Pfizer

QA Specialist

Posted Yesterday

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Singapore, SGP

In-Office

Junior

Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical

We’re in relentless pursuit of breakthroughs that change patients’ lives.

The Role

Reviews and approves pharmaceutical batch records, GMP documentation, cleaning records, deviations, change controls, investigations, and quality assessments. Performs API disposition, monitors quality metrics and trends, supports annual product reviews, inspection readiness, validated systems, regulatory submissions, and continuous improvement. Requires pharmaceutical quality experience, GMP knowledge, strong communication, and teamwork.

Summary Generated by Built In

Use Your Power for Purpose
Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. Your role is crucial in maintaining this commitment and driving forward our mission to improve patient outcomes.
What You Will Achieve
In this role, you will:

Review and approve master batch records and completed batch records for the manufacture, packaging, and labelling of intermediates and active pharmaceutical ingredients (APIs), ensuring compliance with Pfizer quality standards and registered regulatory specifications.
Perform disposition of intermediates and active pharmaceutical ingredients (APIs).
Review and approve cleaning instructions and records, ensuring compliance with Pfizer Global and Local Document Standards and ICH guidelines.
Review and approve GMP documents, including SOPs, protocols, reports, and change controls, for compliance with Pfizer Global and Local Document Standards.
Ensure compliance with quality procedures, regulatory requirements, and current Good Manufacturing Practices (cGMP).
Review and approve deviations in accordance with site procedures, including investigation reports, root cause analyses, corrective and preventive actions, and quality, validation, stability, and regulatory impact assessments conducted with subject matter experts.
Maintain quality tracking systems and metrics to proactively identify trends and atypical observations.
Support preparation of Annual Product Records, evaluate trends and atypical observations, and recommend improvement actions.
Maintain inspection readiness and support regulatory and customer inspections. Participate actively in GMP walkdowns to keep site operations and facilities inspection-ready.
Support maintenance of the validated state of GMP systems and processes.
Support regulatory submissions and respond to regulatory queries promptly.

Uphold Pfizer's code of conduct and values, demonstrate Pfizer actionable attributes.
Contribute actively within the assigned Value Stream Team (VST) by reporting performance against metrics, identifying and resolving issues, and escalating concerns appropriately.
Support continuous improvement of Quality Assurance systems, as needed.
Participate actively in safety initiatives and conduct Environment, Health and Safety (EHS) investigations as required.

Here Is What You Need (Minimum Requirements)

Diploma with at least 4 years of relevant experience or BA/BS with at least 1 year of relevant experience
Experience in the pharmaceutical industry and Quality administered systems
Sound knowledge of current Good Manufacturing Practices (part of GxP)
Ability to work effectively in a team environment, both within one's own team and interdepartmental teams
Effective written and oral communication skills

Bonus Points If You Have (Preferred Requirements)

Experience at a manufacturing site.
Managing and writing deviations
Experience in production batch record review, Enterprise Resource Planning system, investigation of non-conformance, root cause analysis and change control management
Strong problem-solving skills
Ability to work independently and as part of a team
Excellent time management and multitasking abilities
Experience using common AI tools, including generative technologies such as Microsoft Copilot to support problem solving and enhance

Work Location Assignment: On Premise
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
Quality Assurance and Control

Skills Required

Diploma with at least 4 years of relevant experience, or BA/BS with at least 1 year of relevant experience
Experience in the pharmaceutical industry and quality-administered systems
Sound knowledge of current Good Manufacturing Practices (cGMP/GxP)
Ability to work effectively in team and interdepartmental environments
Effective written and oral communication skills
Experience at a manufacturing site
Experience managing and writing deviations
Experience with production batch record review, ERP systems, non-conformance investigations, root cause analysis, and change control management
Strong problem-solving skills
Ability to work independently and as part of a team
Excellent time management and multitasking abilities
Experience using common AI tools, including Microsoft Copilot

What the Team is Saying

Pfizer Compensation & Benefits Highlights

Healthcare Strength — Health coverage is described as comprehensive across medical, dental, vision, and mental‑health support, with strong plan options and provider networks. Feedback suggests these programs are a clear standout within the total rewards package.
Retirement Support — Retirement programs feature a 401(k) with company matching plus an additional company retirement contribution. Feedback suggests these elements are consistently highlighted as valuable components of overall compensation.
Leave & Time Off Breadth — Paid vacation, holidays, and sick time are often characterized as generous, with some locations offering the ability to purchase additional vacation days. Feedback suggests this breadth contributes meaningfully to work‑life balance.

Learn more about Pfizer's Compensation & Benefits →

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The Company

HQ: New York, NY

121,990 Employees

Year Founded: 1848

What We Do

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Why Work With Us

We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.