Job Description

[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]

• Screenandevaluatemedical devicepre/post-marketing applicationsto ascertain that medicaldevices meetsafety, qualityand performancerequirements within target timelines.
• Implementation ofthe medical device regulatoryframework,includingeffective communicationofthe regulatorypolicytoindustry andotherstakeholders.
• Respondto queries,feedbackandprovideclarificationsto educateindustrystakeholderson regulatoryrequirementsand enhanceregulatory 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.