Senior / QA Executive

GlaxoSmithKline; Singapore; On-site; SGD 50,000 - 70,000; Full time

Job summary

A global biopharma company in Singapore is seeking a Quality Oversight Specialist to ensure compliance with GMP in Warehouse and Manufacturing. The ideal candidate has a degree in Life Sciences or a related field and at least 2 years of experience in a GMP-regulated environment. This role involves supporting quality documentation and participating in audits. Join us in our mission to improve health outcomes globally.

Qualifications

• At least 2 years of experience in a GMP-regulated manufacturing environment; experience in pharmaceuticals preferred.
• Practical knowledge of current Good Manufacturing Practices and quality systems.
• Comfortable working on-site and engaging directly with production teams.

Responsibilities

• Provide day-to-day quality oversight in Warehouse, QC and Manufacturing to ensure compliance with GMP.
• Support incoming material documentation review and release.
• Participate in internal auditing and inspection readiness activities.

Skills

GMP Compliance

Documentation Review

Coaching and Mentoring

Strong Communication Skills

Cross-Functional Collaboration

Education

Degree in Life Sciences, Chemistry, Engineering or related discipline

Tools

SAP

Veeva

Job description

Site Name: Singapore - Tuas

Posted Date: Nov 26 2025

You will join a committed quality team in Singapore to protect product quality and patient safety. You will provide material and operational quality oversight during manufacturing and support investigations, audits and batch documentation. We value curiosity, clear communication, and a practical, solutions-focused mindset. This role offers growth through hands‑on experience, cross‑functional collaboration, and meaningful impact aligned with our mission of uniting science, technology and talent to get ahead of disease together.

Responsibilities

• Provide day‑to‑day quality oversight in Warehouse, QC and Manufacturing to ensure compliance with GMP and site procedures.
• Support incoming material documentation review and release.
• Perform documentation review such as logbook review, batch record review, audit trail review, changeover activities, usage decisions for QC results.
• Participate in internal auditing and inspection readiness activities and support responses to audit findings.
• Coach and work closely with Warehouse, QC and Manufacturing teams to embed quality practices.
• Willingness and ability to work a 12‑hour shift pattern (day shift).

Basic Qualification

• Degree in Life Sciences, Chemistry, Engineering or a related discipline.
• At least 2 years of experience in a GMP‑regulated manufacturing environment; experience in pharmaceuticals preferred.
• Practical knowledge of current Good Manufacturing Practices and quality systems.
• Experience with SAP or Veeva systems.
• Experience supporting health authority inspections or major audits.
• Familiarity with risk assessment and quality risk management tools.
• Demonstrated ability to coach or mentor colleagues and to influence cross‑functional teams.
• Strong written and verbal communication skills in English.
• Ability to review technical documentation and perform basic investigations.
• Comfortable working on‑site and engaging directly with production teams.

To learn more about Singapore GSK and our people, please click on this link: https://www.linkedin.com/company/glaxosmithkline/life/gsksingapore

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.