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
Vacancy posted 1 day ago
Similar jobs that could be interesting for youBased on the Global Regulatory Affairs Specialist - Medical Devices in Lake Forest, IL vacancy
- ...Pharmaceutical Recruiter. The ideal candidate will provide regulatory support for both U.S. and global medical device submissions, focusing on compliance with FDA and... ...and at least 2 years of experience in Regulatory Affairs within the medical device field are essential. #J-...Medical device
- 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 in Lake Forest, IL seeks a Global Marketing IVDR Project Coordinator to support administration of the IVDR program. You will... ...management experience, strong Excel skills, and 4-5 years in corporate settings; medical device exposure is a plus. #J-18808-Ljbffr AbbottMedical device
- Jobtailor is seeking a senior Regulatory Operations leader to manage the regulatory operations team and oversee data management for submissions... ...collaboration with cross-functional groups. You will develop global regulatory strategies, guide preparation and submission...Medical device
- What Regulatory Affairs contributes to Cardinal HealthRegulatory... ...pharmaceutical, medical and biotechnology companies... ...Regulatory Affairs Specialist will support the... ..., and maintenance of global product registrations... ...regulations for medical devices and advise on impact...Medical deviceFull timeTemporary workWork experience placementWork at officeLocal areaImmediate start
$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$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 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
- Senior Pharmaceutical Recruiter - Unicon Pharma Inc Regulatory Affairs Specialist Provide regulatory support for U.S. and global medical device submissions, including FDA and EU requirements. Prepare and organize registration packages and maintain global regulatory dossiers...Medical deviceContract 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$129.3k - $258.7k
...Type: Full timeAbbott is a global healthcare leader that helps... ...and products in diagnostics, medical devices, nutritionals and branded generic... ...the Medical & Scientific Affairs organization.We’re... ...Affairs, Clinical Development, Regulatory, Marketing, and Commercial teams...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... ...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- Title: Project Coordinator (Global Marketing - IVDR) Location: Lake Forest, IL Duration: 3+ Months 100% Onsite Job Summary: The Global... ...’ corporate environment experience 1-2 years’ experience in Medical device sector advantageous. Job Responsibilities: Responsible to...Medical deviceTemporary workFlexible hours
$113.3k - $226.7k
What You’ll Work On Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of... ..., with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues...Medical deviceWorldwide$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$78k - $156k
...HealthcarePosted Date: 2026-08-06Abbott is a global healthcare leader that helps people... ...and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...information on the IT Compliance needs and regulatory environment.What You’ll Work OnLeads the...Medical deviceWorldwide- ...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
- Nemera is a global leader in drug delivery systems and seeks a Program Manager in the Chicago area (Buffalo Grove, IL) to lead the Program Management team, coordinate project activity, and ensure NPI process compliance for mass production programs. You will drive project...Medical deviceWork at office
- ...and a minimum of 8 years of quality experience in pharma or medical device manufacturing. Key responsibilities include writing and maintaining... ...North Chicago, providing critical support to ensure compliance with corporate and regulatory standards. #J-18808-Ljbffr SPECTRAFORCEMedical 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
- ...Mundelein, IL is seeking an Adverse Event Specialist responsible for product complaint... ...eMDR, while coordinating with Quality, Regulatory Affairs, and R&D to gather needed information.... ...experience and offers a path within a global #J-18808-Ljbffr Medline Industries, LPMedical device
- ...seeking a detail-oriented, experienced Regulatory Affairs Consultant to join our team on a... ...help support both ongoing operations and global market expansion efforts. Role & Responsibilities... ..., ISO 13485, and international medical device requirements Reviewing labeling, IFUs...Medical deviceContract workRemote work
$40 per hour
job summary: Are you ready to take the next step in your regulatory career with a global healthcare technology leader dedicated to advancing patient care through cutting-edge medical devices? In this role, you will play a key part in coordinating global submissions and...Medical deviceHourly payContract workTemporary workWork experience placementRemote work- ...role, you will work closely with R&D, Regulatory, Operations, and other cross-functional... ...quality engineering experience in the medical device industry, including direct support of instrumentation... ...to work effectively across global, cross-functional teams, communicate clearly...Medical device
- ...026-07-27Medline in Mundelein, IL is seeking an Adverse Event Specialist to manage product complaint remediation and MDR reporting responsibilities... ....You will review historical and new complaints, determine regulatory obligations, and submit MDRs via the FDA eMDR portal while...Medical device
- ...product and process changes for quality and regulatory impact, and support change control... ...quality engineering experience in the medical device industry, including direct support of instrumentation... ...• Ability to work effectively across global, cross-functional teams, communicate...Medical device
- ...Remote50% RemoteRoles& Responsibilities:The Combination and Medical Device Products Consumable Device US team is expanding its support... ...-market supplier changes.Knowledge of applicable global regulatory requirements and industry standards (MDR requirements, ISO...Medical deviceWork at office
$220k - $250k
...results of your hard work? Lundbeck is a global biopharmaceutical company focusing... ...SUMMARY: The Director, US Regulatory Affairs Global Strategic Labelling will lead and... ...of experience within a pharmaceutical, medical device and/or biotech industry, with 7+ years...Medical deviceTemporary workWork at officeRemote workFlexible hoursLundbeck
Deerfield, ILa month ago
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Global Regulatory Affairs Specialist - Medical Devices. Be the first to apply!
Related searches
- regulatory contract Lake Forest, IL
- regulatory Lake Forest, IL
- regulatory law Lake Forest, IL
- medical device Lake Forest, IL
- code compliance Lake Forest, IL
- regulatory affairs part time Lake Forest, IL
- medical compliance Lake Forest, IL
- regulatory compliance Lake Forest, IL
- corporate compliance Lake Forest, IL
- compliance technician Lake Forest, IL