QC Chemist (Testing) - 15 months training programme

Work location: Tuas, Singapore

At Pfizer Singapore, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. We strive to set the standard for quality, safety and value in the discovery, development and manufacture of health care products. Our global portfolio includes medicines and vaccines as well as many of the world's best-known consumer health care products. Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our time. Consistent with our responsibility as one of the world's premier innovative biopharmaceutical companies, we collaborate with health care providers, governments and local communities to support and expand access to reliable, affordable health care in Singapore.

Responsibilities:
· 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.
· Perform / review and document equipment verification and calibration in accordance to procedures.
· 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. ​
Must-Have
· Bachelor's Degree in Science
· Demonstrated technical skills in method validation and testing
· Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations
· Knowledge of Good Manufacturing Practices and its application standards, processes and policies
· Excellent organizational skills and strong ability to multi-task
· Strong written and verbal communication skills
· Ability to be flexible on shift (12-hr day/night) assignment
Work Location Assignment: On Premise