APAC Regulatory Affairs Specialist - Medical Devices

JAC Recruitment Pte Ltd; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A leading global medical device company in Singapore is seeking a Regulatory Affairs Specialist to coordinate product registration and market access in the APAC region. The ideal candidate has at least 2 years of experience in regulatory affairs within the medical device industry, with strong knowledge of relevant regulations. This role emphasizes proactive problem-solving, effective collaboration, and detailed oversight of post-market activities. Interested applicants are encouraged to apply.

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).
• Ability to collaborate effectively across functions and manage multiple tasks.

Responsibilities

• Coordinate product registration and market access approval in designated APAC countries.
• Provide expert advice on interpreting regulatory guidance and standards.
• Liaise with local authorities for regulatory problem-solving.
• Lead post-market surveillance activities, including complaint reporting and recall coordination.

Skills

Proactive attitude

Excellent communication skills

Problem-solving skills

Detail-oriented

Job description

A leading global medical device company in Singapore is seeking a Regulatory Affairs Specialist to coordinate product registration and market access in the APAC region. The ideal candidate has at least 2 years of experience in regulatory affairs within the medical device industry, with strong knowledge of relevant regulations. This role emphasizes proactive problem-solving, effective collaboration, and detailed oversight of post-market activities. Interested applicants are encouraged to apply.