Global Regulatory Submissions Specialist
ICU Medical
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 management. Key duties include coordinating regulatory submissions with global leaders, preparing eSTAR registration packages, and aligning regional submissions with requirements while maintaining timelines and quality #J-18808-Ljbffr ICU Medical
- 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...Suggested
- ICU Medical is seeking a Regulatory Affairs professional to support global and US registrations of medical device products. You will analyze regulatory requirements... ...registration dossiers, and ensure compliance across submissions and change management. You will coordinate with...Suggested
$78.5k - $141k
Senior Associate Regulatory Affairs Submission Management - Hybrid Full-time Salary Min: 78500 Salary Max: 141000 Workday Global Grade: 16 Compensation: USD 78500 - USD 141000 - yearly About AbbVie AbbVie's mission is to discover and deliver innovative medicines...SuggestedFull timeTemporary workWork at officeLocal areaRemote work- Planet Pharma is seeking a Regulatory Information Management support professional in Illinois. The role focuses on regional regulatory submissions, system-based data stewardship, and ensuring alignment with central data standards. Fresh graduates with relevant life sciences...Suggested
- ...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...Suggested
- ...remarkable impact on people's lives. As a Global Trade Compliance organization, we are... ...classification requests for government submissions, ensuring accuracy and thoroughness.... ...tracking, interpreting, and communicating regulatory and legislative updates to GTC stakeholders...Full timeTemporary workLocal areaWorldwide
$61.3k - $122.7k
Abbott is a global healthcare leader that helps people live more fully at all stages... ...and scientists. The Opportunity The Regulatory Affairs Specialist II (Medical Events) position supports... ...timely review, documentation, and submission of Medical Device Reports (MDRs), including...Worldwide$68k - $136k
Abbott is a global healthcare leader that helps people live more fully at all stages... ...for millions of people. The Regulatory Affairs Specialist II is responsible for implementing and... ...and teams. Prepares U.S. regulatory submissions and/or registration documents for international...Work experience placementWorldwide- ...Instagram, X and YouTube. Job Description The Senior Manager Regulatory Affairs, Global Reg Strategy US & Canada (Hybrid) is responsible for the... ...responsible for the preparation and review of regulatory submissions consistent within US and Canada regulatory requirements...Local area
$109.5k - $208.5k
Manager, Regulatory Affairs Submission Management - Hybrid Full-time Salary Min: 109500 Salary Max: 208500 Workday Global Grade: 18 Compensation: USD 109500 - USD 208500 - yearly About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions...Full time- ICU Medical is seeking a Regulatory Affairs professional to support global and US registrations for medical devices. The role involves planning registration... ..., and ensuring compliance across changes and submissions. Candidates should have strong regulatory expertise...
- 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...
- ...Remote50% Remote Responsibilities: Support regional Regulatory Information Management (RIM) activities using... ...changes Commitment and obligation tracking Partner with global and regional teams to ensure regulatory submissions and correspondence are accurately documented and...Remote work
- AbbVie in the United States is seeking an Associate Director Regulatory Affairs, CMC to lead regulatory strategies and submissions for drug products. You will collaborate with internal teams and external partners, negotiating with agencies to enable first-pass approvals...
- ...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...Contract work
- ...Job Title: Regulatory Affairs Associate. Location: Lake Forest, IL Duration: 12 Months Pay Rate: $33-$... ...Provides regulatory support and expertise associated with global and US electronic publishing and submission of medical devices, including understanding the...Hourly pay
- ...Facebook , Instagram , X and YouTube. Job Description The Global R&D Study Forecasting Manager is responsible for managing the... ...outputs and analysis for Plan, LBE, LRP and Portfolio submissions. The manager establishes standards across the team by coordinating...Full timeLocal area
- AbbVie in North Chicago, IL is seeking a Director Regulatory Affairs Global Regulatory Lead to drive global strategies for development and lifecycle... ...teams to ensure regulatory readiness and compliant submissions. The role requires 7+ years in regulatory affairs, strong...
- AbbVie seeks a Director to drive regulatory data standards and governance, ensuring data quality and interoperability... ...ISO IDMP expertise and collaboration across global teams to enable compliant data submissions. You will lead governance processes, contribute to Enterprise...
$68k - $136k
...AmericaTime Type: Full timeAbbott is a global healthcare leader that helps people... ...Opportunity We are recruiting for a Regulatory Affairs Specialist III to join our team on-site in... ...teams as well as prepare US regulatory submissions and/or registration documents. Additionally...WorldwideShift work$67.5k - $96.75k
JOB DESCRIPTION Provides regulatory support and expertise associated with global and US electronic publishing and submission of medical devices, including understanding the structure of the electronic submission, organization of the submission package and tracking of deliverables...- Abbott in Lake Forest, IL is seeking a Regulatory Affairs Specialist II to implement and maintain the quality system and support change control... ...manufacturing/operations. You will prepare U.S. regulatory submissions and coordinate with international affiliates to secure...
- ...Libertyville, IL, seeks an experienced Trade Compliance Specialist to maintain and advance the global trade compliance program. The role coordinates import/export documentation, tariff classification, and regulatory reporting, partnering with logistics, procurement,...
- ...on LinkedIn, Facebook , Instagram , X and YouTube. Job Description The primary objective of this position is to lead Global Commercial Actuals Reporting P&L processes and consolidations. With the new organization structure combining US Therapeutics HQ...Full timeWork experience placementLocal area
$113.3k - $226.7k
...SupportIndustry: HealthcarePosted Date: 2026-07-29Abbott is a global healthcare leader that helps people live more fully at all stages... ...-wide, cross-functional programs across Operations, Quality, Regulatory, Commercial, R&D, and Supply Chain.Drive Global Business Excellence...Live inRelocation package- AbbVie is seeking a senior finance leader to drive the Global LBE planning process for the Commercial Controllership Organization. You will deliver analyses, recommendations, and decision support to ensure accurate consolidations of LBEs. The role requires coordinating...
- AbbVie is seeking a senior finance leader to own the Global Latest Best Estimates (LBE) planning for the Commercial Controllership Organization. You will provide financial analysis, recommendations, and decision-support, driving accurate consolidations and executive-ready...
- AbbVie North Chicago, IL is seeking a Senior Associate Regulatory Affairs Submission Management for a hybrid role. The position involves managing medium to high impact regulatory submission projects, coordinating cross-functional teams, and guiding publishing timelines...
- AbbVie North Chicago, IL is seeking a Senior Associate, Regulatory Affairs Submission Management to lead medium-to-high impact submission projects and coordinate cross-functional teams. You will plan timelines, ensure high-quality dossiers, and assist with publishing tasks...
- ...Reporting to the Associate Director for Privacy Compliance, Global Privacy Office, the “Privacy Manager, U.S." is an individual contributor... ...impact of evolving U.S. federal and state privacy legislation, regulatory guidance, and enforcement trends on AbbVie's business...Full timeWork at officeLocal area
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