Senior Supervisor Quality Control Testing & Sample Management

About This Role:
As the Senior Supervisor of Quality Control Testing & Sample Management, you will be an essential part of the team at our manufacturing site, driving operational excellence in a GMP environment. You will lead a dedicated team, overseeing all sample logistics, management, and analytical testing processes. In this role, you will manage workflows, ensure regulatory compliance, and champion continuous improvement initiatives that align with our commitment to quality. Your responsibilities have a direct impact on product quality and compliance, making you a pivotal contributor to our success. You will collaborate with cross-functional teams to implement best practices and ensure seamless QC operations. This position is crucial for maintaining the integrity and efficiency of our laboratory support functions.

What You'll Do:

• Direct line management including performance management, capability development, and workforce planning.
• Planning, coordination, technical review, and approval of business critical QC testing, including TOC/Conductivity and PCR based assays, ensuring data integrity and regulatory compliance.
• Ensure GMP-compliant status of QC laboratory equipment and processes.
• QC representative during health authority inspections and internal/external audits.
• Oversee and continuously improve sample management activities, including handling, storage, and shipment of raw materials and drug substances.
• Manage retain samples and oversee shipment of stability samples to external sites.
• Drive continuous improvement initiatives to enhance efficiency and optimize resource utilization.
• Monitor and analyze key performance indicators to identify trends and improvement opportunities.
• Author, review, and approve complex GMP documentation.
• Participate in technology transfers for new product integrations.
• Collaborate with global QC networks to align best practices and regulatory standards.

• Bachelor's degree in Life Science or Technical discipline.
• Minimum 8 years of experience in a pharmaceutical, biotech, chemical, or food manufacturing environment.
• Proven experience in GMP Quality Control functions.
• Strong leadership and team management abilities.
• Excellent organizational, presentation, and communication skills.
• Proficiency in GMP documentation and process improvement methodologies.
• Ability to prioritize and multi-task in a fast-paced environment.

• Master's degree in a related field.
• Experience in personnel or project management.
• Familiarity with biopharma quality control practices.