Geylang - Regulatory Affairs Specialist [Medical Device / Up to 4,000]
Regulatory Affairs Specialist with global Medical Device MNC
- Opportunity to work on local and regional submissions
Partnering with a global Medical Device MNC with an established branding, our client is seeking a Regulatory Affairs Specialist.
Reporting to the RA Director, we are looking for someone with good knowledge of regulatory framework.
In this role, you shall assist in the execution of the regulatory strategies in assigned markets throughout the company product life cycle, with a focus on efficient pre-market and post- market regulatory approvals.
You will also support the review and approval of:
- Change control activities
- Product promotional activities
- Product registration
- Product labeling
- Regulatory inspections and audits
You should have at least 1 year of regulatory experience in medical devices and a related science degree.
For more information, please apply with your updated CV (in Word document).
Ambrose ChanRegistration Number: R1218177
EA License Number: 17C8502