Regulatory Affairs (Medical Device MNC / Office Hours)

Regulatory Affairs (Medical Device MNC / Office Hours)

• Permanent, Full-time opportunity in a Leading Medical Device MNC
• Great platform for Growth and Career Progression
• Work-life balance; 5 day work week

As a Regulatory Affairs Specialist, you will be responsible for the registrations and renewals of products in the medical device space.

Our client is a leading MNC in Medical Devices. Focusing on solutions in clinical laboratory testing, they have become one of the largest producers of instrumentation worldwide.

The Opportunity

Our client is seeking an RA Specialist to join their regulatory team. The job scope is as follows:

• Handling regulatory affairs for local and regional (APAC)
• Prepare & submit product registration documentation
• Notify and update regulatory bodies of changes to documentation
• Maintain product approvals and dealer's licences
• Maintain product registration record and product registration database
• Keep updated on current applicable regulations and standards

The Talent

• Min. relevant Diploma in Biomedical Science/Biochemistry/Biotechnology or other relevant fields
• Experience in Regulatory Affairs (Medical Devices)
• Fresh graduates with relavant internship experience are welcome to apply!

Other Details

• Location: East (accessible by public transport)
• Work Hours: 5 Day Work Week, 9am - 6pm

Next Steps

Interested applicants, please send your resume to [email protected] with your current and expected salary

All shortlisted candidates will be contacted.

Adecco is acting as an Employment Business in relation to this vacancy.

The Adecco Group is an Equal Opportunities Employer.

Reference number JN -012021-51155_161922643924287