Career Conversion Programme

Career Conversion Programme – MSAT Manufacturing Support Engineer GSK Location: Singapore – Tuas | Posted: Nov 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. Expected 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. What will you do?The Manufacturing Science & Technology (MSAT) Manufacturing Support team is an agile and fast responsive team that contributes to the MSAT department mission by driving commercial manufacturing processes improvements and providing technical expertise in various process disciplines. It also provides technical support to enable Value Streams to deliver their operational objectives optimally and in compliance with cGMP requirements. Areas of support include deviation investigations, process and equipment troubleshooting, CAPA management, change management of equipment, process and incoming materials, QMS gap analysis and risk assessment of technical topics. Lead continuous improvement projects and process optimisation. The MSAT Manufacturing Support Engineer is responsible for validating/qualifying the systems used to develop and/or manufacture products within manufacturing facility. They will ensure systems are running according to necessary specifications and operate within regulations to ensure data integrity and the production of quality products. MSAT Manufacturing Support Engineer directly implements, executes, and supports validation strategy at the GSK Tuas Site ensuring harmonisation with local, regulatory, and GSK standards. They manage, schedule, coordinate and execute assigned qualification or validation activities to ensure timely completion of the Validation Plan in coordination with Users, Technical Services, Quality Control, Quality Assurance, and Regulatory departments. What will you learn?Manufacturing Operations – manage technical deviations and CAPAs, manage investigations and troubleshooting of process and equipment issues. Continuous improvements Audit preparation and management Project management Validations Environment, safety, health and wellness What are we looking for?At least 3 years' experience in Engineering, pharmaceutical industry or equivalent education preferred. Familiar with global regulations validation/qualification requirements. Good troubleshooting skill. Knowledge in 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. Experience with product/process development and project management is a plus. Lean Sigma/Green Belt certification is a plus. Highly effective communication, facilitation, negotiation, and teamwork skills are required. Excellent interpersonal, written, and verbal communication skills. Adaptable to fast‐paced, dynamic work environment with shifting demand. Continuous improvement mindset. What do we offer you?Understanding and experience of GSK Culture. Work with a diversified team of professionals. Implement technical knowledge and skills that you have acquired at school. Apply and develop soft skills such as interpersonal, communications and negotiation skills. Transport to and from site to MRT stations in centralised locations all across Singapore (only for manufacturing sites). Learn more about the application process: Need help with your application? Please email us at 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 between the employment business or agency and GSK. In the absence of such written authorization any actions undertaken by the employment business or 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 or agencies in respect of the vacancies posted on this site. Details Seniority level: Not Applicable Employment type: Full‐time Job function: Manufacturing Industries: Pharmaceutical Manufacturing Why GSK? UNITING SCIENCE, TECHNOLOGY AND TALENT TO GET AHEAD OF DISEASE. 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. #J-18808-Ljbffr