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.

What You Will Achieve

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)

• Able to work in shift (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.
• Degree in Science (Chemistry)

Bonus Points If You Have (Preferred Requirements)

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

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