Global Regulatory Affairs Specialist - Medical Devices
ICU Medical
ICU Medical is seeking a Regulatory Affairs professional to support global and US registrations of medical device products. You will analyze regulatory requirements, create and maintain registration dossiers, and ensure compliance across submissions and change management. You will coordinate with regional teams, prepare agency meeting packages, and lead regulatory strategy discussions while serving as a liaison to agencies and project teams. Travel up to 20% may occur. #J-18808-Ljbffr
- ICU Medical seeks a seasoned Regulatory Affairs professional to provide global and US registration expertise for electro-mechanical device products. You will analyze requirements, prepare registration dossiers, ensure documentation compliance, and support regulatory strategy...Medical device
- ICU Medical is seeking a regulatory professional to support global and US electronic publishing and submission of medical devices. You will help structure submissions, organize packages, and track deliverables under supervision, ensuring compliant documentation and change...Medical device
- ...Responsibilities: The Regulatory Affairs Level III (Senior Specialist) position is responsible for global product registrations and ensuring regulatory compliance... ...in the design, manufacturing, and sales of medical devices (including Class I and II devices,...Medical device
$61.3k - $122.7k
...Abbott is a global healthcare leader that helps people live more fully at all... ...businesses and products in diagnostics, medical devices, nutritionals and branded generic... ...and scientists. The Opportunity The Regulatory Affairs Specialist II (Medical Events) position supports...Medical deviceWorldwide- ICU Medical is seeking a Regulatory Affairs professional to support global and US registrations for medical devices. The role involves planning registration packages, liaising with agencies, and ensuring compliance across changes and submissions. Candidates should have...Medical device
- Abbott, a global healthcare leader, seeks a Regulatory Affairs Specialist II (Medical Events) in Lake Forest, IL on site. You will review and submit Medical Device Reports (MDRs) and vigilance reports, ensuring compliance with 21 CFR 803 and related regulations. You will...Medical device
$68k - $136k
Abbott is a global healthcare leader that helps people live more fully at all stages... ...and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...for millions of people. The Regulatory Affairs Specialist II is responsible for implementing and...Medical deviceWork experience placementWorldwide$68k - $136k
...AmericaTime Type: Full timeAbbott is a global healthcare leader that helps people... ...and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...Opportunity We are recruiting for a Regulatory Affairs Specialist III to join our team on-site in...Medical deviceWorldwideShift work$97.5k - $139.75k
...Position Summary Provides regulatory support and expertise associated with global and US registration of medical device products, including in-depth analysis of the requirements... ...agency review. Represents Global Regulatory Affairs at research and development meetings and...Medical deviceWork at officeLocal area$30 - $35 per hour
...Regulatory Affairs Associate/Specialist/Data Analyst I Client Industry: Pharmaceutical/Medical Device/Biotechnology; Job Title: Regulatory Affairs Associate/Specialist/Data Analyst I Location: North Chicago, IL 60064 (Hybrid; onsite Mon-Thu, remote Friday) Duration...Medical deviceHourly payContract workTemporary workRemote workRelocation- ICU Medical seeks a Regulatory Operations Specialist to provide regulatory support for global and US electronic publishing and submissions of medical devices. You will assist with creating and maintaining submission packages, tracking deliverables, and ensuring full regulatory...Medical device
- Abbott in Buffalo Grove, IL is seeking a Regulatory Affairs Specialist III to support day-to-day regulatory activities for new and existing medical devices. You will help develop global regulatory strategies, prepare US submissions, and ensure compliance with GMP and quality...Medical device
$113.3k - $226.7k
...HealthcarePosted Date: 2026-07-29Abbott is a global healthcare leader that helps people... ...and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...functional programs across Operations, Quality, Regulatory, Commercial, R&D, and Supply Chain....Medical deviceLive inRelocation package- Abbott in Lake Forest, IL is seeking a Regulatory Affairs Specialist II to implement and maintain the quality system and support change control... ...years of regulatory experience, with preferred background in medical devices or in-vitro diagnostics. #J-18808-Ljbffr AbbottMedical device
$149.3k - $298.7k
...DevelopmentIndustry: HealthcarePosted Date: 2026-08-26Abbott is a global healthcare leader that helps people live more fully at all... ..., with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues...Medical deviceWorldwide$99.3k - $198.7k
