Quality Systems

**Site Name**: Singapore - Jurong
**Posted Date**: Aug 11 2025

At GSK Singapore in our Jurong API plant, our Quality team is dedicated to ensuring excellence across manufacturing and compliance. The team spans key areas, including Quality Systems & Data, Compliance, Audit & Regulatory, Quality Technical & Validation, Operation Quality, and QC functions. Together, we drive innovation, uphold regulatory standards, and deliver high-quality APIs, fostering a culture of continuous improvement and collaboration.

**Purpose**

**Responsibilities**:

- Define, maintain, and implement quality compliance standards for the Jurong API manufacturing site.
- Ensure adherence to internal (GSK corporate) and external requirements (ICH, FDA, EMEA, PMDA etc.) on current Good Manufacturing Practices (cGMP) and Data Integrity (DI).
- Oversee product manufacturing and supply compliance with QMS requirements.
- Set up and manage the site Quality Improvement Plan (QIP) and Data Integrity Plan (DIP).
- Lead and support key quality initiatives; collaborate with cross-functional teams to identify and implement process improvements.
- Manage strategic QMS projects from central Quality for site deployment.
- Deliver quality process / system simplification and improvement initiatives within quality functions; enhance data management practices and ensure alignment with global standards
- Enhance organizational performance by managing the site training framework aligned with global standards, systems, and processes.
- Provide governance, drive trend monitoring and review, propose continuous improvement actions via e.g. Site Quality Council meetings

**Requirement**:

- Bachelor’s degree in science, engineering, or a related field
- Experience in pharmaceutical or healthcare industries.
- At least 8 years of experience in quality systems, validation, audit or data management within a regulated industry.
- Familiarity with validation processes for equipment, systems, and processes.
- Knowledge of data integrity principles and practices.
- Experience in audits and regulatory inspections.
- Ability to work effectively in a cross-functional, matrix environment.
- Strong knowledge of Good Manufacturing Practices (GMP)
- Excellent organizational and problem-solving skills.
- Proficient in data management tools and systems.
- Strong communication skills, both written and verbal.

- Work Arrangement:
This role is based on-site in Singapore, with flexibility for hybrid working arrangements as needed.

Li-GSK

**Why GSK?**

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

GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves - feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.

**Important notice to Employment businesses/ Agencies