Process Engineer at GSK

Singapore, , Singapore -

Full Time

Start Date

Immediate

Expiry Date

05 Aug, 26

Salary

0.0

Posted On

07 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Process Engineering, Troubleshooting, Root Cause Analysis, Commissioning, Qualification, Validation, cGMP, Hazard Assessment, Process Risk Assessment, SOP Preparation, Scale-up, Tech Transfer, Continuous Manufacturing, Process Analytical Technology, Process Modeling, Biopharma Synthesis

Industry

Pharmaceutical Manufacturing

Description

Site Name: Singapore - Jurong Posted Date: May 7 2026 Business Introduction At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together. Find out more: Our approach to R&D Position Summary You will design, improve and support manufacturing processes at our Singapore site. You will work with operations, quality, engineering and safety teams to solve problems, deliver projects and improve performance. We value clear thinkers who act with care, work well with others, and seek practical solutions. This role offers strong growth, visible impact on site operations, and the chance to help GSK unite science, technology and talent to get ahead of disease together. Responsibilities This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: - Lead process engineering activities for NCE projects in the pilot plant, collaborating with Chemists, Operations, and Engineering teams to review scale-up requests and identify optimum plant configurations for efficient process transitioning. - Troubleshoot process and equipment issues to restore and improve production reliability. - Support process development and optimization to scale-up or tech transfer processes. - Define and monitor key performance indicators and drive improvement actions with stakeholders. - Support new equipment and computer system installation, commissioning, qualification and validation activities. - Contribute to facility capital projects. - Provide technical guidance and training to operators and colleagues to embed best practices. Why You? Basic Qualification We are seeking professionals with the following required skills and qualifications to help us achieve our goals: - Bachelor’s degree in Chemical, Biochemical or related engineering field. - Minimum 2 years’ experience in manufacturing or process engineering in pharmaceutical, biotech or related industry. - Practical experience with process troubleshooting and root cause analysis. - Experience supporting equipment and computer system commissioning, qualification or validation. - Knowledge of current Good Manufacturing Practice (cGMP), health and safety requirements. Conduct hazard assessments, complete Process Risk Assessments, review batch records, and prepare documentation such as Work Instructions (WIs) or Standard Operating Procedures (SOPs). - Strong communication and teamwork skills with a commitment to clear, respectful collaboration. Preferred Qualification If you have the following characteristics, it would be a plus: - 5+ years’ experience in pharmaceutical or biomanufacturing environments. - Experience with continuous manufacturing, process analytical technology or process modeling. - Knowledge of cleanroom standards and operations relevant to pharmaceutical manufacturing. - Experience with Biopharma synthesis workflows and scale-up, including familiarity with solid phase synthesis, purification techniques (e.g. IEX chromatography, TFF/UF/DF), freeze drying). - Familiarity with computerized maintenance or manufacturing systems (e.g., SAP, MES). Working arrangement This role is on-site in Singapore. You will regularly collaborate across teams and be present in the manufacturing area to support operations and projects. What we value in you We look for people who work with integrity, care for patient safety, and who listen and learn from others. You will bring practical engineering skill, curiosity for better ways of working, and a willingness to step in when needed. We support career growth through visible work and cross-functional learning. How to apply If this role matches your skills and ambitions, we encourage you to apply. Share your CV and a short note about a process improvement or troubleshooting success you led. We look forward to hearing from you. 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. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Responsibilities

Design, improve, and support manufacturing processes at the Singapore site, focusing on NCE projects in the pilot plant. Collaborate with cross-functional teams to troubleshoot equipment issues, drive performance improvements, and support equipment installation and validation.