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About the role
Key responsibilities & impact- 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 global 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
Requirements
What you’ll need- Bachelor's degree in Pharmacy, Chemistry, or Pharmaceutical Engineering
- 2-3 years of experience in Regulatory Affairs, Pharmacovigilance, Technovigilance, or Quality
- Knowledge of Colombian post-market surveillance regulations and INVIMA requirements
- Fluent in English
- Experience preparing reports for health authorities is preferred
- Strong organizational, communication, and attention-to-detail skills
- Experience as the Responsible Person registered with INVIMA for Post-Market Surveillance
- Legally authorized to work in the country of employment without sponsorship for employment visa status
Benefits
Comp & perks- Competitive pay and benefits
- Programs to support physical and financial well-being
- Equal opportunity employment