Job Description
Post-Market Surveillance Analyst
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 Post-Market Surveillance Analyst, 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:
- Lead Technovigilance and Pharmacovigilance programs,
including adverse event reporting and compliance with local regulations.
- Manage product registrations, renewals, and regulatory submissions with INVIMA.
- Maintain regulatory databases and assess the impact of new regulations.
- Coordinate with general regulatory teams to obtain required documentation.
- Prepare and submit mandatory reports to INVIMA.
- Monitor product safety and support continuous benefit-risk evaluations.
- Promote awareness and training on the safe use of medical devices and pharmaceutical products.
Your Skills and Expertise
To set you up for success in this role from day one, Solventum requires (at a minimum) the following qualifications:
- Bachelor's degree in Pharmacy, Chemistry, Pharmaceutical Engineering
- 2-3 years of experience in Regulatory Affairs, Pharmacovigilance, Technovigilance, or Quality.
- Knowledge of Colombian post-market surveillance regulations and INVIMA requirements.
- Experience preparing r