Job Description

Why Patients Need You
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
Your prior work experience and ability to apply your breadth of knowledge will help you adapt the standard methods and procedures. You will help us identify required delivery and process improvements that drive increased efficiency, throughput and quality. You will arrive at decisions on which methods and procedures are the best fit for different work situations.
It is your hard work and commitment that will make Pfizer ready to achieve new milestones and help patients across the globe.

How You Will Achieve It

Qualifications
Position Summary:
The incumbent is a member of the Quality Control (QC) Laboratory team. Under the supervision of the QC Manager / Supervisor, the key responsibilities are:

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  Perform / review and document analytical testing and results accurately and in accordance to test methods, site SOPs and relevant protocols, adhering to ALCOA principles and Data Integrity (DI) requirements.
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  Assist in troubleshooting laboratory technical problems and support laboratory investigations.
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  Perform preventive maintenance or calibration of instrumentation as required, undertake housekeeping responsibilities and follow safety regulations.
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  Use Imex "way of working" for day to day operations, problem solving, escalation and continuous improvements.

Responsibilities:

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  Perform / review and document analytical testing and results accurately and in accordance to test methods, site SOPs and relevant protocols, adhering to ALCOA principles and Data Integrity (DI) requirements.
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  Perform / review and document equipment verification and calibration in accordance to procedures.
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  Highlight any abnormalities detected during testing / review and raise laboratory investigations as required.
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  Support laboratory investigations and perform equipment troubleshooting where required.
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  Participate in 5S team initiatives and practice good housekeeping, ensuring all safety procedures are followed.
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  Author GMP documentation (e.g. operational procedures) as required.
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  Conduct training for fellow QC colleagues.
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  Uphold Pfizer\'s code of conduct and values.
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  Collaborate with cross-functional teams to drive flawless execution.
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  Play an active and impactful role in Tier processes by updating performance against metrics, highlighting issues, with appropriate escalations. Support development and implementation of solutions.
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  Contribute to the continuous improvement activities in QC laboratory or cross functional teams as nominated.

Must-Have

• High School Diploma or GED
• 4+ years\' experience
• Certification in assigned area, if applicable
• Successful hands-on analytical testing experience in a Good Manufacturing Practices {also cGMP} environment
• Technical Skills- Knowledge of laboratory equipment, testing and technique
• Basic math skills and computer skills, such as data entry, along with a high level of attention to detail
• Strong organizational skills and ability to multi-task across projects and activities
• Must be self-motivated and work with minimal direction
• Ability to read, communicate understanding and follow written procedures

Nice-to-Have

• Bachelor\'s Degree
• Demonstrate proficiency in computerized systems, such as Laboratory Information Management System

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