QA Specialist (Compliance) (PCP) 15 months training programme

Pfizer, S.A. de C.V; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

Pfizer is initiating a 15-month program to develop skilled professionals in the biopharmaceutical sector, seeking a QA Specialist to ensure compliance with GMP standards. The successful candidate will support quality assurance efforts, manage vendor quality, and contribute to a proactive quality culture within the team. Candidates should possess a degree in a related science field and have at least one year of relevant experience.

Benefits

Competitive compensation and benefits programs

Qualifications

• Strong communication skills.
• At least 1 year in the pharmaceutical industry.
• Ability to resolve issues independently.

Responsibilities

• Promote GMP compliant behaviors and quality culture at the site.
• Review and approve GMP documentation for compliance.
• Maintain inspection readiness and support regulatory inspections.

Skills

Communication

Team-oriented attitude

Problem-solving

Education

Degree in Chemistry, Microbiology, Engineering, or related Science field

Job description

QA Specialist (Compliance) (PCP) 15 months training programme

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

Job Description

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:

• Duration: 15 months
• Attachment: Local attachment to Pfizer Inc.
• Singapore Citizens or Singapore Permanent Residents
• Have no prior working experience in the biopharmaceutical sector
• Mid-career candidates: Graduated at least 2 years prior to application

This program is designed to equip participants with the skills and experience needed to meet the sector's hiring demand.

We invite eligible candidates to apply for this opportunity to advance their careers with Pfizer.

The Tuas, Singapore active pharmaceutical ingredient (API) manufacturing site

This site is a key part of the PGS Network, supporting Pfizer’s growth and innovation strategies.

Position Summary

The incumbent is a member of the Quality Assurance team, reporting to the Senior Compliance Manager. Responsibilities include:

• Promote GMP compliant behaviors and quality culture at the site.
• Ensure compliance to Pfizer Quality Standards (PQS) and ICH guidelines.
• Oversee vendor quality management to ensure materials meet PQS.
• Work with GCMC on product filings and regulatory queries.
• Manage logistics for GMP inspections and ensure inspection readiness.
• Collaborate on quality system improvements.
• Support site in achieving high-quality manufacturing standards.

Responsibilities

• Review and approve GMP documentation for compliance.
• Qualify and manage vendors, analyze quality issues, and recommend improvements.
• Conduct internal and external audits, manage inspection logistics.
• Maintain inspection readiness and support regulatory inspections.
• Assist in regulatory submissions and responses.
• Perform gap analyses and implement improvements.
• Track quality metrics and trends.
• Participate in Quality Review meetings.
• Uphold Pfizer’s values and code of conduct.
• Contribute to Tier process improvements and safety initiatives.

Job Requirements

• Ability to resolve issues independently and escalate appropriately.
• Strong communication skills.
• Team-oriented attitude.
• Proactive and committed to success.
• Embrace digital technology for efficiency.

Organizational Relationships

Interact with various departments including Manufacturing, Quality Control, Supply Chain, Engineering, and Regulatory teams, as well as external vendors and regulatory bodies.

Education

Degree in Chemistry, Microbiology, Engineering, or related Science field.

Experience

At least 1 year in the pharmaceutical industry; strong communication skills.

Pfizer is an equal opportunity employer.