FreshRemote.Work

Senior Regulatory Affairs Specicalist

Remote - California

Thank you for your interest in working for our Company. Recruiting the right talent is crucial to our goals. On April 1, 2024, 3M Healthcare underwent a corporate spin-off leading to the creation of a new company named Solventum. We are still in the process of updating our Careers Page and applicant documents, which currently have 3M branding. Please bear with us. In the interim, our Privacy Policy here: https://www.solventum.com/en-us/home/legal/website-privacy-statement/applicant-privacy/ continues to apply to any personal information you submit, and the 3M-branded positions listed on our Careers Page are for Solventum positions. As it was with 3M, at Solventum all qualified applicants will receive consideration for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Job Description:

Senior Regulatory Affairs Specialist (Solventum)

3M Health Care is now Solventum

At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers’ toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue.

We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. Because at Solventum, we never stop solving for you.

The Impact You’ll Make in this Role
In this Senior Regulatory Affairs position, you will have the opportunity to act as the lead for Regulatory Affairs on cross functional teams in new product development and sustaining projects for the Dental Solutions Division. The role will have a significant impact for Tier 1 country registrations in high volume markets (US, Canada, EU, etc.). The position will work with the international regulatory affairs group to ensure products are registered globally based on the business strategy.

As a Senior Regulatory Affairs Specialist, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by:

  • Conducting change impact assessments and coordinating associated activities for assigned products.

  • Supporting new product development as required.

  • Reviewing claims and promotional items with minimal oversight.

  • Supporting Clinical Strategy Development.

  • Providing regulatory review of technical …

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Job Profile

Regions

North America

Countries

United States

Restrictions

Must be legally authorized to work in country Must be legally authorized to work in country of employment without sponsorship Must be legally authorized to work in country of employment without sponsorship for employment visa status

Benefits/Perks

Competitive pay and benefits Fully remote Relocation assistance

Tasks
  • Review claims
  • Support product development
Skills

Audit Support Business Clinical Strategy Communication Compliance Data Science Healthcare IT Medical Devices Negotiation New Product Development Process Improvement Product Development Project Management Regulatory Affairs Regulatory filings Reporting Risk Management Stakeholder management Teams Technical Training

Education

Business GED High school diploma High school diploma/GED

Certifications

Project Management

Timezones

America/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9