Biopharmaceutical Quality Assurance Specialist

1 week ago

Singapore beBeeQuality Full time
Quality Assurance and Control Specialist

We're in relentless pursuit of breakthroughs that change patients' lives. Our mission is to innovate every day to make the world a healthier place.

Pfizer Global Supply proudly shoulders the responsibility of manufacturing and distributing our wide-ranging pharmaceutical products. We offer competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.

Career Progression Program (CCP)

We are pleased to announce the Career Progression Program (CCP) for Advanced Biopharmaceuticals Manufacturing Executives/Professionals, a distinguished talent development initiative aimed at cultivating the next generation of skilled professionals for Singapore's biopharmaceutical manufacturing industry.

  • Duration: 15 months

This comprehensive program is meticulously designed to provide participants with the requisite skills and experience to meet the anticipated hiring demand within the biopharmaceutical manufacturing sector.

We invite eligible candidates to apply for this exceptional opportunity to advance their careers with one of the industry's leading organizations.

The Tuas Site

The Tuas, Singapore active pharmaceutical ingredient (API) manufacturing site is a key strategic manufacturing part of the PGS Network. Many of Pfizer's important new innovative medicines are being transferred to the Site to support the overall growth and breakthrough strategy.

Whether you are managing projects, or liaising with others, your contribution in this team will help in making our work easier and faster so that we can deliver breakthroughs that change patients' lives.

Why Patients Need You

Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients.

Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.

Key Responsibilities
  • Perform Analytical Method Transfer, Analytical Method Validation and Analytical Method verification in accordance to Standard Operating Procedures (SOPs).
  • Perform Cleaning Method Development and Validation.
  • Perform the impact assessment to products based on compendial monograph changes/updates/introduction.
  • Perform and review the regulatory submission and support for queries.
  • Perform Laboratory Investigation.
  • Support to QC Method trouble shooting.
  • Ensure training records are updated and correctly filed to reflect current testing capabilities and train the colleagues in hand on training of instrument and method written.
Qualifications
  • Bachelor's Degree.
  • Demonstrated technical skills in method transfer, 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.

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

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