What You'll Be Doing:
- Writes required GMP documentations such as SOPs, protocols, reports, deviations, change controls, OOS
- Liaising with different departments to coordinate tasks and actions
- Review and approve routine laboratory results eg. environmental monitoring, endotoxin test, sterility by membrane filtration
Who We're Looking For:
- Science degree in Life sciences, biotechnology, biochemistry, microbiology or equivalent with >2 years of experience in lab in a pharma industry
Or Diploma holders with >5 years of experience in a lab in a pharma industry
- Have previous working experience in cGMP laboratory environment
- Have experience in coordinating with different teams or eager to do so
- Have experience in writing deviations
- Have hands-on experience on environmental monitoring
Plus
- Endotoxin testing
- Elisa testing
If you have what it takes, click 'Want to Visit' now and meet with us!