Job Description

Advanced MedTech is the largest medical device company in Southeast Asia. It is a global medical technology leader with a core focus in urology devices and services. Headquartered in Singapore, with operations in US, Germany, Spain, France, Italy, China, Malaysia and Japan, the Company serves millions of patients and physicians in 100 countries worldwide. Advanced MedTech makes strategic investments in disruptive medical technology companies, strengthening its portfolio of healthcare solutions for customers around the world. Advanced MedTech is a wholly-owned subsidiary of Temasek Holdings.Position DescriptionWe are looking for a motivated and independent individual who is interested to venture into the world of quality and regulatory affairs. Reporting to the QMRA Manager, you will gain an understanding of medical device regulations across the Asia Pacific region, perform compilations of product technical files and be exposed to quality audit preparation. You will also help to compile documents for new registrations and renewal of licenses for the Asia Australia market. Throughout the internship, you will get to collaborate with other departments in a global and dynamic environment.Job Responsibilities Support product registration document preparation for APAC region Support ISO13485 audits Assist in other ad-hoc projects assigned by supervisorJob Requirements Able to commit full-time Jan - Jun 2023, under credit-bearing internship/LOA Interest in medical device regulatory and quality requirements Knowledge of ISO13485:2016 requirements Basic knowledge in HSA regulation Proficient in Microsoft Office Able to work independently with excellent interpersonal skills Adaptable in a fast-paced, results-oriented work environment Able to manage multiple tasks with accuracy, attention to detail and effective time managementWe regret that only shortlisted applicants will be notified.
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