Qc Manager

5 days ago


Singapore PFIZER ASIA MANUFACTURING PTE. LTD. Full time

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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