jobs in Equitable Technologies

Full Time Regulatory Affairs Associate (Medical Devices) - Graduate Program Jobs, in Equitable Technologies Federal Territory - Maukerja

Regulatory Affairs Associate (Medical Devices) - Graduate Program

KL City, Federal Territory

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Working Location

  • Kuala Lumpur Federal Territory Malaysia

Job Description

Responsibilities

Company Overview

Equitable Technologies is an MIT-founded medical technology startup headquartered in Boston, with a fast-growing product development hub in Kuala Lumpur. We’re currently operating in stealth mode as we develop a breakthrough approach to cancer screening — a mission with the potential for significant real-world impact.

We’re supported by a world-class advisory board with leaders from MIT, Harvard, the US FDA, and Cleveland Clinic. We’re now growing our team in KL to help shape and deliver this technology to the world.


About the Role

Help bring the next generation of medical technology to market.

Join our Graduate Program as a Regulatory Affairs Associate and gain hands-on exposure to the regulatory and market development aspects of medical devices.

You will work closely with our team to research regulatory requirements, understand different markets, and support activities related to bringing innovative medical technology from development towards market.


What You Will Do

  • Research medical device regulatory requirements across different markets
  • Assist with regulatory research and documentation
  • Conduct market and competitor research
  • Monitor relevant regulatory updates and requirements
  • Support research related to product registration and market entry
  • Assist with organising and maintaining regulatory information


What We’re Looking For

  • Fresh graduates in Biomedical Science, Medical Science, Biotechnology, Pharmacy, Health Sciences, or related fields
  • Strong research, analytical, and documentation skills
  • Good attention to detail
  • Interest in medical devices, healthcare, and regulatory affairs
  • Ability to work independently and collaboratively
  • Strong written and verbal communication skills


What You Can Expect

  • Exposure to real medical device regulatory processes
  • Experience researching regulatory requirements across different markets
  • Exposure to product development and market entry
  • Collaboration with technical, clinical, and product teams
  • Opportunity to develop skills in research, analysis, and regulatory strategy
  • Potential transition into a full-time role based on performance and business requirements


Start Date: Immediate

If you are interested in understanding how innovative medical technology moves from product development towards market, we would like to hear from you.


Equitable Technologies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

  • Interested candidates may apply by sending a resume and cover letter to *************

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