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