• Maintain the validation programs for all the company divisions with products processed through Regional Sterilization • Manage the facility environmental and personnel safety program • Conduct all sterilization validation • Implements and understands FDA or regulatory requirements as necessary. • Applies technology principles to multiple tasks. Working knowledge of cross-functional and related technical areas. • Highlights risks and understands how to approach and complete tasks, avoiding serious delays and considerable expenditure of time and resources. • Advises team members pro-actively on technical ideas and promotes skill development of team work. • Interacts with peers across projects to secure resources and commitments.
Yêu cầu công việc
• Bachelor’s Degree in Engineering • Knowledge in physical, chemical, and biological sciences • Two years of GMP manufacturing experience required.
Quyền lợi được hưởng
- Attractive Package + 13th Payment + Performance Bonus - Insurance for Employee and 02 relatives - Transportation