pfizer
Senior QA Specialist (Investigations)
At a Glance
- Location
- Singapore - Tuas, Singapore
- Employment
- Full time
- Experience
- 4+ years
- Posted
- 2026-08-14
Key Requirements
Domain Knowledge
- Engineering
- Pharmaceutical
- Regulatory
Requirements
Demonstrates a proactive mindset and commitment to delivering high-quality outcomes.
Adopts digital technology to improve the speed, scale, and effectiveness of interactions and actions.
Minimum of 4 years of experience, including QA experience, within the pharmaceutical industry.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on

Quality Assurance and Control
Responsibilities
The incumbent is a member of the Quality Assurance (QA) Operations team.
Under the supervision of the Senior QA Manager, the incumbent will be responsible for the following:
Provide Quality Assurance (QA) oversight of Good Manufacturing Practice (GMP) investigations, including manufacturing and laboratory investigations, to ensure products comply with Pfizer Quality Standards (PQS) and International Council for Harmonisation (ICH) guidelines.
Serve as the local process owner for investigation-related quality systems, including Nonconformance, Corrective and Preventive Actions (CAPA), and Management / Board of Health Notifications.
Maintain awareness of regulatory expectations and support site inspection readiness.
Promote a strong quality culture and GMP-compliant behaviours at the site.