Regulatory Affairs Specialist (Medical Device)

A leading medical device MNC looking for a RA specialist to join their team!

Your new company
A leading medical device MNC looking for a RA specialist to join their team!

Your new role
  • Communicate with regulatory authorities as well as overseas counterparts with regards to regulatory affairs matters such as product registrations, changes in existing products and renewals
  • Ensures regulatory support throughout product life cycle including labelling and dossier modifications. Cooperates with other departments to collect information needed for recall reporting, including initial and follow-up reports
  • Support activities related to product license maintenance and resolution of relevant regulatory issues.
  • Ensure compliance of local and international market regulatory requirements (HSA, TGA, FDA, EU, others as applicable)


What you'll need to succeed
  • At least 3 years of relevant regulatory affairs experience in medical device industry
  • Min. Bachelor’s degree holder in Life Sciences
  • Relevant experiences in regulatory affairs or a similar role/function

What you'll get in return
You will be part of a leading organization who values employees and have a structured career growth with development opportunities. You will also be compensated with attractive remunerations.

What you need to do now
If you're keen on pursuing this exciting opportunity, please send a copy of your CV (word document / PDF) to vanessa.soh@hays.com.sg

Registration ID No. R1330566 EA License No.: 07C3924 Company Registration No: 200609504D #1241680

Summary

Job Type
Permanent
Industry
Healthcare & Medical
Location
Singapore
Specialism
Life Sciences
Ref:
1241680

Talk to a consultant

Talk to Vanessa Soh, the specialist consultant managing this position, located in Singapore
#27-20 UOB Plaza 2, 80 Raffles Place

Telephone: +6562234535

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