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Pharmatech Associates

We are looking for a Regulatory Affairs Consultant to support several ongoing projects at about 10-20 hours per week. This role is remote. Job Duties * Work closely with Pharmatech and our client ...

Boston Scientific

Here, you'll be supported in progressing - whatever your ambitions. About the role: Boston ... As a Senior Regulatory Affairs Specialist, you will provide Regulatory Affairs support for product ...

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As of Sep 15, 2026, the average hourly pay for regulatory affairs support in the United States is $34.60, according to ZipRecruiter salary data. Most workers in this role earn between $22.36 and $26.20 per hour, depending on experience, location, and employer.

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Infographic showing various Regulatory Affairs Support job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 73% Full Time, 21% Part Time, and 5% Contract. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $71,960 per year, or $34.6 per hour.

Regulatory Affairs Specialist

Saint Paul, MN • On-site

Scanlan International
51 - 200 employees
Learn more about Scanlan Internationalexternal

Other

Posted 13 days ago

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Regulatory Affairs Specialist

Regular Full-Time Scanlan International, Inc., St. Paul, MN, US

The Regulatory Affairs Specialist will assist in maintaining market authorizations for Scanlan products, including design files, technical documentation, product registrations and listings. They will also assist with post-market surveillance and post-delivery regulatory activities necessary to ensure Scanlan products remain state-of-the-art for worldwide markets.

Position Responsibilities / Essential Functions:

Percentage Time

Accountability

30%

Market Authorization(assist with the following)

  • US FDA Registrations/Listings
  • Canada Medical Device Licenses
  • EU product registrations
  • Rest of World product registrations
  • Maintain product submissions
  • Maintain CE certification
  • Maintain CFGs
  • Maintain D of Cs
  • Maintain Product Lists

30%

  • Update design files, technical files, risk files, and other technical documentation based post-market surveillance data and trends.

30%

Post Delivery Activities(assist with the following)

  • CAPA and Complaint investigations and record keeping
  • Product return coordination for complaint investigations

10%

General Regulatory Affairs Support

  • Inquiries and sales support activities
  • Tender and quote reviews
  • Customs and import/exports support activities
  • Regulatory documentations and records management

QUALIFICATIONS:

Required Qualifications:

Education:

  • Bachelor’s degree in life sciences or other related field.

Experience:

  • 1 - 3 years of regulatory affairs work experience with medical devices.

Skills:

  • Computer proficiency in Microsoft Office applications.
  • Excellent communication skills, especially written communications.
  • Excellent organizational and record keeping skills.
  • Attention to detail with excellent proofreading, writing and editing skills.
  • Good team player with a collaborative work style.

Preferred Qualifications:

Education:

  • Master of Science – Regulatory Affairs

Experience:

  • Preparing and submitting regulatory submissions.
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