Sr Qc Manager

2 weeks ago

Singapore PFIZER ASIA MANUFACTURING PTE. LTD. Full time

summary

The incumbent will be responsible for overall management of the Quality Control (QC) Laboratory services and their related

support teams. With extensive knowledge of compliance requirements relating to the QC function together with excellent

verbal, written, and interpersonal communication skills the incumbent will need to be action-orientated, agile with respect to

change management and a strong leader for the quality culture of the Laboratory and the site to achieve the site Quality

Control operational objectives. Key accountabilities include:

Lead, coach and develop a team of QC Managers, supervisors and their related laboratory teams ensuring that

analytical (physical, chemical and microbiological) testing, data review activities and Laboratory equipment and

systems on site comply with site Standard Operating Procedures (SOPs) and are performed in a safe and reliable

manner to support manufacturing operations at the site and across all shifts.

Ensure that the quality systems in the Laboratory are continually audited with new requirements implemented and

all QC related operations 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:

Responsible for developing and managing integrated Quality Systems and providing technical support and advice on

Quality Control matters to other areas within the site: Production, Procurement, Supply Chain, Warehouse, and Process

Development.

Responsibility of setting up and implementing QC Laboratory quality systems and strategies for developing and

implementing monitoring systems to collect, collate and present information on Quality Control Laboratory for

performance management and bench marking. This includes review and approval of Standard Operating Procedures

(SOPs) and periodic review processes.

Responsibility for QC personnel management, QC project management, and ensuring that quality risks associated with

the QC Laboratory operations are correctly assessed, identified and managed.

requirement

Minimum 8-10 years of technical experience in Quality Control within the pharmaceutical, food, chemical or process industries. Additional experience in Quality Assurance is highly desirable.

Minimum 5 years in a leadership/supervisory position of professional staff previously, or demonstrated capability to successfully lead large teams.

Successful track record of continuous improvement, development and/or implementation of best practices in Quality Control Laboratories.

Experience in an API manufacturing plant is preferred.

Effectively communicate through written and oral means, demonstrated ability to interact effectively with senior management, auditors and regulators.

Bachelor or Master or Ph.D. degree in Science (Chemistry preferred) or Life Sciences relating to Chemistry, Pharmacy, Pharmaceutical Sciences or Microbiology or a related science.

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