At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

A Day in the Life

We’re a mission-driven leader in medical technology and solutions with a legacy of integrity and innovation. Work with us to incentivize better patient care and partner across the industry to make healthcare more affordable and accessible. Be a part of a community of experts committed to ensuring quality, affordable healthcare worldwide.
This role supports the Regulatory Affairs (RA) team in managing regulatory submissions, documentation, and compliance activities for medical devices. The position works closely with RA Managers, business partners, and international teams to ensure products meet local regulatory requirements, maintain registrations, and support the lifecycle of regulatory projects across Latin America. It combines project coordination, documentation management, and cross-functional collaboration to ensure regulatory processes run smoothly and efficiently. This position will be a remote position in Bogotá.

Responsibilities may include the following and other duties may be assigned:

• Support preparation, submission, and follow-up of regulatory applications, registrations, and approvals with health authorities
• Maintain and update regulatory documentation, databases, and tracking tools for ongoing projects
• Coordinate with internal stakeholders (business units, regulatory teams, and global partners) to gather information for submissions
• Assist with regulatory compliance activities including document management, translations, and approval notifications
• Monitor regulatory processes and follow up on timelines, submissions, and requests from government agencies

Required Knowledge and Experience:

• Bachelor’s degree in biomedical engineering, pharmacy, life sciences, or related discipline
• Basic understanding of regulatory affairs processes and medical device regulations
• Strong organizational and project coordination skills
• Excellent written and verbal communication skills to interact with cross-functional teams
• Ability to manage multiple tasks, maintain documentation accuracy, and work with regulatory databases or tracking tools
• Fluent in english

 

Physical Job Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. 

 

 

Benefits & Compensation

Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create.  We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
 

 

 

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

About Medtronic

We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people. 
We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.

Learn more about our business, mission, and our commitment to diversity here