Your new company
Be part of a leading medical devices company
Your new role
- Quality system development and deployment
- Support quality planning process
- Oversees quality system processes
- Lead audit readiness
- Develop engineers career development
- Manage design and manufacturing documentation
What you'll need to succeed
- Bachelors in Science or equivalent
- 5 years of experience in ISO 13485 environment
- Experienced in GMP environment
What you'll get in return
You will be part of a leading company who values employees and have a structured career growth and development opportunities. You will also be compensated with attractive remuneration
What you need to do now
If you're keen on pursuing this exciting opportunity, please send a copy of your CV (word document) to geraldine.tay@hays.com.sg [mailto:geraldine.tay@hays.com.sg] (Registration ID No. R22105664)
EA License No.: 07C3924 #1238390