...AmericaTime Type: Full timeAbbott is a global healthcare leader that helps people live... ...and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...executive presentationsComplianceComplies with regulatory requirements, company policies, and...Medical deviceFor contractorsWork at officeWorldwideShift work$67.5k - $96.75k
Position Summary Provides regulatory support and expertise associated with global and US electronic publishing and submission of medical devices, including understanding the structure of the... ...with regional country Regulatory Affairs counterparts to evaluate and prepare...Medical device$80.9k - $127.05k
...What Regulatory Affairs contributes to Cardinal Health Regulatory provides... ...to enable pharmaceutical, medical and biotechnology... ...Principal Regulatory Affairs Specialist will support the Medical Solutions... ...aligned with global medical device regulations and the goals...Medical deviceFull timeTemporary workWork experience placementImmediate startRemote workFlexible hours$66 - $72 per hour
Job Title: Regulatory Affairs Associate I Job Description The Regulatory Affairs Associate I plays... ...in regulatory, pharmaceutical, or medical device environments. Experience in Regulatory... ...2, 2026. About Actalent Actalent is a global leader in engineering and sciences services...Medical deviceContract workTemporary workWork at officeRemote work$149.3k - $298.7k
...AmericaTime Type: Full timeAbbott is a global healthcare leader that helps people live... ...and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...with global R&D, software engineering, regulatory, quality, operations, and commercial organizations...Medical deviceWorldwideShift work$149.3k - $298.7k
...AmericaTime Type: Full timeAbbott is a global healthcare leader that helps people live... ...and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...software engineering, operations, quality, regulatory, and commercial organizations to deliver...Medical deviceWorldwideShift work$99.3k - $198.7k
About Abbott: Abbott is a global healthcare leader that helps people live more fully... ...changing technologies spans diagnostics, medical devices, nutritionals, and branded generic... ...presentations Compliance Complies with regulatory requirements, company policies, and operating...Medical deviceFor contractorsWork at officeWorldwide$29 - $32.29 per hour
job summary: Join the team as a Regulatory Affairs Associate with a top-tier global pharma leader in North Chicago,... ...., Pharmacy, Biology, Chemistry, Medical Technology, Pharmacology). ~0-2... ...experience in the pharmaceutical, medical device, or healthcare-related field. ~...Medical deviceHourly payContract workTemporary workWork experience placement$165k - $230k
Associate Director, Global Quality and Compliance Excellence BioSpace... ...issues today and address the medical challenges of tomorrow. We... ...to lead preparedness for regulatory inspections and audits at AbbVie... ...combination products, medical devices, tissue, and cosmetics for...Medical deviceFull timeTemporary workLocal area- ...Abbott Laboratories in Buffalo Grove, IL is seeking a Regulatory Affairs Specialist III to support regulatory direction for diabetes care products... ...have a bachelor’s degree in a technical field with 5+ years in medical devices and regulatory experience, #J-18808-Ljbffr...Medical device
- ...integration, risk assessment, and system validation for innovative drug/device combos. You will lead global engineering activities, collaborate with external partners, and ensure designs meet IEC/ISO and regulatory requirements while delivering robust patient-centric solutions....Medical device
- A global staff augmentation firm is seeking an experienced professional to join their Consumables R&D team in Lake Forest, Illinois... ...Engineering and 2-5 years of relevant experience, particularly in Medical Device Development. Key responsibilities include defining testing...Medical device
- ...Technology, Inc is seeking a detail-oriented Regulatory Affairs Consultant to join their team. This... ...regulatory strategies for U.S. and global markets, preparing essential... ...ensuring compliance with international medical device regulations. The ideal candidate will...Medical deviceContract workRemote work
$129.3k - $258.7k
Abbott is a global healthcare leader that helps people live more... ...products in diagnostics, medical devices, nutritionals and branded generic... ...the Medical & Scientific Affairs organization. We’re empowering... ..., Clinical Development, Regulatory, Marketing, and Commercial teams...Medical deviceWorldwideShift work$149.3k - $298.7k
Abbott is a global healthcare leader that helps people live more fully at all stages... ...and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...Partner with Commercial, Medical Affairs, R&D, Regulatory, Government Affairs and Marketing leaders...Medical deviceShift work
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