Job Title: Regulatory Affairs Specialist
Location: Singapore
About Us:
Join a leading global medical device company dedicated to advancing healthcare and improving patient outcomes worldwide. With a strong commitment to quality, innovation, and patient safety, they are expanding their reach across the dynamic Asia-Pacific markets.
Key Responsibilities:
- Coordinate product registration and market access approval in designated APAC countries.
- Provide expert advice on interpreting regulatory guidance and standards to internal and external teams.
- Liaise with local authorities for regulatory problem-solving and to obtain updated information on developing regulations.
Lead comprehensive post-market surveillance activities, including complaint reporting, analysis, FSCA, and recall coordination.
Qualifications:
At least 2 years of experience in regulatory affairs within the medical device industry.
Strong knowledge of medical device regulations and the APAC regulatory landscape (including post-market surveillance).
Proactive, detail-oriented, with excellent communication and problem-solving skills.
Ability to collaborate effectively across functions and manage multiple tasks.
Interested applicants, please click APPLY NOW.
Please note, only shortlisted candidates will be contacted.
Peh Yong Sin
JAC Recruitment Pte Ltd
EA License Number: 90C3026
EA Personnel: R2197665
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