About this role
Senior RAQA Specialist at Terumo. Location: Selangor or Malaysia or Singapore or Myanmar or Sri Lanka or Bangladesh or Cambodia or Lao People"s Democratic Republic or Brunei Darussalam or Nepal or Maldives or Bhutan or Timor-Leste. Role: maintaining registration, managing submissions, supporting audits Requirements: Manage medical device registrations and regulatory submissions across Malaysia, Singapore, and emerging markets; maintain QMS and GDPMD/ISO compliance; support audits, complaint handling, CAPA, and post‑market surveillance. Requires bachelor’s or diploma in pharmacy/medical science or related field and minimum 3 years RA/QA experience in medical device/pharma/healthcare. Category: Legal and Compliance Seniority: Mid Level Commitment: Full Time Workplace: Onsite Languages: English