Regulatory Affairs Intern — Medical Devices
$26.5 - $59 per hourWayne State University
A leading educational institution is offering a Regulatory Intern position in Santa Clara, California, for the summer of 2026. The role involves learning about regulatory processes in medical device development while supporting the Regulatory team with documentation and research. Candidates must currently be pursuing a relevant bachelor's degree and demonstrate strong technical writing and organizational skills. This internship offers an hourly pay range of $26.50 to $59.00, depending on experience. #J-18808-Ljbffr Wayne State University
$26.5 - $59 per hour
Regulatory Intern Location: Santa Clara, California, United States of America Term June to August... ...per week) Purpose The Regulatory Affairs Intern will learn about regulatory processes... ...Learn and demonstrate fundamentals of medical device development, design, clinical use, and...InternshipMedical deviceHourly payFull timeWork at officeLocal area- ...IntelliPro in Sunnyvale, CA is seeking a Regulatory Affairs Specialist 4 for a 6+ month engagement. You will develop regulatory plans, review... ...Health Canada filings. The ideal candidate has 8+ years in medical device regulatory affairs, deep knowledge of US, Canada and EU MDR...Medical device
- ...Sr. Regulatory Affairs Specialist We are searching for an experienced regulatory professional... ...experience working in IVD, Medical Devices or Pharmaceutical, with a history of... ...regulatory assessments and plans for international product registrations and approvals....Medical device
- ...Regulatory Specialist Our client, a leading organization in the medical device industry, is seeking a Regulatory Specialist to join their team. As... ...you will be part of the Regulatory Affairs Operations team supporting international labeling and compliance initiatives...Medical deviceWeekly payTemporary workFlexible hours
- Abbott seeks a Principal Regulatory Affairs Specialist to provide regulatory leadership for endovascular medical devices in Santa Clara, CA or Temecula, CA. You will manage regulatory activities across U.S., EU, and other markets, supporting lifecycle management and global...Medical device
- Apple Inc. in Cupertino, CA is seeking an International Regulatory Affairs Lead to head a team responsible for the international expansion of Apple Health’s regulated medical device features. This strategic role focuses on leading regulatory programs, developing global...Medical device
- ...treated? Join us as a Senior Regulatory Affairs Specialist and be at the... ...of regulatory science for medical robotics. Your mission? To... ...modified Class II and III devices and preparing and submitting... ...provides input related to FDA and international product registrations and...Medical deviceFull time
- Apple Inc. in Cupertino, California is seeking a Principal Regulatory Affairs Associate for their health products team. This role... ...regulatory initiatives to obtain approvals for innovative medical devices, requiring 10+ years of medical device regulatory experience...Medical device
- Abbott Laboratories is seeking a Principal Regulatory Affairs Specialist for the Vascular division, working on-site in Santa Clara, CA... ...through commercialization. The role requires 6-8 years in medical devices, experience with Class II/III devices, and strong collaboration...Medical device
- System One in Sunnyvale, CA seeks a Sr. Regulatory Affairs Specialist for a contract engagement. The candidate will craft regulatory plans... ...and at least 8 years of regulatory affairs experience in medical devices, with expertise in US, Canada, and EU MDR #J-18808-Ljbffr...Medical deviceContract work
- Abbott is hiring a Regulatory Affairs Specialist for their Vascular Division in Santa Clara, CA. This role focuses on supporting EU and US regulatory activities for endovascular medical devices used in treating peripheral artery disease. Ideal candidates should possess...Medical device
- BBG Ventures, LLC is seeking a Senior Regulatory Affairs Specialist to join their team in Sunnyvale, CA on a hybrid basis (3 days on-site... ...minimum of 8 years of regulatory affairs experience in the medical device sector and a strong understanding of U.S. regulations. This...Medical deviceFor contractorsRemote work
- ...Sr. Regulatory Affairs Specialist Established medical device company is looking to hire a Sr. Regulatory Affairs Specialist to join their growing team! Must... ...processes, and facilities. Collaborate with international counterparts to support global regulatory submissions...Medical device
- ...provides expert support for regulatory project management,... ...guidance in interpretation of international regulations. • Review, approve... ...Mentor and coach regulatory affairs specialists. • Track and report... ...Quality AssuranceExperience level: AssociateIndustry: Medical DeviceMedical deviceLocal areaWorldwideFlexible hours
- ...Regulatory Affairs Specialist 4 Primary Function of Position The Sr. Regulatory Affairs... ...FDA 510(k) premarket notifications, internal Letters to File, pre-submissions, Health... ...affairs experience working in a medical device company (can be in combination with a...Medical device
