Quality Control Supervisor – QC Department

About the role

The Quality Control (QC) Supervisor supports the QC Head in ensuring that all QC processes for material acceptance, batch release, and equipment validation are performed in full compliance with cGMP regulations, corporate standards, and national guidelines.

Key responsibilities

• Act as deputy to the QC Head, coordinating analytical activities for batch release and raw‑material/packaging acceptance.
• Maintain, review and approve QC records such as logbooks, forms and analytical batch records.
• Ensure adequate stock of reagents, standards and proper storage, labeling and monitoring of QC materials.
• Investigate out‑of‑specification, out‑of‑trend, out‑of‑expectation results and deviations, and verify implementation of CAPAs.
• Validate all QC methods according to SOPs, MA and cGMP requirements.
• Draft, review and update SOPs, protocols and reports; support stability program documentation and annual product review.
• Oversee training of QC analysts and manage QC technicians’ shifts and performance.
• Participate in internal self‑inspections and external audits, contributing to the local quality system.
• Lead projects related to new or existing products and ensure Good Laboratory Practice and HSE compliance.

Required profile

• Scientific degree, preferably in Chemistry or equivalent.
• Strong experience in a Quality Control department within a regulated environment.
• Fluent Italian and good written and spoken English.
• Ability to collaborate openly, communicate clearly and act with a sense of urgency.

Required skills

• Analytical method validation
• QC equipment qualification
• Stability testing
• Handling of radioactive materials
• cGMP compliance