ForgeApply · Job listing
Sr Regulatory Affairs Spec - Radio Frequency
Medtronic
Tailor your resume for this Medtronic job in about a minute.
ForgeApply tailors your resume and cover letter to this exact posting, then hands you a ready-to-submit application for Medtronic's site. Free trial, no card required.
About this role
We anticipate the application window for this opening will close on - 21 Aug 2026 Careers that change lives start here. Medtronic is a global 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 The Senior Regulatory Affairs Specialist, Radio Frequency, ensures Surgical devices are compliant with global radio, wireless, and telecommunications requirements by overseeing RF regulatory submissions, performing change-management assessments, and maintaining compliance throughout the product lifecycle. The position collaborates closely with Regulatory Affairs teams, cross-functional partners, external test laboratories, certification bodies, and international regulatory representatives to align on requirements and execution. In addition, the role drives the integration of RF compliance into broader quality and regulatory systems, ensuring consistent, scalable, and proactive compliance across all programs.
The Senior Regulatory Affairs Specialist, RF, provides technical and regulatory leadership for wireless-enabled medical and non-medical devices, supporting global market access and lifecycle compliance. The role develops and executes RF regulatory strategies for new product development and sustaining programs involving technologies such as Bluetooth®, Wi-Fi, RFID, NFC, UWB, and wireless modules, while ensuring compliance with global telecommunications, wireless, and radio regulations. The specialist collaborates with R&D, Quality, Regulatory Affairs, international teams, test laboratories, and certification bodies to support product certification, regulatory submissions, change assessments, and certification maintenance activities. Responsibilities include interpreting and applying global RF requirements and standards, reviewing RF test documentation, assessing the regulatory impact of product changes, and providing guidance on wireless integration, labeling, and compliance strategies. The role also drives continuous improvement initiatives and integration of RF compliance requirements into product development, quality, and regulatory processes to ensure scalable and proactive compliance across the device lifecycle.
The ideal candidate possesses expertise in global RF, wireless, and telecommunications regulations and demonstrated experience supporting medical, non-medical devices or other highly regulated electronic products. They have hands-on experience with wireless technologies including Bluetooth/BLE, Wi-Fi, RFID, NFC, UWB, WLAN, wireless module integration, RF exposure evaluation, EMC testing, and spectrum compliance requirements, along with a strong understanding of global certification pathways and telecommunications approval processes. The candidate is skilled at interpreting complex technical standards, assessing regulatory impacts of product changes, collaborating with engineering teams on wireless system architecture, and translating technical requirements into practical compliance strategies that enable efficient global market access.
KEY RESPONSIBILITIES
• Develop and execute global RF, wireless, and telecommunications regulatory strategies to support worldwide market access and continued compliance for wireless-enabled devices. • Lead global radio certification activities, including regulatory submissions, technical documentation, certification maintenance, and interactions with telecommunications authorities, test laboratories, and certification bodies. • Provide regulatory support for new product development and lifecycle management activities involving technologies such as Bluetooth®, Wi‑Fi, RFID, NFC, UWB, and wireless modules. • Assess the regulatory impact of product, software, firmware, supplier, manufacturing, and labeling changes on global RF certifications and market access. • Interpret and apply global RF, wireless, and telecommunications regulations, standards, and certification requirements, including ANATEL, NCC, MIC, FCC, ISED, EU RED, UK Radio Equipment Regulations, and related standards. • Review RF test plans, test reports, and technical documentation to ensure compliance with applicable regulatory requirements and standards. • Provide subject matter expertise on wireless technologies, module integration strategies, RF labeling requirements, and certification pathways. • Collaborate with cross-functional teams, international regulatory partners, and external stakeholders to resolve compliance issues and support product launches. • Drive process improvements and integrate RF compliance requirements into product development, quality, and regulatory systems to support scalable and proactive compliance programs.
Must Have: Minimum Requirements
• Bachelor’s degree required
• Minimum of 4 years of relevant experience, or advanced degree with a minimum of 2 years of relevant experience.
Nice to Have
• Experience supporting medical devices, digital health, or other highly regulated electronic products in global markets. • Demonstrated knowledge of global telecommunications approval frameworks, including FDA-adjacent quality systems and product lifecycle compliance. • Familiarity with international regulatory authorities, certification bodies, and external test laboratory management • Experience serving as a technical mentor or subject matter expert in wireless technologies, regulatory strategy, or compliance program development.
For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.
Physical Job Requirements
The above statements are intended to describe the general
Tailor your resume for this Medtronic role before you apply.
Tailor my resume for this jobSimilar jobs
- Sr Regulatory Affairs Specialist — Dexcom · San Diego, California
- Sr Regulatory Affairs Specialist — Globus Medical · Audubon, PA
- RF Regulatory Engineer — Northwoodspace · Torrance, CA
- Sr Prin Regulatory Affairs Spec — Medtronic · Boston, Massachusetts, United States | London, London, United Kingdom
- Senior Regulatory Affairs Specialist — Siemens Healthineers · Remote
- Senior Regulatory Affairs Specialist — Iovancebiotherapeutics · Remote
- Senior Regulatory Affairs Specialist — Dexcom · San Diego, California
- Senior Regulatory Affairs Manager — Medtronic · Minneapolis, Minnesota, United States | Jacksonville, Florida, United States | Fort Worth, Texas, United States
More like this: More jobs at Medtronic · Browse all jobs
Free ATS checker · How to Tailor Your Resume to a Job Description (Step by Step)