Regulatory Affairs Specialist - Medical Devices (Global)
Medtronic
Medtronic is seeking an Associate Regulatory Affairs Specialist in Lafayette, CO, focusing on regulatory activities for their medical device product portfolios. This role involves working with R&D, Quality, and Marketing teams to ensure compliance and facilitate product submissions. The ideal candidate will hold a Bachelor’s degree and have at least 2 years of relevant experience in regulatory affairs. Experience with medical devices and regulations is preferred. Join us in making a difference in patient care. #J-18808-Ljbffr
- ...organization. Must Have Experience in medical device regulatory Proven ability to develop and... ...materials The Job The Principal Regulatory Affairs Specialist (Pr. RAS) is responsible for... ...Supports submissions and inquiries for global market. Collaborates closely with cross...Medical device
- ...Overview This Associate Regulatory Affairs Specialist (RAS) is based in Lafayette, CO within the Acute... ...Support submissions and inquiries for global markets. Collaborate with partners... ...experience. Nice to Have Experience in medical device regulatory affairs. Strong...Medical deviceLocal areaRemote work
- ...Medtronic is seeking a Principal Regulatory Affairs Specialist to provide regulatory leadership for core... ...in Lafayette, CO. You will lead global regulatory strategies and serve as a... ...degree and significant experience in medical device regulatory affairs. The position allows...Medical device
- ...Regulatory Affairs Specialist II Principal Duties and Responsibilities Assist with assembly, distribution... ...for compliance with applicable global regulations. Write and manage the development... ...abreast of regulations pertinent to medical devices, biologics, drugs and combination...Medical deviceWork at office
- ...Senior Regulatory Affairs Specialist Job Description This person will be joining a small, but mighty... ...labeling for compliance with applicable global regulations. Review proposed product... ...of experience in orthopedic or medical device industry. A minimum of 5 years of experience...Medical device
$160.8k - $241.2k
...Principal Global Upstream Product Manager At Medtronic you... ...emerging technologies, and regulatory trends to inform product strategy... ...Strategy Partner with Medical Affairs to shape clinical evidence... ...medical technologies or medical devices Experience influencing...Medical deviceWork at officeLocal areaFlexible hours- ...Highridge Medical LLC in Westminster, Colorado, seeks a Regulatory Affairs professional to assist with the regulatory submissions process and manage compliance with regulations for medical devices. The candidate should have a Bachelor's degree in life sciences, preferably...Medical device
- ...Highridge Medical LLC in Westminster, Colorado, is seeking a Regulatory Affairs Specialist II. This role involves developing regulatory strategies, assisting with submissions, and ensuring compliance with regulations. Candidates should have at least 3 years of experience...Medical device
$140k - $160k
...world-class engineers who have designed and tested firearms, medical devices, robots, cars, satellites, rockets, and supersonic jets; expert... ...you figure out how to get it all done. ABOUT THE ROLE As a Global Sourcing and Supply Chain Manager (GSSM) at Biofire, you’ll sit...Medical devicePermanent employmentFull timeWork at officeImmediate startWork from homeFlexible hours$160.8k - $241.2k
...future growth. The Principal Global Upstream Product... ...emerging technologies, and regulatory trends to inform product strategy... ...Strategy Partner with Medical Affairs to shape clinical evidence strategies... ...technologies or medical devices Experience influencing...Medical deviceH1bWork at officeLocal areaFlexible hours- ...This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe, support of international product registrations and related regulatory affairs activities, including execution of procedures and systems...Medical deviceWork at office
- ...Responsibilities: The Associate Regulatory Affairs Manager will support the... ...regulatory documents for medical device and IVD products. This... ...FDA, ISO 13485, and other global regulatory requirements.... ...to junior staff or specialists on assigned projects....Medical deviceWork at office
- ...Title: Website Content Marketing Specialist Client: Medical Device Manufacturing Industry Duration... ..., UX, SEO, tech, clinical, regulatory) to deliver cohesive and high-performing... ...requirements Support global content strategy including localization...Medical deviceFull timeShift workDay shift
$74.4k - $111.6k
## Regulatory Affairs Specialist - On-siteApplyremote type: Onsitelocations: Lafayette, Colorado, United States of Americatime type: Full timeposted... ..., compassionate world.# **A Day in the Life** Across our global Neuroscience organization, we advance care for some of...H1bWork at officeLocal areaWorldwideFlexible hours$74.4k - $111.6k
...connected, compassionate world. A Day in the Life Across our global Neuroscience organization, we advance care for some of... ...workflows, and support improved patient outcomes worldwide. The Regulatory Affairs Specialist is an individual contributor role within the Cranial &...H1bWork at officeLocal areaWorldwideFlexible hours$35 - $45 per hour
