Post-Market Surveillance Analyst

About the role

Solventum is seeking a Post-Market Surveillance Analyst to support the safety and regulatory compliance of its medical devices and pharmaceutical products in Colombia. You will work in a hybrid setting, collaborating with global regulatory teams and local health authorities.

Key responsibilities

• 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, assess new regulations, and prepare mandatory reports for INVIMA.
• Coordinate with global regulatory teams to obtain required documentation and support continuous benefit‑risk evaluations.

Required profile

• 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 and legally authorized to work in Colombia without sponsorship.

Required skills

• Technovigilance and Pharmacovigilance processes.
• Regulatory submission preparation for INVIMA.
• Regulatory database management.
• Strong organizational and communication abilities.