QC Supervisor

Job Description

Legend Biotech is seeking a QC Supervisor to oversee quality control for personalized cell therapy production in a GMP environment in Ghent, Belgium. The QC Supervisor will manage QC analysts and troubleshoot issues, working in shifts to ensure coverage for operational needs.

Responsibilities:

• Responsible for both IPC (in process analyses) as EMS (environmental monitoring).
• Read, interpret and revise documents such as SOPs, work instructions.
• Develop positive relationship with the QC team and other departments.
• Make appropriate and compliant GMP decisions independently.
• Resolve problems through the use of quality systems.
• Develop and implement improvement ideas.
• Support QC analysts team development.
• Generate shift schedules.
• Maintain individual training completion in a compliant state.
• Support corrective and preventive actions and internal/external audits.
• Review/approve documents as a Quality Control Subject Matter Expert (SME).
• Remain current in skills and industry trends.

Requirements:

• A minimum of a Bachelor’s Degree in Science, Information Science or equivalent technical discipline is required.
• A minimum of 6 years relevant work experience is required.
• Experience working in an aseptic manufacturing facility, preferably in quality control, quality assurance, manufacturing compliance, clinical quality, or cell therapy is preferable.
• A minimum of 2 years of experience with quality control is preferred.
• A minimum of 1 year of leadership experience is also required.
• Knowledge of cGMP regulations and FDA/EU guidance.
• Strong interpersonal and written/oral communication skills.

The role offers:

• Opportunity to work in a sterile GMP environment.
• Chance to support clinical and commercial requirements in cell therapy.
• Opportunity to lead and develop a QC team.