About the role
AI summarisedThis 15-month Career Progression Program offers a distinguished talent development initiative within the Quality Assurance team at Pfizer's Tuas manufacturing site. The role is crucial in driving quality culture, ensuring compliance with global standards, and supporting regulatory readiness for advanced biopharmaceuticals manufacturing.
BiopharmaOnsite
Key Responsibilities
- Review and approve GMP documentation ensuring compliance with PQS/Global Policies/SOPs/Work Instructions.
- Conduct internal audits and support external audits to ensure effective internal controls and vendor oversight.
- Manage logistics for internal and external GMP inspections, maintaining inspection readiness at all times.
- Facilitate regulatory submissions and address agency queries accurately and in a timely manner.
- Participate in gap analysis of site procedures against PQS and propose corrective actions to mitigate risks.
- Maintain quality tracking systems and metrics to proactively identify trends and atypical observations.
- Support Quality Management Review (QMR) meetings and contribute to Tier processes.
Requirements
- Eligibility: Singapore Citizens or Singapore Permanent Residents.
- Program Duration: 15 months training programme.
- Fresh graduates are welcome; Mid-Career candidates must have graduated at least 2 years prior to application.
- Strong verbal, written communication, and presentation skills are essential.
- Demonstrated ability to work effectively within a cross-functional team.
- Ability to act independently to resolve issues while knowing when and how to escalate.
- Commitment to upholding Pfizer's code of conduct and values.