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
- ...Regulatory Affairs SpecialistResponsible for filing necessary applications and handling all government interactions pertaining to the... ...approval of manufacturing changes for Class III implantable medical devices. May require an advanced degree and 5-8 years of direct experience...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- 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
$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... ...lab results for millions of people. The Regulatory Affairs Specialist II is responsible for implementing...Medical deviceWork experience placementWorldwide$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$129.3k - $258.7k
...Date: 2026-07-06Abbott is a global healthcare leader that helps... ...and products in diagnostics, medical devices, nutritionals and branded... ...within the Medical & Scientific Affairs organization.We’re... ...Affairs, Clinical Development, Regulatory, Marketing, and Commercial teams...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$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
...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$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$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$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$113.3k - $226.7k
Abbott is a global healthcare leader that helps people live more fully at all stages... ...businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...programs across Operations, Quality, Regulatory, Commercial, R&D, and Supply Chain....Medical deviceLive inRelocation package$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$35 per hour
...Advance your career with a Top-Tier Global Pharma Leader in North Chicago, IL! This... ...2-year hybrid contract role as a Regulatory Affairs Associate II offers the opportunity to drive CMC... ...comprehensive benefits package, including: medical, prescription, dental, vision, AD&D,...Hourly payContract workTemporary workWork experience placement- ...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
- What Regulatory Affairs contributes to Cardinal HealthRegulatory provides... ...to enable pharmaceutical, medical and biotechnology... ...for regulatory activities associated with new product development... ...responsibilities aligned with global medical device regulations and the goals...Medical deviceFull timeTemporary workWork experience placementLocal areaImmediate startRemote work
- 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
$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- ...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
- ...Related Subject 2. 2-4 years CMC Regulatory experience - Bachelors Degree... ...Teams as needed The Senior Associate, RA CMC works with internal... ...relationships within the Regulatory Affairs functional areas and the... ...supervision. Responds to global regulatory information requests...Remote work
$78k - $156k
Abbott is a global healthcare leader that helps people live more fully at all stages... ...businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...on the IT Compliance needs and regulatory environment. What You?ll Work On Leads...Medical deviceWorldwide$160k - $180k
...Location: LibertyvilleDepartment: Operations SummaryLead the Global Indirect Procurement function through the development and... ...OE and cross-functional supply planning processes.Healthcare, medical device, or regulated manufacturing experience preferred.CompetenciesBe...Medical deviceContract workWork at officeWorldwideRelocation package- ...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
- ...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
- US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To... ...required for protocol and report writing. 3-5 years of experience in Medical Device Development. Must know Design Controls, Product Development...Medical device
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