About this role
Our client is a global Medical device manufacturers providing healthcare regulatory consultancy across Asia. Due to their current expansion plan, they are looking for a Senior Regulatory Affairs Specialist to join their team, in hopes of developing the current high performing team. They are located in the East area. Job Responsibilities: Determine whether products are classified as medical devices and identify appropriate regulatory pathways and risk classifications Prepare and submit regulatory applications including product registrations, renewals, and change notifications to relevant authorities Follow up on submissions and address authority feedback to support successful approvals Liaise with internal teams and external stakeholders to resolve regulatory queries and support product registration activities Maintain and update regulatory databases and ensure documentation accuracy and compliance Develop and maintain SOPs and internal regulatory policies to ensure compliance with regulatory requirements Conduct regulatory intelligence research and prepare reports on regulatory updates and industry developments Monitor regulatory changes and assess potential impact on ongoing projects, providing updates to stakeholders Support sales and commercial teams by providing regulatory advice during client discussions when required Handle post-market regulatory activities such as adverse event reporting, safety corrective actions, and product recalls Perform any ad-hoc duties when required. Requirements: Min Degree in Life Sciences/ Biotechnology / Chemistry, or related discipline Min5 years of regulatory affairs experience within medical devices Strong understanding of regulatory submission processes and compliance frameworks Familiarity with ISO 13485 and GDPMDS would be advantageous. Interested candidates who wish to apply for the advertised position, please click APPLY NOW or email an updated copy of your resume/cv. We regret that only shortlisted candidate will be no…
What they're looking for
RegistrationIso AuditingRegulatory Compliancescientific discipline
About Recruitpedia Pte. Ltd.
Industry: Administrative & support services
Frequently asked questions
What does a Senior Regulatory Affairs Specialist (Medical Devices, Is0 13485) / East Area at Recruitpedia Pte. Ltd. do?
Our client is a global Medical device manufacturers providing healthcare regulatory consultancy across Asia. Due to their current expansion plan, they are looking for a Senior Regulatory Affairs Specialist to join their team, in hopes of developing the current high performing team. They are located …
What skills does this Senior Regulatory Affairs Specialist (Medical Devices, Is0 13485) / East Area role need?
Key skills for this role include Registration, Iso Auditing, Regulatory Compliance, scientific discipline.
How much does a Senior Regulatory Affairs Specialist (Medical Devices, Is0 13485) / East Area at Recruitpedia Pte. Ltd. pay?
This role lists a salary of S$5,500 – S$6,500 per month.
Is this Senior Regulatory Affairs Specialist (Medical Devices, Is0 13485) / East Area role remote, hybrid, or on-site?
The listing is based in Islandwide. Check the posting for remote or hybrid options.
How do I apply for this Senior Regulatory Affairs Specialist (Medical Devices, Is0 13485) / East Area role?
You can apply directly on Recruitpedia Pte. Ltd.'s careers page. ApplyLah can tailor your résumé and cover letter to this exact role in seconds first.
