RAQA Specialist (IVD / Medical Device)

Join one of the leading medical device company today! Excellent opportunities for learning RAQA work!

Your new company
Join one of the leading medical device company today! Excellent opportunities for learning RAQA work!

Your new role
  • Perform IVD Product registration (Class A to D) with HSA in time and in accordance with the global product launch schedule and local launch plan.
  • Effective operate regulatory pathway for medical devices in SEA region (Singapore, Malaysia, Thailand, Indonesia and others)
  • Communicate and align with the global regulatory team to get support for local product registration and manage local regulatory systems and processes.
  • Manage a post-market surveillance i.e. CAPA, FSCA, Recall, and Customer complaints.
  • Prepare and respond to quality audits conducted by the global and notified body.

What you'll need to succeed
  • At least 2 years of relevant regulatory affairs experience in IVD / Medical Device industry
  • Min. Bachelor’s degree holder in Life Sciences / Pharmacy
  • 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 #1241681

Summary

Job Type
Permanent
Industry
Healthcare & Medical
Location
Singapore
Specialism
Life Sciences
Ref:
1241681

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