Business Introduction

We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance.
 

Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it’s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply.
 

We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.
 

Position Summary

The Senior/ Manager, Quality Compliance is responsible for leading and managing the quality compliance function to ensure adherence to regulatory requirements, GxP standards, and QMS policies. The role drives proactive compliance strategies and continuous improvement initiatives to ensure inspections readiness including PAIs. The role ensures Quality compliance of product life cycle management, and oversight of suppliers, third parties, complaints process and periodic product reviews. The Senior/ Manager, Quality Compliance serves as a key liaison with internal and external stakeholders, including regulatory authorities, to maintain and enhance GSK's reputation for excellence in quality and compliance. The Senior/ Manager, Quality Compliance, reports to the Site Quality Director and is part of the site Quality Leadership Team (QLT).

Responsibilities:

• Serve as primary lead for regulatory inspections (PAI and routine) and audits: prepare, host, execute, and manage CAPA follow-up.

• Ensure site-wide cGxP compliance and monitor evolving regulatory requirements (e.g., FDA, EMA, MHRA, WHO), ensuring timely updates to quality systems and processes.

• Accountable for working with SLT to grow capability in understanding Regulatory changes, associated risks and identifying appropriate CAPA

• Lead internal, external and supplier/vendor audits to verify adherence to GSK standards and regulations.

• Responsible for managing site Quality governance processes and compliance activities including but not limited to Periodic product reviews, IQA/DRAs, compliance metrics, Quality Regulatory Intelligence, Stability, Supplier Quality management and Complaints oversight.  

• Drive continuous improvement of quality systems, product lifecycle management, compliance related processes.

• Ensure electronic systems and processes support compliance and sustain data integrity.

​Why You?

This role is on-site in Singapore with a hybrid working arrangement available in line with local policy. You will be part of a collaborative, values-driven team.

Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals

• Bachelor’s degree in Life Sciences – e.g. Chemistry, Pharmacy, Chemical Engineering or related discipline.
• Minimum 8 years’ experience in investigations, internal audit, compliance or closely related roles.
• Experience leading or managing internal investigations and audit programs.
• Strong stakeholder management and communication skills with senior leaders.
• Proven ability to prioritise multiple, time-sensitive matters in a fast-paced environment.
• High level of integrity, confidentiality and independent judgement.

Preferred Qualification
If you have the following characteristics, it would be a plus

• Experience working in the pharmaceutical, biotech, or healthcare industries.
• Certified Fraud Examiner, Certified Internal Auditor, or similar professional certification.
• Experience working across multiple jurisdictions or in matrixed global organisations.
• Strong data analytics skills to support monitoring and risk assessment.
• Project management experience, with the ability to lead change and implement improvements.

How to apply

If this role aligns with your experience and career goals, we would love to hear from you. Please submit your CV and a short note explaining why you are interested in this role and how you can contribute to our team. We welcome applicants from all backgrounds and encourage anyone who meets the criteria to apply.

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

We are committed to creating an inclusive workplace and providing equal opportunities for all applicants. We embrace an agile working culture across our roles, so if flexibility is important to you please discuss opportunities with our hiring team. If you need any adjustments to the recruitment process to help you demonstrate your strengths and capabilities, contact APACRecruitment.Adjustments@gsk.com. Please note this email is for adjustment requests only; for other enquiries please use our standard contact channels.

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