Principal Regulatory Affairs Specialist (Remote - United States)

Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and help healthcare professionals perform at their best. As a Principal 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.

Requirements

• Bachelor’s Degree or higher (completed and verified prior to start)
• Ten (10) years in regulatory affairs experience in the drug and/or medical device industry
• Experience authoring regulatory submissions and technical documentation for drug and medical device products in the United States, Canada, and the European Union
• Experience authoring regulatory strategies and regulatory change assessments
• Experience revising, reviewing, and approving product labeling, including marketing claims, to ensure compliance with global regulatory requirements

Benefits

• Medical, Dental & Vision
• Health Savings Accounts
• Health Care & Dependent Care Flexible Spending Accounts
• Disability Benefits
• Life Insurance
• Voluntary Benefits
• Paid Absences and Retirement Benefits