Global Regulatory Affairs Specialist, Medical Devices

JNPMEDI Inc.; Singapore; On-site; SGD 70,000 - 90,000; Full time

Job summary

A leading medical technology company in Singapore is seeking a Regulatory Affairs Specialist to manage product submissions and regulatory filings. The ideal candidate will have over 5 years of experience in regulatory affairs within the medical device sector, strong communication skills, and the ability to work across diverse teams. The role involves collaboration with international partners to ensure successful regulatory approval. Competitive salary and growth opportunities are offered.

Qualifications

• Minimum 5 years of regulatory affairs experience in a medical device company.
• Knowledge of regulatory requirements and processes for product approval.
• Ability to manage multiple projects in a fast-paced environment.

Responsibilities

• Determine requirements for product submissions and regulatory filings.
• Provide regulatory guidance and review product design documentation.
• Collaborate with international teams for global regulatory submissions.

Skills

Regulatory affairs experience

Product lifecycle management

Risk management

Strong communication skills

Interpersonal skills

Job description

A leading medical technology company in Singapore is seeking a Regulatory Affairs Specialist to manage product submissions and regulatory filings. The ideal candidate will have over 5 years of experience in regulatory affairs within the medical device sector, strong communication skills, and the ability to work across diverse teams. The role involves collaboration with international partners to ensure successful regulatory approval. Competitive salary and growth opportunities are offered.