technical specialist experience in a pharmaceutical QC laboratory
Strong knowledge of cGMP, GLP, and regulatory requirements (AIFA, FDA, ISO standards)
Experience supporting customer and regulatory audits
Experience leading analytical project teams
Knowledge of SAP is considered an advantage
Fluent English (written and spoken)