Global Regulatory Affairs Senior Associate Medical Devices
ICU Medical
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 with cross-functional teams. You will liaise with regulatory agencies, evaluate manufacturing changes for regulatory impact, and represent Global Regulatory Affairs at R&D meetings. #J-18808-Ljbffr
- ...Abbott in Lake Forest, IL seeks a Principal Regulatory Affairs Specialist (Medical Events) to oversee timely review, documentation, and filing of Medical Device Reports including international vigilance for the division's products. You will ensure compliance with MDR...SeniorMedical device
$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...SeniorMedical deviceContract workWork at officeWorldwideRelocation package- ...Job Description Position: Senior Pricing & Compliance Specialist (Global Law Firm) \n Location: New York, NY (Hybrid WFH) \n Company: Globally Recognized Am Law Firm \n Comp Package: Base salary up to $130K, Bonus, Full Benefits, 401K+, etc. \n \n Summary...SeniorWork from home
$154k - $231k
...Senior Manager Regulatory Compliance# Medline Careers## Senior Manager Regulatory ComplianceApply... ...Laboratory Quality Assurance Unit to assure global regulatory compliance with... ...controlling risks on a global level for medical devices, cosmetics, and OTC drugs.**Job...SeniorMedical deviceMinimum wageFull timeWork experience placementLocal areaWorldwide- ...activities for New Product Introductions (NPI) of combination products and medical devices, ensuring on-time delivery and compliance with global regulations. You will collaborate with Regulatory, Product Development, and manufacturing teams to establish design controls...SeniorMedical device
- Job Title: Regulatory Affairs Associate Duration: 5 months Location: North Chicago, IL - Hybrid - (Tues... ...with all levels and types of global personnel required Experience working... ...manufacturing changes for Class III implantable medical devices. May require an advanced degree and...Medical deviceShift work
$129.3k - $258.7k
...2026-10-05 Abbott is a global healthcare leader that helps... ...in diagnostics, medical devices, nutritionals and branded... ...executives, and scientists. SENIOR MANAGER, Diagnostics PUBLIC AFFAIRS, Abbott (PUBLIC... ...stakeholders including regulatory affairs, operations, quality...SeniorMedical device$190k - $380k
...AmericaTime Type: Full timeAbbott is a global healthcare leader that helps people live... ...businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines... ....JOB DESCRIPTION:The OpportunityThe Senior Director, Commercial Operations and Enablement...SeniorMedical deviceShift work$78k - $156k
...Full timeAbbott is a global healthcare leader that... ...products in diagnostics, medical devices, nutritionals and... ...What You’ll Work OnThe Senior Statistician works with... ...Participate in data review and regulatory submission.Propose... ....JOB FAMILY:Clinical Affairs / StatisticsDIVISION:...SeniorMedical deviceWorldwideShift work- ...teams to ensure technical robustness and regulatory compliance throughout the product... ...MS with 8+ years, specifically within medical devices or combination products. Must possess expertise... ...and PCB design, embedded systems, and global regulatory standards like ISO 13485....SeniorMedical deviceTemporary work
- ...Summary The QA Senior Specialist will provide... ...corporate standards, regulatory requirements, and... ...Coordinate with centralized/global quality functions to... ...including activities associated with new market... ...pharmaceutical, biotechnology, medical device, or related regulated...SeniorMedical deviceFor contractors
- ...BioSpace is seeking a senior Electrical Systems Lead to drive the design of on-body... ...cross-functional teams, you will navigate regulatory requirements such as ISO 13485 and... ...risk assessments, design verifications, and validations for medical devices. #J-18808-Ljbffr...SeniorMedical device
$165k
...A global medical device manufacturer is seeking a Senior Automation Engineer to lead initiatives in multiple manufacturing sites. The role requires strong expertise in automation engineering, equipment design, and collaboration with various teams. Candidates should possess...SeniorMedical device$129.3k - $258.7k
...AmericaTime Type: Full timeAbbott is a global healthcare leader that helps people live... ...businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...more than 160 countries.JOB DESCRIPTION:Senior Manager, Commercial Sales...SeniorMedical deviceWorldwideShift work$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 OpportunityThe Senior Manager, Cybersecurity is responsible... ...national and international regulatory compliances and frameworks...SeniorMedical deviceWorldwideShift work$78k - $156k
