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

This role is an exciting opportunity to lead and manage quality systems and data processes at Jurong API Plant.The ideal candidate will bring a strong blend of technical expertise, strategic thinking, and interpersonal skills to ensure compliance with regulatory standards and drive continuous improvement initiatives. With a focus on process and system optimization, they will support the delivery of high-quality APIs while leveraging their planning and organizational abilities to manage change effectively.
Collaboration is central to this position, requiring teamwork and stakeholder engagement to align priorities and enhance quality systems. Analytical and logical thinking will be key to identifying risks and implementing robust risk management strategies. The candidate will also demonstrate exceptional influencing skills to drive consensus and support for quality initiatives.
We value candidates who are detail-oriented, proactive, and passionate about quality and data management. Their ability to balance multiple priorities with strong organizational skills will ensure the successful delivery of projects and compliance standards. This role is ideal for someone who thrives in a dynamic environment, is solution-oriented, and is committed to fostering a culture of excellence and compliance.

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.
• Support audits and inspections, acting as a subject matter expert for quality systems and data.
• Provide governance, drive trend monitoring and review, propose continuous improvement actions via e.g. Site Quality Council meetings