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Pfizer is offering a 15-month Career Progression Program for QA Specialists in Singapore. This initiative aims to develop professionals in biopharmaceutical manufacturing. Participants will gain practical experience while ensuring GMP compliance and quality standards. Eligible candidates include those with relevant degrees or fresh graduates.
We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.
To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals.
Pfizer Global Supply proudly shoulders the responsibility of manufacturing and distributing our wide-ranging pharmaceutical products.
Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.
Transforming Delivery of high quality products
Pfizer, We are one
PGS - Manufacture the Future
Career Progression Program (CCP) for Advanced Biopharmaceuticals Manufacturing Executives/Professionals
We are pleased to announce the Career Progression Program (CCP) for Advanced Biopharmaceuticals Manufacturing Executives/Professionals, a talent development initiative aimed at cultivating the next generation of skilled professionals for Singapore's biopharmaceutical manufacturing industry.
Program Overview:
This program is designed to equip participants with skills and experience to meet the sector's hiring demand.
We invite eligible candidates to apply for this opportunity to advance their careers with Pfizer.
Why Patients Need You
Our daily work focuses on delivering safe, effective products. Our culture emphasizes quality, innovation, and customer focus. Your role impacts patients directly through development, compliance, or research activities.
What You Will Achieve
The QA Specialist will support GMP compliance, oversee GMP operations, collaborate on quality system improvements, and support regulatory readiness and inspections.
Responsibilities:
Review and approve batch records, QC worksheets, cleaning records, and GMP documentation. Support production activities, monitor processes, and ensure compliance. Act as label administrator, write deviations, and support audits and regulatory queries. Maintain inspection readiness and support continuous quality improvements.
Organizational Relationships:
Interact with manufacturing, quality control, warehouse, engineering, and regulatory teams to ensure GMP compliance and quality standards.
Qualifications:
Bachelor's in Science or Chemical Engineering; or Diploma with 5+ years QA experience. Fresh graduates considered.
Pfizer is an equal opportunity employer and complies with all applicable legislation.