With your combined knowledge of scientific, regulatory and business issues, you will mainly be responsible for local regulatory matters, such as planning and executing activities necessary for product registration while complying with regulatory requirements and maintaining good contact with local regulatory authority, Health Sciences Authority (HSA). You will assist in the preparation of the SS 620:2016 Good Distribution Practice for Medical Devices (SS GDPMDS) audit and certification. You will also assist in the implementation of divisional standards and post-market surveillance requirements from HSA.
Who you are
You are someone who influences your own development, pursues your interests across functions and geographies, and understands that a job title is not the final definition of who you are, but a starting point.
You should ideally possess a bachelor degree in Biomedical Science or equivalent (preferably Medical laboratory related), preferably with 3 years of working experience in a similar role. Good knowledge of HSA medical device regulations will be an added advantage. You should be organized and meticulous, have an eye for detail, possess good analytical and problem-solving skills, as well as excellent verbal and written communication skills. You should be able to work both independently as well as in a team.
Apply online with your full resume, current and expected salaries by 9 December 2018. Shortlisted candidates will be notified within 4 weeks from the application closing date.