Senior Qc Analyst

2 days ago

Singapore PFIZER ASIA MANUFACTURING PTE. LTD. Full time

**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

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