Senior QC Analyst

Every day, Pfizer’s unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting the patient first. Whether you are involved in development, maintenance, compliance, or research analysis, your contribution directly impacts patients. 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. Assist in troubleshooting laboratory technical problems and support laboratory investigations. Participate in 5S team initiatives and practice good housekeeping, ensuring all safety procedures are followed. 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 support laboratory investigations as required. Assist in equipment troubleshooting where required. Participate in 5S team initiatives and practice good housekeeping, ensuring all safety procedures are followed. Author GMP documentation (e.g. operational procedures) as required. 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)Diploma in Science (preferably related to Chemistry) or Chemical Process Technology. 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. 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 Use Your Power for Purpose Every day, Pfizer’s unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting the patient first. Whether you are involved in development, maintenance, compliance, or research analysis, your contribution directly impacts patients. 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. Assist in troubleshooting laboratory technical problems and support laboratory investigations. Participate in 5S team initiatives and practice good housekeeping, ensuring all safety procedures are followed. 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 support laboratory investigations as required. Assist in equipment troubleshooting where required. Participate in 5S team initiatives and practice good housekeeping, ensuring all safety procedures are followed. Author GMP documentation (e.g. operational procedures) as required. 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)Diploma in Science (preferably related to Chemistry) or Chemical Process Technology. 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 About Us #J-18808-Ljbffr