Global Surgery Gs Reg Affairs Support Associate

J&J FAMILY OF COMPANIES

Taguig, Philippines
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Regulatory document preparation and compliance
Cross-functional coordination and communication
International market regulatory requirements
** Johnson & Johnson is seeking a Global Surgery Regulatory Affairs Support Associate in Taguig, Philippines, to assist in regulatory documentation and compliance for the Global Surgery MedTech division. The ideal candidate should have 3+ years of experience in the medical device or healthcare industry and possess strong communication and organizational skills. **

Job Summary

  • Johnson & Johnson is committed to diversity and inclusion and provides an inclusive work environment where each person is considered as an individual.
  • This role supports the Global Surgery MedTech Regulatory Affairs team, particularly the Reconstructive and Aesthetics business, helping to improve medical care worldwide.
  • The Global Services organization delivers best-in-class, cost-effective services and compliance to Operating Companies globally, fostering innovation and continuous improvement.

Matching Summary

Match Score: 75

** Johnson & Johnson is seeking a Global Surgery Regulatory Affairs Support Associate in Taguig, Philippines, to assist in regulatory documentation and compliance for the Global Surgery MedTech division. The ideal candidate should have 3+ years of experience in the medical device or healthcare industry and possess strong communication and organizational skills. **

Skills & Requirements

Must-have

  • Regulatory document preparation and compliance
  • Cross-functional coordination and communication
  • International market regulatory requirements
  • Document management and version control
  • Use of digital collaboration tools
  • Problem-solving and critical thinking mindset

Nice-to-have

  • Leadership and team-oriented mindset
  • Experience in multinational corporations
  • Additional language capability
  • Strong learning agility
  • Attention to detail and data integrity
  • Ability to challenge status quo

Key Requirements

  • Bachelor’s degree minimum
  • 3+ years professional experience in medical device or healthcare industry
  • Experience in regulatory, quality, or clinical roles
  • Ability to work cross-functionally with multiple stakeholders
  • Strong English communication skills
  • Experience with regulatory compliance and documentation

Work Rights

Not specified

Tailored Resume

Cover Letter