Regulatory Affairs Director

22 hours ago


Singapore Solventum Full time

**3M Health Care is now Solventum**

At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers’ toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue.

We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. Because at Solventum, we never stop solving for you.

**The Impact You’ll Make in this Role**
As the Regulatory Affairs Director, you will lead the APAC Regulatory Affairs team - a functional area that is strategic and has corporate-wide impact. This role will serve as a primary point of contact for the APAC team members and as a key contributor to governance decisions for strategic alignment and direction for the area. You will actively build strong relationships across stakeholders, management, and with contract organizations. You will be responsible for developing a team that has the appropriate capacity and competence to support the strategic plans of the business.

As the Regulatory Affairs Director, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by:

- Developing and executing regulatory strategies to achieve product approvals faster than competitors.
- Directing complex decision making among stakeholders and senior leaders in an area of regulatory that is complex and evolving.
- Advising and guiding the regulatory strategy development, Health Authority interactions, and submission activities to support the Med-Surg and Dental Solutions product portfolios.
- Collaborate with internal teams, including R&D, Quality Assurance, and Clinical Affairs, to ensure regulatory requirements are integrated into product development and lifecycle management processes.
- Participate in global business and functional strategic leadership meetings and forums representing regulatory affairs perspective while supporting the Med-Surg and Dental Solutions business.
- Mentoring and guiding regulatory staff and teams working across all product modalities.
- Establishing goals and objectives.

**Your Skills and Expertise**

To set you up for success in this role from day one, Solventum requires (at a minimum) the following qualifications:

- Bachelor's degree or higher in a Science or Engineering discipline
- Ten (10) or more years of Regulatory Affairs experience in the medical device industry.

In addition to the above requirements, the following are also required:

- Master’s degree in a Science or Engineering discipline
- Previous Medical Device / Healthcare experience
- Ability to manage, direct, and develop a team located in multiple countries, including China and Japan
- Excellent verbal and written communication skills in English
- Deep regulatory experience across multiple APAC countries
- Detail oriented with the ability to navigate matrix environment

**Work location**:Remote - must reside in an APAC country

**Travel**:May include up to 25% domestic/international

**Relocation Assistance**:Is not authorized

**Must be legally authorized to work in the country of employment without sponsorship for employment visa status (e.g., H1B status).**

**Supporting Your Well-being**

Solventum offers many programs to help you live your best life - both physically and financially. To ensure competitive pay and benefits, Solventum regularly benchmarks with other companies that are comparable in size and scope.

Solventum is committed to maintaining the highest standards of integrity and professionalism in our recruitment process. Applicants must remain alert to fraudulent job postings and recruitment schemes that falsely claim to represent Solventum and seek to exploit job seekers.

**Solventum Global Terms of Use and Privacy Statement**

terms.



  • Singapore PharmEng Technology Full time

    **Regulatory Affairs Director** Join a leading global organization as a **Regulatory Affairs Director**, shaping regulatory strategies across multiple regions. This high-impact role ensures compliance, drives regulatory approvals, and collaborates with senior leadership and health authorities worldwide. **Key Responsibilities**: Develop and implement...


  • Singapore Barrington James Full time

    Director of Regulatory Affairs and QualityDirector of Regulatory Affairs and QualityDirect message the job poster from Barrington JamesHead of Regulatory Affairs & Quality, Asia.I am engaged by a global medical devices company to appoint a Head of Regulatory Affairs and Quality for Asia.This senior leadership position will guide regulatory direction and...


  • Singapore Kimberly-Clark Full time

    The** **Director, Regulatory Affairs - APAC K-C Professional (KCP) & Consumer** **leads the regional regulatory affairs team for APAC (Asia-Pacific, Australia & China), and is responsible for establishing, implementing and maintaining required regulatory compliance for the business. The APAC Regulatory Affairs team provides strategic regulatory compliance...


  • Singapore INTEGRITY PARTNERS PTE. LTD. Full time

    As a **Regulatory Affairs Director **, you have the opportunity to make a significant impact on the organization and its stakeholders. By navigating the regulatory landscape, developing strategies, and effectively leading cross-functional teams, you inspire collaboration, innovation, and a shared sense of purpose. Your role as a Regulatory Affairs Director...


  • Singapore ABIORES PTE. LTD. Full time

    Develop and implement regulatory strategies to secure product approvals more quickly than competitors. - Lead complex decision-making processes among stakeholders and senior leadership in a dynamic regulatory environment. - Provide expert advice on regulatory strategy, Health Authority engagement, and submission activities for the IVD product lines. -...


  • Singapore Satcom Direct Full time

    Gogo Business Aviation is looking for a **Regulatory Affairs Director** to obtain regulatory approvals globally, with a primary focus on the Asia Pacific region, for operation of Gogo’s global broadband inflight connectivity system to enable Wi-Fi and GEO and LEO satellite connectivity onboard business airlines. You will develop and manage partnerships...


  • Singapore NOVO NORDISK PHARMA (SINGAPORE) PTE LTD Full time

    **About the department** You will join our Regulatory Affairs team in Region APAC, based in Singapore. Our team is responsible for ensuring regulatory compliance for new products and product amendments, thereby keeping our license to operate. We work closely with health authorities and policymakers to shape future regulatory frameworks and ensure the safety...


  • Singapore DSM-Firmenich Full time

    COMPANY DESCRIPTION As innovators in nutrition, health, and beauty, dsm-firmenich reinvents, manufactures, and combines vital nutrients, flavors, and fragrances for the world’s growing population to thrive. With our comprehensive range of solutions, with natural and renewable ingredients and renowned science and technology capabilities, we work to create...


  • Singapore LABGISTICS ASIA PTE. LTD. Full time

    **Responsibilities**: - Lead and supervise the SG Regulatory Affairs (RA) - Accountable for all Products Registration, renewals, and amendments - Communicate with regulatory authorities as well as regional RA team regarding regulatory affairs matters such as product registrations, changes in existing products and renewals. - Advise internal stakeholders on...


  • Singapore Johnson & Johnson Full time

    The Regulatory Affairs Specialist (MD) is a member of the local Regulatory Affairs department, responsible for activities to support and actively contributing to the regulatory compliance of medical devices products under their responsibility. - The Regulatory Affairs Specialist (MD) will be a member of the local regulatory affairs department within Johnson...