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Full-time Healthcare & care · Posted 28 Sept
Senior/Biotechnologist (contracted till 30 Nov 2027) G GSK From company site
Salary
Not stated by the company
Start Not stated
Work mode On-site
Experience Experienced About the role This role supports the build-up of end-to-end production operations at a new manufacturing facility in Tuas, working under a Shift Supervisor. It suits people with a biotechnology, chemical engineering or life science background who are comfortable in a regulated manufacturing environment. Senior levels take on extra guidance and planning duties.
What you'll do Prepare and supply media, buffers and materials Manufacture intermediates and drug substance Help optimise use of capacity and manufacturing resources, including manpower at senior level Follow cGMP and safety requirements Meet project milestones and deliverables Take part in commissioning and qualification activities Know someone for this? Share it
Senior/Biotechnologist (contracted till 30 Nov 2027) job at GSK, Tuas | WorkJio
Support small equipment sourcing and material introduction
Collate process information for detailed design
Draft documents such as SOPs, checklists, OJT and WRA
Suggest improvements and join continuous improvement projects
Carry out other duties assigned by the supervisor
At senior level, act as in-charge by process or operations area and guide the team
Keep to the project timeline
At senior level, help the Lead Biotechnologist or Shift Supervisor with team operations planning
Complete training and qualification on current SOPs and OJT before starting operations
Discuss personal development with the supervisor and follow the agreed plan
At senior level, support new joiners, develop as a process SME, guide junior staff and conduct classroom and OJT training
Comply with IOQ, commissioning protocol, SOP and batch record requirements
Review documentation on time and make corrections
Take part in deviation investigations and CAPA implementation
Join cGMP self-inspections
Operate computer applications linked to production equipment
Record and maintain documentation correctly and in line with cGMP
Communicate clearly with the supervisor and colleagues on safety, quality and efficiency matters
Help develop and update production checklists, SOPs and validation protocols
Perform VS review of completed documentation for GDP adherence
At senior level, lead design and drafting of work instructions and SOPs
Take part in new technology and process transfers
Follow site safety procedures and work safely
Report potential safety issues
Keep assigned production areas tidy to reduce hazards
Join safety inspections and workplace risk assessments
Coordinate with colleagues on material and buffer supplies, calibration and maintenance, and QC sampling needs
Build good working relationships with QA, QC and TS Good to know Contracted until 30 Nov 2027 Based in Tuas, Singapore Reports to the Shift Supervisor Roles available across fermentation, purification, material prep and media/buffer prep areas Requirements Nitec, Higher Nitec or Diploma in Biotechnology, Chemical Engineering, Life Science or a related field Experience in biologics, chemical, pharmaceutical, food or another regulated industry is preferred Good communication skills Good documentation skills Quality mindset Disciplined Apply on the company website
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Open application Listing ID 4378 · Report this listing