Experience in medical device regulatory environment
Prior exposure to multinational or matrix organisations
Knowledge of customs and importation regulations (nice-to-have)
Experience engaging with regulatory authorities and cross-functional teams
Desired Characteristics
Demonstrated ability to analyze and resolve problems.
Ability to document, plan, market, and execute programs.
Ability to work independently in fast-paced environment with little supervision.
Ability to adapt to constant change and influence positive change effectively.
Team-oriented and responsive to customer needs.
Attention to Detail and Results-Oriented.
Ability to understand technical documentation and execute associated procedures
Ability to learn regulations effectively
Applies several sets of requirements together balancing strategy effectively
Inclusion and Diversity
We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership - always with unyielding integrity.
Additional Information
Relocation Assistance Provided: No
Benefits
Health insuranceVision insurance
Additional Information
Job Description Summary
Provides regulatory strategy and guidance to the Thailand business on healthcare regulatory requirements, including product launches, pre market submissions and registrations, and post market compliance. Liaises closely with global healthcare regulatory authorities. Demonstrates a strong understanding of key business drivers and applies this knowledge to effectively deliver responsibilities. Possesses a thorough understanding of how the team's work integrates with cross functional teams and contributes to overall organizational objectives.
GE Healthcare is a leading global medical technology and digital solutions innovator. Our mission is to improve lives in the moments that matter. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.
Job Description
Roles and Responsibilities
Manage end-to-end regulatory submissions and product registrations with Thailand regulatory authorities (e.g., Thailand Food and Drug Administration)
Develop and implement regulatory strategies aligned with business objectives and product launch timelines
Ensure compliance with pre-market and post-market regulatory requirements, including reporting and documentation updates
Interpret and apply country-specific regulatory requirements, assessing impact on submissions and approvals
Support regulatory inspections, audits, and compliance activities
Assess adverse events and field actions and ensure timely regulatory reporting
Collaborate with global regulatory, business, marketing, and logistics teams to ensure alignment on submissions, product registration timelines, and regulatory requirements
Manage regulatory and customs-related inquiries/issues to ensure smooth business operations
Provide updates and present regulatory progress, timelines, and risks to leadership
Qualifications / Requirements
Bachelor's degree in Science, Pharmacy, Biomedical Engineering, or related Engineering discipline
3-8 years of experience in Regulatory Affairs within medical devices industry
Strong knowledge of Thailand regulatory requirements and submission processes
Familiarity with Quality Management Systems (QMS)
Fluent in Thai language (mandatory) and strong English communication skills
Proven ability to work independently in a fast-paced environment
Strong analytical, problem-solving, and stakeholder management skills
Gehc · Bangkok, Thailand