Regulatory Specialist, Medical Devices
2 days ago
What the role is We are looking for highly motivated individuals with a strong desire to protect public health and safety to join us as Regulatory Specialists of Medical Devices. What you will be working on Screen and evaluate medical device pre/post‐marketing applications to ascertain that medical devices meet safety, quality and performance requirements within target timelines. Implementation of the medical device regulatory framework, including effective communication of the regulatory policy to industry and other stakeholders. Respond to queries, feedback and provide clarifications to educate industry stakeholders on regulatory requirements and enhance regulatory compliance. Conduct periodic environmental scanning of the medical device market to prepare for appropriate regulatory controls for novel innovative medical devices. What we are looking for Possess knowledge and experience in related scientific disciplines, e.g., Biomedical Engineering, Biomedical Sciences, Medical Technology, Pharmacy, Public Health or any related biomedical/clinical specialties. Preferably 3‐5 years of relevant experience in the medical technology industry, including medical software. Past research experience in R&D, biological sciences, bioengineering and biomedical areas will be an advantage but not essential. Good communication and interpersonal skills. Able to work independently, as well as in a team. Able to work effectively with people from different backgrounds. Shortlisted candidates would be contacted within 30 days from the closing date of the advertisement. We regret that only shortlisted candidates would be notified. About Health Sciences Authority The Health Sciences Authority (HSA) applies medical, pharmaceutical and scientific expertise through its three professional groups, Health Products Regulation, Blood Services and Applied Sciences, to protect and advance national health and safety. HSA is a multidisciplinary authority. It serves as the national regulator for health products, ensuring they are wisely regulated to meet standards of safety, quality and efficacy. As the national blood service, it is responsible for providing a safe and adequate blood supply. It also applies specialised scientific, forensic, investigative and analytical capabilities in serving the administration of justice. For more details, visit For more updates on public health and safety matters, follow us on Twitter at and LinkedIn at #J-18808-Ljbffr
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Singapore ALCOTECH PTE. LTD. Full timeA specialist regulatory company in Singapore is looking for a Regulatory Affairs Specialist. The role includes preparing medical device registration dossiers for HSA and ensuring compliance with regulations. Ideal candidates have 2–5 years of regulatory affairs experience and strong knowledge of Singapore's medical device regulations. The job offers a...
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Regulatory Affairs Specialist
3 days ago
Singapore Hunt Talent Partners Full timeRegulatory Affairs Specialist (Medical Devices)Base salary up to $4,700/month + AWS + VB We are working with a Medical Devices MNC with its HQ based in Japan. They have a strong vision to provide high quality standards and innovations. With a staff strength of over 20,000 employees in APAC and are well known for multiple therapeutic areas ranging from...
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Regulatory Specialist
2 days ago
Singapore Health Sciences Authority Full timeA government health regulatory agency is seeking motivated individuals to join as Regulatory Specialists for Medical Devices in Singapore. The role involves evaluating medical device applications for safety and quality, implementing regulatory frameworks, and educating industry stakeholders. Ideal candidates will have 3-5 years of experience in the medical...
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Singapore Hunt Talent Partners Full timeA Medical Devices MNC in Singapore seeks a Regulatory Affairs Specialist to coordinate product registrations and ensure compliance with regulations. The role requires a minimum of 2 years in Regulatory Affairs within the Medical Devices sector. You will manage regulatory documentation and engage with various stakeholders. The position is office-based and...
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Singapore JNPMEDI Inc. Full timeA leading medical technology company in Singapore is seeking a Regulatory Affairs Specialist to manage product submissions and regulatory filings. The ideal candidate will have over 5 years of experience in regulatory affairs within the medical device sector, strong communication skills, and the ability to work across diverse teams. The role involves...
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Regional Regulatory Affairs Specialist
7 days ago
Singapore HUNT TALENT PARTNERS PTE. LTD. Full timeMedical Devices MNC headquartered in Japan New regional role covering Asia Base salary up to $4,800/month + AWS + VB We are working with a Medical Devices MNC with its HQ based in Japan. They have a strong vision to provide high quality standards and innovations. With a staff strength of over 20,000 employees in APAC and are well known for multiple...
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Junior Regulatory Affairs Specialist
3 days ago
Singapore Andaman Medical Full timeWe are looking for a Regulatory Affairs Specialist with at least 1 year experience in medical devices and or any related field, who can further assist our team in Thailand in processing medical device registration, determining risk classifications of health products and monitoring trends regarding the industry regulations. - Preparing and submitting...
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Regulatory Affairs Specialist
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APAC Marketing Specialist, Medical Devices
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Singapore Sirtex Medical Limited Full timeA global healthcare company is seeking an APAC Marketing Specialist in Singapore to drive commercial success across the Asia-Pacific region. You will manage marketing initiatives, events, and analytics. The ideal candidate will have a Bachelor's degree in Marketing or Business, with 3–5 years of experience in medical device or pharmaceutical marketing....
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Medical Device QA
2 weeks ago
Singapore Adecco Full timeA recruitment agency in Singapore is seeking a Quality Assurance Professional for a 6-month contract role in the medical devices sector. The ideal candidate will have at least two years of regulatory experience and a robust understanding of quality compliance within medical or pharmaceutical environments. The position involves ensuring product compliance,...
