Regulatory Affairs Co-Op/Intern Job at Nova Biomedical, Waltham, MA

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  • Nova Biomedical
  • Waltham, MA

Job Description

Job Description

Job Description

Nova Biomedical is hiring a Regulatory Affairs Intern for the January 2026 Co-Op Cycle (January - July 2026) in our Waltham, MA facility. The RA Intern will provide pre-market and post-market regulatory support to US FDA, Health Canada, EU, and other International Regulatory Licensing and Registration Agencies. Other responsibilities include:

  • Support Self-Certified and Notified Body Reviewed EU Documentation Preparation
  • Support International Device Licensing and Registrations
  • Support Product Development Teams for New Product Submission Requirements
  • Review Product Labeling and assist in ECO process
  • Participate in and support internal and external Quality System Audits
  • Technical Writing

Qualifications:

  • Previous Regulatory experience preferred.
  • Previous Regulatory labeling review experience preferred
  • Knowledge of ISO 13485, FDA QSR, IVDD/IVDR

Skills and Competencies:

  • Excellent technical writing skills
  • Quality System auditing experience is preferred
  • Excellent communication skills
  • Statistics and database management proficiency preferred
  • MS Office experience

Experience/Education:

  • BS Degree in Sciences or equivalent
  • MS in Regulatory Affairs preferred
  • 0-3 years IVD or Medical Device experience, specializing in Quality or Regulatory Affairs

At Nova Biomedical, we practice our core values of mutual respect, honesty, and integrity throughout the company. With a strong sense of family in the workplace, we are proud that one third of all our employees have been with us for over 10 years.

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