Global Medical Devices Regulatory Affairs Associate
Unicon Pharma Inc
A leading pharmaceutical company located in Lake Forest, Illinois, is seeking a Senior Pharmaceutical Recruiter. The ideal candidate will provide regulatory support for both U.S. and global medical device submissions, focusing on compliance with FDA and EU requirements. Responsibilities include preparing registration packages, maintaining global regulatory dossiers, and collaborating across functions to resolve documentation issues. A Bachelor's degree and at least 2 years of experience in Regulatory Affairs within the medical device field are essential. #J-18808-Ljbffr Unicon Pharma Inc
- 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...Medical device
- ...Job Title: Regulatory Affairs Associate. Location: Lake Forest, IL Duration: 12 Months Pay Rate: $33... ...regulatory support and expertise associated with global and US electronic publishing and submission of medical devices, including understanding the structure of...Medical deviceHourly pay
- ...Pharmaceutical Recruiter - Unicon Pharma Inc Regulatory Affairs Specialist Provide regulatory support for U.S. and global medical device submissions, including FDA and EU... ...devices (RAC preferred). Seniority level: Associate Employment type: Contract Job function:...Medical deviceContract work
- 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
- ...Regulatory Affairs Specialist Responsible for filing necessary applications and handling all government interactions pertaining to... ...approval of manufacturing changes for Class III implantable medical devices. May require an advanced degree and 5-8 years of direct experience...Medical device
$68k - $136k
...AmericaTime Type: Full timeAbbott is a global healthcare leader that helps people... ...businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...results for millions of people. The Regulatory Affairs Specialist II is responsible for...Medical deviceWork experience placementWorldwideShift work- 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
$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, 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
$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$61.3k - $122.7k
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... ...and scientists. The Opportunity The Regulatory Affairs Specialist II (Medical Events) position...Medical deviceWorldwide$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$129.3k - $258.7k
...AmericaTime Type: Full timeAbbott is a global healthcare leader that helps people live... ...and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...opportunities.Work closely with R&D, clinical, regulatory, and commercial teams to ensure...Medical deviceLocal areaWorldwideShift work$149.3k - $298.7k
...HealthcarePosted Date: 2026-08-03Abbott is a global healthcare leader that helps people... ...and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...with global R&D, software engineering, regulatory, quality, operations, and commercial organizations...Medical deviceWorldwide$149.3k - $298.7k
...HealthcarePosted Date: 2026-08-03Abbott is a global healthcare leader that helps people... ...and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...software engineering, operations, quality, regulatory, and commercial organizations to deliver...Medical deviceWorldwide$165k - $230k
Associate Director, Global Quality and Compliance Excellence BioSpace - AbbVie -... ...issues today and address the medical challenges of tomorrow. We... ...regulations to lead preparedness for regulatory inspections and audits at... ...products, medical devices, tissue, and cosmetics for...Medical deviceFull timeTemporary workLocal area$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- ...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
- ...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
$78k - $156k
...AmericaTime Type: Full timeAbbott is a global healthcare leader that helps people live... ...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 deviceWorldwideShift work$68k - $136k
...AmericaTime Type: Full timeAbbott is a global healthcare leader that helps people... ...businesses 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-...Medical deviceWorldwideShift work- ...and prepare submissions via eMDR, while coordinating with Quality, Regulatory Affairs, and R&D to gather needed information. The role requires a Bachelor’s degree with 1+ year of relevant experience and offers a path within a global #J-18808-Ljbffr Medline Industries, LPMedical 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
- ...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
- ...Remote Responsibilities: Support regional Regulatory Information Management (RIM) activities... ...and obligation tracking Partner with global and regional teams to ensure regulatory... ...Requirements: Bachelor's degree in Regulatory Affairs, Pharmacy, Health Sciences, or a related...Remote work
- ...Assures proper integration and support of device regulations, drug regulations, and as... ...comprehensive understanding of combination products, medical devices, and design controls.Sound... ....Ability to work independently and in a global team environment, and with all levels of...Medical device
$99.3k - $198.7k
...Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies... ..., with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000...Medical deviceRemote work- ...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
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