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At Medtronic, you can begin a lifelong career of exploration and innovation, helping champion healthcare access and equity for all.

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.

Responsibilities

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

- Assess and determine the impact of Regulatory Assessment Changes, providing guidance and recommendations when applicable
- Follow up with Operating Units and RAC originators to clarify change information and ensure accurate interpretation of regulatory impacts
- Coordinate and support regulatory projects, tracking milestones, priorities, and deliverables to ensure timely completion of assignments
- Analyze and interpret regulatory and operational data to support decision‑making and identify trends, risks, or opportunities for improvement
- Utilize and manage regulatory and data management systems to monitor activities, maintain records, and ensure data accuracy and traceability
- Identify opportunities for process improvements, including the development or support of automation initiatives and system enhancements that improve regulatory operational efficiency




- Work independently and collaborate with other Regulatory Operations Specialists and cross‑functional partners to support project execution
- Contribute to regulatory efficiency by supporting the implementation of regulatory strategies and recommending improvements to systems and processes within the RA function
- Track, monitor, and maintain records of daily activities, project progress, and metrics in the assigned regulatory tools
- Provide guidance and support to entry‑level team members when needed, helping ensure consistency and quality in regulatory assessments

Required Knowledge and Experience

- Bachelor’s degree in the medical field
- 2 or 3 years of experience in regulatory affairs, regulatory operations, project coordination, data analysis, or a related field
- Demonstrated ability to work independently on moderately complex assignments and manage multiple priorities
- Experience analyzing and interpreting data to support operational or regulatory decision‑making
- Familiarity with data management systems, reporting tools, or platforms used for tracking regulatory or operational activities
- Interest or experience in process optimization, digital tools, or automation initiatives that improve efficiency and data management
- Fluent English

Benefits & Compensation

Medtronic offers a competitive salary and adaptable benefits package. This position is eligible for a short‑term incentive called the Medtronic Incentive Plan (MIP).

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📌 Regulatory Affairs Specialist (Bogotá)
🏢 Medtronic
📍 Bogotá