Medtronic
Healthcare Technology
RegulatoryAffairsSpecialist
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Regulatory Affairs Specialist at Medtronic. Skills: Regulatory affairs, Regulatory submissions, Compliance. Prepare regulatory submissions. Publish regulatory submissions”
Industry & Context.
Troubleshooting
Minimum 4 days a week onsite
What They're Looking For.
Must Have
Baccalaureate degree, 2 years of relevant experience
Nice to Have
Experience with regulatory data systems, Experience preparing regulatory submissions, Attention to detail, Organizational skills, Ability to manage multiple projects, Ability to meet deadlines, Effective written communication skills, Effective verbal communication skills
What You'll Do.
Prepare regulatory submissions
Publish regulatory submissions
Perform quality control on submissions
Deliver regulatory submissions
Produce submissions using electronic publishing tools
Manage enterprise-wide regulatory management systems
Coordinate regulatory systems
Support regulatory system users
Maintain regulatory system data
Develop training for colleagues
Deliver training for colleagues
Contribute to regulatory systems development
Contribute to regulatory systems implementation
Contribute to regulatory systems improvement
Provide input to system design
Provide input to system enhancements
Prepare paper submissions
Prepare electronic submissions
Submit annual reports
Submit general correspondence
Submit adverse event reports
Submit promotional material filings
Archive paper submissions
Archive electronic submissions
Collaborate cross-functionally
Collect required information
Provide regulatory status updates
Report out to leadership
How You'll Work.
Team & Collaboration
Cross-functional teams; Diverse stakeholder groups; R&D; Quality; Clinical; Marketing
Communication Scope
Report-outs to leadership
Process & Methodology
Project delivery
Full Job Description
We anticipate the application window for this opening will close on - 20 Jun 2026 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** Across our global Neuroscience organization, we advance care for some of medicine’s most complex neurological and spinal conditions. By combining innovative technology, data-driven insights, and deep clinical expertise, we partner with physicians and health systems to improve how patients are treated and supported throughout their care journey. Our Cranial & Spinal Technologies (CST) Operating Unit develops and delivers an integrated ecosystem of spinal implants, navigation and robotic guidance systems, advanced imaging, and data-driven planning tools for complex spine and cranial procedures. Platforms such as AiBLE™ connect these technologies to enhance surgical precision, streamline workflows, and support improved patient outcomes worldwide. Check us out on LinkedIn: [Medtronic CST](https://www.linkedin.com/company/medtronic-brain-and-spine-therapies/posts/?feedView=all) The Regulatory Affairs Specialist is an individual contributor role within the Cranial & Spinal Technologies Operating Unit, responsible for planning and delivering regulatory projects that support timely market access and ongoing compliance. This position works cross‑functionally to prepare, publish, and manage high‑quality regulatory submissions and related documentation, leveraging specialized knowledge of regulatory requirements and electronic document systems. The role may mentor colleagues or provide direction to lower‑level professionals while ensuring work is delivered in alignment with Medtronic policies, procedures, and quality standards. At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we
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