The Career Conversion Programme (CCP) (Train-and-Place with Commitment to Hire) for Advanced Biopharmaceuticals Manufacturing Executives/Professionals is a talent development programme aimed at building the next generation of skilled manpower for Singapore's Biopharmaceuticals manufacturing industry in anticipation of hiring demand.
The training programme consists of 15 months of local attachment with GSK. Due to the nature of the programme, we can only consider Singapore Citizens and Singapore Permanent Residents. Due to the nature of this traineeship programme, kindly note that training allowances are CPF exempted.
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Role Description:
Jurong Pilot Plant Laboratory Analyst will be responsible for conducting various non-GMP laboratory tests (primarily HPLC and GC), supporting GMP FTIR and extraneious matter testing, supporting laboratory housekeeping, and supporting balance checks.
Trainee to be involved in:
- Perform routine and ad hoc laboratory testing according to established procedures
- Prepare and handle samples, reagents and other materials following laboratory safety protocols
- Operate laboratory instruments and equipment, ensuring routine calibration and functional checks are performed
- Accurately record and document test results, observations, and any deviations using Enterprise LIMS (Labware, etc.)
- Analyse and interpret test data, identifying trends, patterns, and abnormalities
- Collaborate with cross-functional teams to support research projects, product development, and process improvements
- Maintain adequate housekeeping to keep a clean and organised working environment
- Monitor and maintain laboratory consumable inventory
Education / Licenses
- Bachelor's Degree / Diploma in Chemical, Pharmaceutical, Life Sciences or Bio-processing related disciplines
- Good to have at least 2 years relevant experience in an analytical laboratory
Competencies / Skills
- Experience working in a laboratory setting, conducting tests and analyses. Knowledge of laboratory techniques, equipment operation, and data analysis
- Familiarity with quality control principles, documentation practices, and regulatory compliance
- Excellent attention to detail and accuracy in recording and analysing data
- Effective problem-solving and troubleshooting skills
- Strong organizational and time management abilities
- Ability to work independently as well as collaboratively in a team environment
Where will I be based
You will be based at one of our manufacturing site in Singapore near Jurong.
Please apply via this link: https://jobs.gsk.com/en-gb/jobs/428599
