Career Conversion Programme – MSAT Manufacturing Support Engineer

Overview

Site Name: Singapore - Tuas

Posted Date: Sep 8 2025

Help us get ahead of disease together with our Vaccines manufacturing.

Education required: BS or higher degree in Chemical Engineering, Mechanical Engineering, Manufacturing Engineering, Biotechnology, or related Life Science.

Other requirements: Demonstrated skill and knowledge with analytical methods, equipment, process, software, cleaning, and facility/utility validation strategies and policy, protocol and report writing and execution.

Language requirement: Written and spoken fluency in English.

Start date: ASAP

Application deadline: We will close this vacancy when we have enough applications, so please apply as soon as you can so your application can be considered.

The MSAT Manufacturing Support team provides technical expertise to drive commercial manufacturing process improvements and support validation strategies in accordance with cGMP requirements. The role includes deviation investigations, process and equipment troubleshooting, CAPA management, change management of equipment/process/Incoming Materials, QMS gap analysis, risk assessment of technical topics, leading continuous improvement projects, and process optimization. You will validate/qualify systems used to develop and manufacture products within the manufacturing facility and ensure operations run to specifications and regulatory standards.

Direct coordination with other MPUs for knowledge sharing and supporting MSAT Product Stewardship and MSAT Technology Transfer teams in managing operational projects are also part of the role.

There is a 15-month local attachment with GSK as part of the Career Conversion Programme (CCP) for Advanced Biopharmaceuticals Manufacturing Executives/Professionals. Due to the programme, only Singapore Citizens and Singapore Permanent Residents will be considered. A certificate is awarded upon completion.

• Manufacturing operations, including management of technical deviations and CAPAs, investigations and troubleshooting of process and equipment issues
• Continuous improvement methods
• Audit preparation and management
• Project management
• Validations
• Environment, safety, health and wellness

• At least 3 years of experience in Engineering, pharmaceutical industry, or equivalent education preferred
• Familiarity with global validation/qualification requirements
• Good troubleshooting skills
• Knowledge of equipment used in vaccines manufacturing processes
• Experience with quality and process improvement methodologies and tools (Lean, Six Sigma, value stream mapping, FMEAs, DMAIC) is desired
• Lean/Sigma or Green Belt certification is a plus
• Strong communication, facilitation, negotiation, and teamwork skills
• Excellent interpersonal, written, and verbal communication
• Adaptability to a fast-paced, dynamic environment with shifting demand
• Continuous improvement mindset

• Understand and experience the GSK culture
• Work with a diversified team of professionals
• Apply and develop technical knowledge and skills
• Develop soft skills such as interpersonal, communications and negotiation skills
• Transport to and from site to MRT stations in centralized locations across Singapore (manufacturing sites)

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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 billions by the end of the decade, focusing on four therapeutic areas to impact health at scale.

GSK is committed to an environment where our people can thrive and focus on what matters most, guided by a culture of being ambitious for patients, accountable for impact and doing the right thing.

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