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Quality Control Supervisor

Job in Florence, Tuscany, Italy
Listing for: Galenica Senese S.r.l. Industria Farmaceutica
Full Time position
Listed on 2026-06-02
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
Job Description & How to Apply Below
Position: QUALITY CONTROL SUPERVISOR
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."

Key Responsibilities
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
Qualifications & Experience
Degree in Chemistry, Pharmaceutical Chemistry, or a related scientific discipline
Previous supervisory or technical specialist experience in a pharmaceutical QC laboratory
Experience in sterile injectable manufacturing is highly desirable
Strong knowledge of cGMP, GLP, and regulatory requirements (AIFA, FDA, ISO standards)
Experience supporting customer and regulatory audits
Proven experience in analytical method validation and transfer
Experience leading analytical project teams
Knowledge of SAP is considered an advantage
Strong leadership, communication, and organizational skills
Fluent English (written and spoken)
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