Regulatory Affairs Professional

4 days ago


Taguig, National Capital Region, Philippines Medtronic Full time

Medtronic is a mission-driven leader in medical technology and solutions. We are committed to alleviating pain, restoring health, and extending life.

We have an exciting opportunity for a Regulatory Affairs Specialist to join our team in the Regulatory Affairs department.

About the Role

This role will be responsible for executing submission strategies on-time, preparing dossiers for regulatory submissions for global regions, and liaising with operating unit regulatory affairs and stakeholders to ensure alignment on submission plans.

  • Ensure compliance with regulatory procedures and changes.
  • Provide timely status updates on projects under scope and all applicable regulatory activities assigned.
Required Skills and Qualifications
  • Bachelor's degree in pharmaceutical sciences, biomedical engineering, or a related field.
  • At least 1-year regulatory experience in medical devices.
  • Experience in document interpretation, queries, and workflow skills is an advantage.
  • Proficiency in Microsoft tools.
  • Excellent communication skills.
  • Ability to work as part of a team, good analytical and problem-solving skills.


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