- System One is seeking a Regulatory Affairs Specialist IV in Sunnyvale, California to lead regulatory strategy and submissions for medical devices across the U.S., Canada, and global markets. You will support product development, design changes, lifecycle management, and...Medical device
$160k - $185k
...physicians, pre-clinical engineering, and regulatory affairs to understand user interactions,... ...related experience developing flexible medical device instruments; or equivalent... ...education/training, key skills, and internal equity, as well as location, market and...Medical deviceFull timeWork experience placementLocal areaFlexible hours- ...of Trade Compliance to lead its global program for medical devices and compliant supply chains. This executive will define strategy, govern policy, and partner with Regulatory Affairs to ensure FDA and international requirements are met while maintaining continuous patient...Medical device
- ...global leader in robotic-assisted surgery, seeks a Senior Regulatory Affairs Specialist to lead regulatory plans, assess design-change impacts... ...prepare regulatory submissions for the U.S., Canada, and international markets. You will collaborate with engineering and...Medical device
- ...Opportunity That Awaits You: The Principal Regulatory Affairs Specialist provides regulatory... ...practices to ensure compliance with FDA and international regulations, guidelines, and... ...ideal candidate would have had previous medical device experience and looking for potential...Medical deviceFull timeWork at office
- ...trade compliance framework for medical devices, instruments, accessories,... ...patient care, regulatory approvals, and global commercial... ...Partner with Regulatory Affairs and Quality to ensure trade... ...supply chains. ~ BS in Law, International Trade, Business, Supply Chain...Medical device
$40 per hour
...Regulatory Affairs Specialist Take your regulatory affairs experience to the next level with an exciting opportunity supporting innovative... ...systems • Laboratory research experience in an IVD medical device regulated environment strongly preferred • Understanding of...Medical deviceContract workTemporary workWork at officeWorldwideDay shift- ...meaningful technical challenges? As a Software Engineering Intern at Danaher, you’ll work alongside experienced engineers developing... ...feedback Producing documentation to support medical device regulatory processes Who This Is For Students graduating in 2026...InternshipMedical deviceRemote job
- ...solutions. The client seeks a Principal Regulatory Affairs Specialist to lead complex regulatory... ...submissions for Class III implantable devices and software-driven technologies. Responsibilities... ...). Ensure compliance for Class III medical devices, including software-embedded...Medical device
$90k - $180k
...SCJob Type: Full timeCategory: Regulatory AffairsIndustry:... ...and products in diagnostics, medical devices, nutritionals and branded generic... ...Career development with an international company where you can grow... ...function of a Senior Regulatory Affairs Specialist is to provide...Medical deviceWork experience placementWorldwide$114k - $228k
...businesses and products in diagnostics, medical devices, nutritionals and branded generic... ...to:Career development with an international company where you can grow the career... ...devices and peripheral stents.This Regulatory Affairs Manager position is an onsite opportunity...Medical deviceShift work$100k - $200k
...ClaraJob Type: Full timeCategory: Regulatory AffairsIndustry:... ...and products in diagnostics, medical devices, nutritionals and branded generic... ...Career development with an international company where you can grow... ...Principal Regulatory Affairs Specialist to join our Vascular...Medical deviceFor contractors$220.5k - $259.41k
...and build relationships with internal and external partners to... ...85 or FDA QSR, knowledge of regulatory approval process and requirements... ...of relevant experience in medical devices industry with at least 5 years... ..., Operations, Clinical Affairs, Marketing, Quality, etc.)Excellent...Medical deviceFull timeContract workWork at office$81.5k - $141.3k
...businesses and products in diagnostics, medical devices, nutritionals and branded generic... ...to:Career development with an international company where you can grow the career... ...is seeking a passionate, experienced Regulatory Affairs Specialist to join our Vascular Division...Medical deviceFor contractorsShift work$31 per hour
...Function: Job Sub Function: Non-LDP Intern/Co-Op Job Category: All Job Posting Locations... ...May collaborate with R&D, marketing, regulatory, and clinical teams to align product... ...Demonstrated interest in healthcare, medical devices, or life sciences industries. Strong analytical...InternshipMedical deviceHourly payFull timeH1bWork at officeLocal area
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