Senior Regulatory Affairs Specialist (Remote – United States)
Remote - Texas, United States
Job Description:
Senior Regulatory Affairs Specialist (Remote – United States)
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
As a Senior Regulatory Affairs Specialist, you will lead a regulatory affairs team supporting the Negative Pressure Wound Technology portfolio – a functional area that is a strategic growth driver for Solventum and has corporate-wide impact. This role will support teams in early and late-stage product development to advance the product through critical milestones and regulatory activities that lead to product approvals, globally. In addition, this role will support on-going product compliance throughout the device’s lifecycle. You will actively build strong relationships across stakeholders, management, and with contract organizations. You will be responsible for developing a team that has the appropriate capacity and competence to support the strategic plans of the business
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 …
This job isn't fresh anymore!
Search Fresh JobsJob Profile
Must be legally authorized to work Must be legally authorized to work in country Must be legally authorized to work in country of employment 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 Must be located in the United States
Benefits/PerksCollaborative environment Competitive pay Competitive pay and benefits Dental Disability benefits Flexible Spending Accounts Health Savings Accounts Innovative Culture Life Insurance Medical Paid absences Relocation assistance Remote-first company Remote work Retirement benefits Vision
Tasks- Develop regulatory strategies
- Lead regulatory affairs team
- Training
Audit Branding Business Communications Compliance Corporate policies Cross-functional Collaboration Cybersecurity Data Data Science Data Tracking Decision making Documentation Engineering Healthcare ISO 13485 IT Materials Medical device Medical Device Regulations Medical Devices Organization Product Development Regulatory Affairs Regulatory Compliance Security Software Engineering Stakeholder management Strategic growth Strategic planning Teams Technical Training Wound care
Experience5 years
EducationAdvanced degree Bachelor's Business GED Higher High school diploma High school diploma/GED Master's
TimezonesAmerica/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