APAC Regulatory Strategy Lead – Medical Devices (Remote)

3mcompany; Singapore; Hybrid; SGD 180,000 - 260,000; Full time

Job summary

Solventum is seeking a Regulatory Affairs Leader for Asia to provide regional leadership and strategic direction for regulatory programs across multiple product portfolios. The role requires building strong relationships with senior partners, guiding teams across countries, and driving market access while enabling innovation.

The ideal candidate will have 10+ years in regulatory affairs for medical devices, a science or engineering degree (with a master's preferred), and proven success in APAC

Qualifications

• Bachelor's degree or higher in Science or Engineering.
• 10+ years of Regulatory Affairs experience in the medical device industry.
• Master's degree in science or engineering.
• Dental/Medical Device or Healthcare experience preferred.
• Ability to manage, direct, and develop a global team in multiple countries.
• Excellent verbal and written English communication.
• Strong regulatory experience across APAC countries.
• Detail oriented and able to navigate a complex matrix.

Responsibilities

• Develop and execute regional regulatory strategies to accelerate product approvals in Asia.
• Provide leadership to governance forums and align regional priorities.
• Mentor regulatory staff across modalities and geographies.
• Collaborate with R&D, QA, and Clinical teams to embed regulatory requirements.
• Represent regulatory affairs in leadership meetings and strategic forums.
• Lead Health Authority interactions and submission activities for Medical, Surgical and Dental portfolios.

Skills

Regulatory leadership

APAC regulatory expertise

Cross-functional collaboration

English communication

People management

Education

Bachelor's in Science/Engineering

Master's in Science/Engineering

Job description

Solventum is seeking a Regulatory Affairs Leader for Asia to provide regional leadership and strategic direction for regulatory programs across multiple product portfolios. The role requires building strong relationships with senior partners, guiding teams across countries, and driving market access while enabling innovation.

The ideal candidate will have 10+ years in regulatory affairs for medical devices, a science or engineering degree (with a master's preferred), and proven success in APAC