Senior QA Specialist

Pfizer Pte Ltd; Singapore; On-site; SGD 90,000 - 130,000; Full time

Job summary

Pfizer Pte Ltd in Singapore seeks a QA professional to ensure compliant manufacturing, packaging and labelling of intermediates and APIs. You will review batch records, approve deviations, and maintain quality systems with a focus on cGMPs and regulatory standards.

You will interact with cross-functional teams, mentor junior staff, and support inspections and regulatory inquiries. Experience with Veeva Vault QMS and SAP is advantageous.

Qualifications

• Diploma with 8+ years of experience or equivalent degree with 4+ years in QA.
• Strong knowledge of cGMPs and GxP regulations.
• Ability to lead quality systems and audits.

Responsibilities

• Review and approve master batch records and executed batch records for intermediates and APIs.
• Dispositions of intermediates and APIs and review of cleaning instructions.
• Review GMP documents, SOPs, protocols, reports, and change controls.
• Maintain quality tracking systems and participate in risk assessments (FMEA).
• Support regulatory submissions and regulatory inquiries; assist inspections.

Skills

Critical thinking

Problem solving

Team collaboration

Proactive

Education

Diploma

Associate degree

BA/BS

Tools

Veeva Vault QMS

SAP

Job description

Use Your Power for Purpose

Every day, Pfizer's unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting the patient first. Whether you are involved in development, maintenance, compliance, or research analysis, your contribution directly impacts patients.

What You Will Achieve

In this role, you will:

• Review and approve master batch records and executed 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 to ensure compliance with Pfizer global and local documents.
• Review and approve GMP documents, including SOPs, protocols, reports, and change controls, to ensure compliance with Pfizer global and local documents.
• Ensure compliance with quality procedures, regulatory requirements, and current Good Manufacturing Practices (cGMPs).
• Review and approve deviations in accordance with site procedures, including investigation reports, root cause analyses, corrective and preventive actions, and impact assessments conducted with subject matter experts for quality, validation, stability, and regulatory considerations. Escalate issues in accordance with Pfizer global and local documents.
• Serve as the Designated Point of Contact (DPOC) and super user for assigned site platforms supporting quality systems, such as Veeva Vault QMS and SAP, when nominated.
• Maintain quality tracking systems and metrics to proactively identify trends and atypical observations.
• Support preparation of the Annual Product Record, evaluate trends and atypical observations, and recommend improvement actions.
• Participate in process risk assessments, such as Failure Modes and Effects Analysis (FMEA), for new product introductions and process changes.
• Assess site procedures against Pfizer global and local documents, recommend actions to close identified gaps and mitigate risks, and conduct internal audits to confirm the effectiveness of internal controls.
• Maintain inspection readiness and support regulatory and customer inspections. Participate actively in GMP walkthroughs to ensure site operations and facilities remain inspection ready.
• Support the maintenance of GMP systems and processes in a validated state.
• Support regulatory submissions and respond promptly to regulatory queries.
• Uphold Pfizer's Code of Conduct and values, demonstrate actionable attributes.
• Contribute actively within the assigned Value Stream Team (VST) by reporting performance against metrics, identifying and resolving issues, escalating as appropriate, and developing and implementing effective solutions.
• Lead improvements to Quality Assurance systems, as required.
• Mentor junior members of the Quality Assurance team, including interns.
• Participate actively in safety initiatives and conduct Environment, Health and Safety (EHS) investigations, as required.

Here Is What You Need (Minimum Requirements)

• Diploma with 8+ years of relevant experience or associate's degree with 6+ years of relevant experience or BA/BS with 4+ years of relevant experiences
• Solid understanding of current Good Manufacturing Practices and relevant GxP regulations and standards
• Strong critical thinking skills
• Ability to work effectively within own team and interdepartmental teams
• Proactive approach to problem-solving

Bonus Points If You Have (Preferred Requirements)

• Experience in quality administered systems
• Strong organizational skills and attention to detail
• Experience with regulatory compliance and documentation
• Ability to mentor and review the work of other colleagues
• Experience using common AI tools, including generative technologies such as Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use

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 onPfizer Careers.

Quality Assurance and Control