Regulatory Affairs Manager (Medical Device)

Regulatory Affairs Manager in a leading Medical Technology and Devices Company

Your new company
Join one of the leading medical technology company today. They use innovative capabilities in technology and precision manufacturing to enhance the quality of life for patients. Company located in the Central region.

Your new role
  • Evaluate regulatory risks of Medical Business division
  • Develop new regulatory policies, processes and SOPs
  • Responsible for product submissions license renewals, registrations with domestic and international regulatory agencies
  • Oversee processes involved with maintaining annual licenses, registrations, listings and import/export controls Review and approve advertising and promotional items to ensure regulatory compliance
  • Provide regulatory input for product recalls and recall communications
  • Manage team of regulatory professionals and provide guidance on regulatory strategies

What you'll need to succeed
  • At least 5 years of relevant regulatory affairs experience in medical device industry
  • ASEAN exposure will be advantageous
  • Good knowledge of medical device regulatory submissions (510(k) or PMA)

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 []

Registration ID No. R1330566
EA License No.: 07C3924 #1233258


Job Type
Scientific and R&D
Life Sciences

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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