...Solutions Services, LLC is seeking a Test Engineer I for a 10-month contract in Lafayette, CO. The role involves ensuring cutting-edge medical products meet quality and reliability standards through verification and validation activities. Candidates must have a BS/BA in...Medical deviceHourly payContract work$19.5 - $21 per hour
...As a global medtech company, we are driven by our Vision of changing the trajectory of lives... ...LivaNova! LivaNova is a global medical technology company built on nearly five... ...and advanced cardiovascular medical devices. We hire individuals who are looking for...Medical deviceWorldwideShift work- ...Planet Pharma Group is seeking a Cybersecurity Specialist in Lafayette, Colorado. This role focuses on ensuring secure product design, working with medical device teams to create security documentation, and maintaining security throughout product lifecycles. Candidates...Medical deviceWork at office
- ...The Principal Regulatory Affairs Specialist (Pr. RAS) is responsible for collaborating, planning and... ...directly with FDA Strong experience with medical devices that have integrated software with... ...submissions and inquiries for global market. Collaborates closely with cross...Medical deviceRemote work
- ...A dynamic medical device organization located in Westminster, Colorado, is looking for an entry-level Regulatory Associate to join their team in July 2026. This in-office position involves assisting with US and international regulatory submissions, reviewing documentation...Medical deviceWork at office
- ...Embedded Software Engineer for its Lafayette, CO location. The candidate will design and develop software for next-generation medical devices, ensuring high performance and reliability. This role involves collaboration with cross-functional teams and requires strong expertise...Medical deviceFull time
- ...Regulatory Associate page is loaded## Regulatory Associatelocations: US CO Westminstertime... ...operational facets of a regulatory affairs career. As an RA team member, you will... ...writing skills, and immerse yourself in a medical device organization committed to its customers...Medical deviceWork at officeLocal area
- ...Job Title: Sr Controls Engineer – Medical Device Location: Lafayette, CO (Onsite) Type: W2 Contract Duration: 2-Year We are looking for a Manufacturing/Controls Engineer with experience in Industrial Automation, Ignition Platform, and Manufacturing Data Integration...Medical deviceContract work
$116k - $174k
...world. A Day in the Life Our space, the medical device and healthcare industry, is rapidly... ...arise. The Principal BP Project Management Specialist will play a crucial role in executing... ...Experience working with cross functional global teams Experience in Supply Chain,...Medical deviceH1bWork at officeLocal areaRemote workFlexible hours- ...integrate medium voltage and safety-critical systems for medical devices 2. Medical Device Regulatory Compliance & Safety Standards (IEC 60601) Hands-on... ...firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the...Medical deviceContract workWorldwide
$110k - $145k
...ideas to life—from advancing space exploration and life-saving medical devices to building autonomous electric vehicles. With 3,000+ experts... ...commercial vehicles, EVs, rail, and more. As part of the global ALTEN Group—57,000+ engineers in 30 countries—we deliver...Medical deviceFor contractors- ...Itlearn360 in Longmont, CO is looking for Cleanroom Technicians to assemble life-saving medical devices in a clean, high-tech environment. The role requires attention to detail, regulatory compliance, and experience in medical device assembly. Candidates should be...Medical device
- ...Job Description Job Description Job Title: Test Technician Client: Medical Device Manufacturing Industry Location: Lafayette, CO 80026 Duration: 12 Months (Possible Extension) Shift: 1st Shift Key Responsibilities • Set up test equipment, fixtures...Medical deviceContract workShift workDay shift
- ...A medical device company is seeking a Principal Regulatory Affairs Specialist to oversee regulatory activities for the INVOS™ Cerebral/Somatic Oximetry product line. The role requires at least 7 years of regulatory experience within medical devices. The successful candidate...Medical device
$19.5 - $21 per hour
Assembly Technician I Job Summary: The Assembly Technician I will work under general supervision to assemble and package product components, handle materials, and operate manufacturing equipment while following established policies, practices, and procedures. Responsibilities...Medical deviceHourly payShift work
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