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 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:
- Providing medical product regulatory support for Colombia inlcuding:
- Managing medical product licenses in Colombia with INVISA
- Reviewing and approving of medical product labeling, claims and advertisements to ensure alignment with country regulations and INVIMA guidances
- Requesting and managing product technical and legal documents from international and regional counterparts as needed for new product registrations or maintenance of current registrations in country
- Compiling, preparing, and submitting of dossiers for new product registrations/licenses or already established registrations/licenses
- Providing formal and informal assessments of the regulatory pathway for new product introductions or any product changes
- Following business Standard Operating Procedures (SOP’s) regarding specific regulatory activities and tracking with the consultants and distributors
Your Skills and Expertise
To set you up for success in this ro
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