...HealthcarePosted: 2026-10-27Abbott is a global healthcare leader that helps... ...products in diagnostics, medical devices, nutritionals and branded... ....The Opportunity The Senior Analyst, Pricing works out of... ...requirements of business policies and regulatory guidelinesWork with multiple...SeniorMedical devicePrice workContract workImmediate startWorldwide$86.7k - $173.3k
...Full timeAbbott is a global healthcare leader that... ...in diagnostics, medical devices, nutritionals and branded... ...other conditions. The Senior Quality Auditor is... ...ISO, FDA, and other regulatory agencies. Responsible... ...internal/external business associates reflects positively...SeniorMedical deviceWork experience placementLocal areaWorldwideShift work- ...Computational Modeling expert to advance SI/PI, EMC, and system-level modeling for medical device applications. You will drive simulation-driven design to reduce prototyping and accelerate regulatory submissions, collaborating across hardware, firmware, systems, and...SeniorMedical device
$78k - $156k
...Warehouse Plc / Controls EngineerAbbott is a global healthcare leader that helps people live more fully at all stages of life. Our... ..., with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues...SeniorMedical deviceWork experience placement$96.5k - $183.5k
...Transformation Senior Process Engineer- API Full... ...Max: 183500 Workday Global Grade: 17 Compensation... ...today and address the medical challenges of tomorrow... ...during Regulatory Agencies Audits. Responsible... ...health care, medical devices, pharmaceutical, biologics...SeniorMedical deviceFull timeTemporary work- Working with R&D, manufacturing, regulatory affairs and other functions, you will implement and maintain high quality standards and lead audits to ensure continued compliance and process improvements. #J-18808-LjbffrSeniorMedical device
- Overview Join to apply for the Senior Analyst, Compliance Analytics role at BioSpace... ...as required. Supports other global OEC initiatives and operational activities... ...priorities. Knowledge of pharmaceutical and medical device regulatory landscape (e.g., FDA, PhRMA, OIG, PDMA...SeniorMedical deviceTemporary work
- ...approval of manufacturing changes for Class III implantable medical devices. May require an advanced degree and 3 to 5 years of direct... ...: 6 years pharmaceutical experience including 5 years in regulatory affairs or 5 years in Discovery, R&D, or Manufacturing Experience...Medical deviceFor contractors
- ...the United States is seeking a Senior Scientist I, Engineering – Design... ...Team to advance new drug/device products. You will lead verification... ...collaborate across Quality, Regulatory, Clinical teams. This role requires 10+ years in medical devices, GMP knowledge, and...SeniorMedical device
- ...for an experienced Senior Scientist I Engineering... ...exciting new drug / device combination products... ...and procedures regulatory and safety requirements... ...Quality Regulatory Affairs Clinical Team and global partners Qualifications... ...of experience in medical device or...SeniorMedical deviceFull timeTemporary workLocal area
- ...DESCRIPTION The Senior Marketing... ...execution across ICU Medical's Infusion... ...Service, Clinical Affairs, and Executive... ..., healthcare associations, technology... ...Clinical Affairs, Regulatory Affairs, and... ...in medical device marketing, product... ...we are now a global market leader...SeniorMedical device
- ...and address the medical challenges of... .... AbbVie’s R&D global trial footprint... ...report to RDQA Associate Director or RDQA... ...The RDQA AREA Senior Manager will provide... ...state of regulatory preparedness. Ensure... .../ medical device industry experience... ..., regulatory affairs, clinical research...SeniorMedical deviceLocal area
$149.3k - $298.7k
...HealthcarePosted: 2026-10-23 Abbott is a global healthcare leader that helps people live... ...businesses and products in diagnostics, medical devices, nutritionals and branded generic... ...for Participating with other Abbott senior leaders to establish strategic plans and...Medical devicePermanent employmentWorldwide$113.3k - $226.7k
## Senior Product Manager - OncologyApply: United States - Illinois - Lake Forest: Full... ...time: Posted Today: 31163037Abbott is a global healthcare leader that helps people live... ...businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines...SeniorMedical deviceFull timeWork experience placementLocal areaWorldwide- ...under the Quality Dossier Program. You will interact with Medical Writing, Regulatory Affairs, and Development Sciences and manage audit schedules,... ...reporting. The role requires 5+ years in pharma/medical devices, QA auditing experience, and strong coordination across...SeniorMedical device
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