
CCP6 Trainee, QC
- Tuas, Singapore
- Permanent
- Full-time
- To prioritize and perform the various testing/analysis in timely manner, in order to support the business requirements.
- Analysis of final product, in-process, stability samples according to Standard Operating Procedures and Test Methods.
- Documentation and review of results in accordance with current Good Manufacturing Practices (cGMP).
- General lab support including housekeeping, equipment maintenance, inventory of supplies, lab supplies ordering, management of glass wares, autoclaving etc.
- Prepare, maintain standards and reagents as required by GMP documents.
- Responsible to follow data integrity requirements.
- Actively contributes to operational efficiency/continuous improvement initiatives.
- Any other duties as assigned by your Manager.
- Uphold data integrity principle in accordance to Lonza policies.
- Proactively evaluate, identify and improve data integrity process
- Degree in a relevant Science field or equivalent
- Individual without prior working experience in the biopharmaceutical manufacturing industry may also apply
- Understanding of the application of mammalian cell culture for the production of biopharmaceuticals
- Understanding of cGMP regulations
- Good problem solving and anlytical skills
- Good communication and teamwork skills