Pfizer

Use Your Power for Purpose

Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard.

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:

• 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.
• Highlight any abnormalities detected during testing / review and raise laboratory investigations as required.
• Assist / troubleshoot laboratory technical problems.
• Author SOPs, analytical method transfer protocols and reports and other GMP documentation (e.g. trend reports).
• Use Imex "way of working" for day-to-day operations, problem solving, escalation and continuous improvements.

Responsibilities

• Perform / review and document analytical testing (In-Process, Raw Materials, API samples) and results accurately and in accordance to test methods, site SOPs and relevant protocols, adhering to ALCOA principles and Data Integrity (DI) requirements.
• Highlight any abnormalities detected during testing / review and raise laboratory investigations as required.
• Support laboratory investigations and perform equipment troubleshooting where required.
• Participate in 5S team initiatives and practice good housekeeping, ensuring all safety procedures are followed.
• Author SOPs, analytical method transfer protocols and reports and other GMP documentation (e.g. trend reports).
• Set up and maintain QC processes (e.g. reference standards and retention sample management), perform investigations as required for any associated deviations.
• Conduct training for fellow colleagues from QC and other departments (e.g. Production).
• Uphold Pfizer's code of conduct and values.
• Collaborate with cross-functional teams to drive flawless execution.
• 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.
• Contribute to the continuous improvement activities in QC laboratory or cross functional teams as nominated.

Here Is What You Need (Minimum Requirements)

• Degree in Science (Chemistry)
• Able to work in shift (for IPC team)
• Effective problem solving skills.
• Demonstrated ability to perform in a team.
• Knowledge of cGMPs and ALCOA principles.
• Possess a can-do / pride to succeed attitude.
• Embrace the use of digital technology to scale and speed up every form of interaction and action.

Bonus Points If You Have (Preferred Requirements)

• A minimum of 1 year QC experience in an analytical laboratory is preferred.

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.

Quality Assurance and Control

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