Associate Regulatory Affairs Specialist (Madrid)

Associate Regulatory Affairs Specialist (Madrid)

02 oct
|
Medtronic
|
Madrid

02 oct

Medtronic

Madrid

Careers that change lives start here. Medtronic is a general leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.
A Day in the Life
About the Operating Unit / Portfolio / Function
The Regulatory Affairs function supports the registration, maintenance, and regulatory compliance of medical devices across multiple Medtronic business units in Spain. The team works closely with commercial, marketing, quality, supply chain, and tender management teams to ensure product information is accurately maintained and regulatory requirements are met throughout the product lifecycle.

About the Position
This Temporary position is based in Spain and follows a Flex work model with an expectation of regular office presence.



The role requires collaboration with local and international stakeholders and supports interactions with the Spanish Agency of Medicines and Medical Devices (AEMPS). Travel is not expected to be a significant component of the role. The Associate Regulatory Affairs Specialist supports regulatory activities related to medical device registrations, product database maintenance, and compliance processes across multiple business units. This role provides exposure to both pre-market and post-market regulatory activities and offers the opportunity to work with cross-functional teams while developing expertise in Spanish and European medical device regulations.
Primary Responsibilities
- Support the registration of new medical devices and updates to existing product registrations within the AEMPS system.
- Maintain and ensure accuracy of regulatory and product information within internal databases.
- Monitor regulatory submiss

📌 Associate Regulatory Affairs Specialist (Madrid)
🏢 Medtronic
📍 Madrid

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