Pfizer Hiring For Lead Laboratory Analyst at Tuas Full Time

Lead Laboratory Analyst

Pfizer–Tuas

About 2 hours ago, from Pfizer Global

Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients.  Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.

What You Will Achieve

You will be recognized as a subject matter expert with specialized knowledge and skills in procedures, techniques, tools, materials and equipment. You will be entrusted with adapting standard methods and procedures by applying your knowledge, prior work experience and requirements. Your business awareness of cross-organizational impact on project delivery will elevate the quality of project deliverables. You will arrive at decisions on which methods and procedures are the best fit for different work situations.

You will train others and reinforce behaviors that will help us achieve our goal of providing the best healthcare to our patients.

How You Will Achieve It

• Assign Standard Work activities by prioritizing according to laboratory demand and available resources when stand in as QC Supervisor.
• Monitor the laboratory status and liaise with colleagues of other departments to ensure there is no interruption to manufacturing process when stand in as QC Supervisor.
• Stand in for QC Supervisor when they are absent from work or when they are on project assignments.
• Provide advice, guidance, support and training to team members in order to improve the teams’ capability.
• Develop working process to enhance GMP standards for the team.
• Develop On Job Training (OJT), Job Safety Aassessments (JSAs) and Risk Assessments (RAs) for laboratory operations.
• Conduct OJT training for new hires.
• Troubleshoot all operating deviations and issues and coordinate with other function when required.
• Perform chemical analysis using wet chemistry methods and analytical instrumentation, including HPLC, GC, particle size analyzer etc.
• Ensure that tests assigned are performed in a timely manner in accordance with validated test protocols and procedures.
• Perform instrument calibration, maintenance and troubleshooting. Able to prioritize based on operation needs.
• Support laboratory operations, including sample receipt, sample subdivision and labeling, waste disposal, stability sample packing.
• Advise on the significance of test results and follow up with appropriate course of actions.
• Actively participate in Safety initiatives, typically a role model for other analyst. Ability to perform investigation related to EHS.
• Participate in 5S team initiatives and practice good housekeeping.
• Coordinate work flow and laboratory activities according to QC sample and testing plans.
• Lead and conduct laboratory investigations/incidents such as out of specification investigation and equipment troubleshooting investigations, identify root causes and implement appropriate corrective action and preventive measures.
• Participate in Analytical Method Transfer Exercise and independently resolve issues associated with test methods
• Review test reports and ensure that all laboratory documents are in a constant state of regulatory compliance and inspection readiness.
• Develop test methods or instrument Standard Operating Procedures (SOPs), write and update Quality Procedures.
• Plan and deliver technical training to colleagues. Developed and review training materials as required e.g. Basic lab techniques.
• Close coordination with cross function colleagues / Vendors to achieve desire outcome ( e.g. Lab equipment installation/ Validation/ Service contract / External contract lab testing fulfillment).
• Commitment to work and positive influencer/role model/motivate others for overall operational excellence.

Qualifications

• Diploma in Science (preferably Chemical Process Technology) or equivalent
• Minimum 5 years of quality control experience in the pharmaceutical industry.

Work Location Assignment: On Premise

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

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