Qc Manager
6 days ago
summary
The incumbent is member of the Quality Control (QC) Laboratory team. Under the supervision of the Senior QC Manager,
the incumbent will be responsible for the operational aspects of all analytical testing within the QC Laboratory. Key
accountabilities include:
Lead, coach and develop the QC personnel (analysts, chemists and/or microbiologists) to ensuring that analytical
testing (chemical, physical and/or microbiological) and data review is performed in a safe and reliable manner to
support manufacturing operations across all shifts with adherence to site Standard Operating Procedures (SOPs).
Ensure that the quality systems and practices in the laboratory comply with Good Laboratory Practices (GLPs),
Good Documentation Practices (GDPs), current Good Manufacturing Practices (cGMPs) and Pfizer Quality
Standards (PQS).
Deploy and use Imex "way of working" for day to day operations, problem solving, escalation and continuous
improvements.
Responsibilities
Develop, review and/or approve working procedures for the laboratory.
Review analytical test results (e.g. product and raw materials)
Conduct, review or approve laboratory investigations and ensure all follow up actions are completed. Make decisions
based on scientific and logical reasoning on behalf of the Senior QC manager when required.
Supervise QC personnel in operational aspects of performing testing, e.g. troubleshooting laboratory equipment failure
and laboratory investigation..
Train fellow colleagues on written procedures pertaining to equipment operation, test methods and general laboratory
operation.
Conduct training to increase staff knowledge and understanding of Good Manufacturing Practices (GMP) and Good
Laboratory Practices (GLP) requirements, product chemistry and sophisticated laboratory equipment.
Lead or participate in site teams/projects e.g. NPI, continuous improvement, safety-related initiatives.
Supervise the team of analysts, chemists and/or microbiologists to ensure that DI and ALCOA principles are adhered to.
Minimum 8 years of technical experience in Quality Control within the pharmaceutical, food, chemical or process
industries. Additional experience in Quality Assurance is highly desirable.
Experience in managing/supervising large (8-12) groups of laboratory analysts, chemists and/or microbiologists.
Successful track record of continuous improvement, development and/or implementation of best practices in
Quality Control Laboratories.
Effectively communicate through written and oral means, demonstrated ability to interact effectively with senior
management, auditors and regulators.
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