QC Supervisor - Chemical

We are looking for an experienced Chemical Lab. QC Supervisor to oversee chemical quality control activities related to testing and release of incoming raw and packaging materials.

The role is responsible for ensuring the accuracy, reliability, and timely completion of laboratory testing, overseeing analytical methods and instrumentation, issuing Certificates of Analysis (COAs), investigating deviations and abnormal results, and ensuring compliance with GMP, GLP, GDP, ISO 17025, and applicable quality requirements.

The position will also lead a team of QC laboratory professionals and collaborate with cross-functional teams to ensure the timely availability and quality of materials required for manufacturing.

• Supervise and coordinate all chemical testing activities for incoming raw materials and packaging materials.
• Ensure that laboratory testing is performed accurately, efficiently, and according to approved specifications, methods, and procedures.
• Develop, optimize, and validate analytical methods for incoming raw and packaging materials.
• Establish, implement, and maintain QC laboratory procedures to ensure consistency, accuracy, reliability, and traceability of analytical results.
• Review and approve analytical test results and laboratory documentation.
• Review information related to received materials against relevant inspection reports and specifications.
• Analyze test results and identify deviations, anomalies, and out-of-specification or atypical results, ensuring appropriate investigation and corrective actions.
• Issue and review Certificates of Analysis (COAs) for raw materials and packaging materials in a timely manner.
• Establish and maintain effective systems for the calibration, maintenance, and proper operation of analytical laboratory instruments.
• Ensure laboratory instruments and equipment remain fit for purpose and compliant with applicable requirements.
• Prepare and present analytical reports, laboratory findings, and quality metrics to relevant stakeholders.
• Ensure compliance with GMP, GLP, GDP, and applicable QMS requirements.
• Ensure laboratory activities comply with applicable ISO 17025 requirements.
• Coordinate laboratory and facility accreditation activities related to ISO 9001, ISO 14001, ISO 45001, ISO 17025, ISO 50001, and GMP.
• Collaborate with QA, Production, Warehouse, Procurement, and other relevant departments to ensure the timely availability of approved, high-quality raw materials and packaging components.
• Identify opportunities for improving laboratory workflows, testing efficiency, turnaround time, and overall operational effectiveness.
• Ensure proper documentation and data integrity throughout all laboratory activities.
• Ensure adherence to company QHSE policies and procedures.
• Participate in emergency response activities according to the assigned responsibilities within the emergency plan.
• Supervise, coach, and develop QC laboratory team members to ensure effective performance and continuous technical development.
• Ensure team members are appropriately trained on laboratory procedures, GMP/GLP requirements, analytical techniques, and relevant quality standards.

Education

• Bachelor's degree in Science, Chemistry, Analytical Chemistry, Biochemistry, or a related scientific discipline.
• Additional qualifications or certifications in Quality Control, Analytical Chemistry, or Laboratory Management are an advantage.

Professional Experience

• Minimum 6 years of relevant experience in a QC laboratory within a pharmaceutical, biopharmaceutical, vaccine, or regulated manufacturing environment.
• Proven experience in chemical analysis and instrumental analysis.
• Previous experience supervising or leading QC laboratory personnel is strongly preferred.
• Hands-on experience with analytical method development and validation.

Technical Knowledge

Strong knowledge of:

• Chemical Analysis
• Instrumental Analysis
• Analytical Method Development
• Analytical Method Validation
• Raw Material Testing
• Packaging Material Testing
• Laboratory Quality Control
• Laboratory Instrumentation
• Instrument Calibration and Maintenance
• Specifications and Test Methods
• Certificate of Analysis (COA)
• GMP – Good Manufacturing Practice
• GLP – Good Laboratory Practice
• GDP / GDocP
• Data Integrity
• OOS / OOT Investigation
• Deviation Management
• Corrective and Preventive Actions (CAPA)
• ISO 17025:2017
• ISO 9001:2015
• ISO 45001:2018
• ISO 14001
• ISO 50001
• QHSE requirements
• Vaccine Manufacturing / Pharmaceutical Manufacturing

• Social, Medical and Life Insurance
• Pension Coverage
• Profit Share
• Quarterly Balance Scorecard
• Transportation to the nearest point