Global Surgery Gs Reg Affairs Support Associate

J&J FAMILY OF COMPANIES

Taguig, National Capital Region, Philippines
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International market regulatory requirements
Regulatory document preparation and submission
Cross-functional stakeholder coordination
** Johnson & Johnson is seeking a Global Surgery Regulatory Affairs Support Associate to join their Global Services team in Taguig, Philippines. The role involves supporting regulatory activities for the Global Surgery MedTech portfolio by gathering regulatory requirements, preparing documents, and ensuring compliance with international standards. **

Job Summary

  • This role supports the Global Surgery MedTech Regulatory Affairs team, specifically focusing on Reconstructive and Aesthetics business units.
  • The position requires gathering international market regulatory requirements and preparing response packages to support submissions across multiple countries.
  • Candidates will work within a diverse network of professionals in over 60 countries to drive innovation and improve customer experience.

Matching Summary

Match Score: 75

** Johnson & Johnson is seeking a Global Surgery Regulatory Affairs Support Associate to join their Global Services team in Taguig, Philippines. The role involves supporting regulatory activities for the Global Surgery MedTech portfolio by gathering regulatory requirements, preparing documents, and ensuring compliance with international standards. **

Skills & Requirements

Must-have

  • International market regulatory requirements
  • Regulatory document preparation and submission
  • Cross-functional stakeholder coordination
  • English communication skills
  • Version control and documentation management
  • Process improvement and workflow optimization

Nice-to-have

  • Multinational corporation experience
  • Additional language capability
  • Critical thinking and problem-solving mindset
  • Digital environment proficiency
  • Team-oriented leadership mindset

Key Requirements

  • Bachelor's degree required
  • 3+ years professional experience in medical device or healthcare
  • Experience in Regulatory, Quality, or Clinical fields
  • Ability to work effectively in cross-functional environments

Work Rights

Not specified

Tailored Resume

Cover Letter