Global Regulatory Affairs Specialist - Medical Devices
Baxter Healthcare Corporation
Baxter Healthcare is seeking a Principal Specialist, Global Regulatory Affairs to lead regulatory activities for a portfolio of medical device products in the U.S., EU, and globally. You will craft regulatory strategies, assess changes, and support submissions that maintain market access and compliance throughout the product lifecycle. You will collaborate with Regulatory Affairs, R&D, Quality, Marketing, and Operations, guiding submissions and lifecycle changes while ensuring regulatory #J-18808-Ljbffr Baxter Healthcare Corporation
$104k - $143k
...a job—you will find purpose and pride. Your role at BaxterAs a Principal Specialist, Global Regulatory Affairs, you will manage regulatory activities for an assigned portfolio of medical device products across the U.S., EU, and other global markets. You will develop regulatory...Medical deviceFull timeTemporary workWork visaFlexible hours- Baxter International Inc. in Round Lake, IL is seeking a Principal Specialist, Global Regulatory Affairs. You will manage regulatory approvals, registrations, and change assessments for medical device products across the US, EU, and other markets, shaping submission strategies...Medical device
$104k - $143k
...job—you will find purpose and pride. Your role at Baxter As a Principal Specialist, Global Regulatory Affairs, you will manage regulatory activities for an assigned portfolio of medical device products across the U.S., EU, and other global markets. You will develop regulatory...Medical deviceTemporary workWork visaFlexible hours$104k - $143k
...Principal Specialist in Regulatory Affairs at Baxter managing medical device product compliance and market access across US, EU, and global markets. Develops regulatory strategies, assesses product changes, and supports submissions throughout the device lifecycle while...Medical device- ...train our internal team on regulatory requirements, data collection... ...Finance, Sales, Marketing, Medical Affairs, Accounts Payable, Procurement... ...working in the medical device, pharmaceutical, biotechnology... ...Experience working in a global medical device or pharmaceutical...Medical deviceTemporary work
$70k - $80k
...Job Description Regulatory Analyst | Advanced Nuclear Energy |... ...is building a genuinely new global industry, deploying nuclear... ...Engineering, Legal, Government Affairs and Business Development \n... ...aviation, rail, defense, pharma, medical devices, financial services or...Medical deviceWork at office$39 - $42.18 per hour
...summary: Advance your career as a Regulatory Affairs Associate II with a Top-Tier Global Pharma Leader in North Chicago,... ...to deliver life-changing medical products to patients while managing... ...for Class III implantable medical devices. Handle government interactions...Medical deviceHourly payContract workTemporary workWork experience placement$90k - $105k
...Description Senior Regulatory Analyst | Advanced... ...building a genuinely new global industry, deploying... ...Legal and Government Affairs \n Represent the company... ...external counsel and specialist advisers, and review... ..., defense, pharma, medical devices, financial services...Medical deviceWork at office$149.3k - $298.7k
...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... ...security trends, the threat landscape, regulatory requirements, and industry best...Medical deviceTemporary workFor contractors$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- ...system-level Verification & Validation (V&V) activities for medical device products. The role involves planning and executing V&V activities... ...activities comply with applicable quality standards, regulatory requirements, and internal procedures. Collaborate with cross...Medical deviceRemote work
- ...Title - Sr. Validation Engineer Location - Round Lake IL Job Type - Contract Key Qualifications- 1) Experience in medical devices (probably infusion pumps) 2) strong system level V&V experience. 3) Ability to perform execution on validation activities....Medical deviceContract work
- ...pumps, sets, and software. You will guide a team of design quality professionals, set strategy, and ensure compliance with global regulatory standards while driving continuous improvement and collaboration across functions. The role emphasizes hands-on execution and...Medical device
- ...Project Engineer (Combination Products/Medical Devices) Location: North Chicago, IL 60064 Contract... ...Lake County, IL. The role is part of a global team and requires regular collaboration... ...management documentation aligned with regulatory standards ~ Create and manage Design...Medical deviceContract workLocal areaRelocationShift work
- ...and the department is following regulatory compliance requirements.... ...uses in projected products or devices. Qualifications • Knowledge of cGMP and global regulatory guidelines such as EMA... ...the pharmaceutical industry or medical device experience • BS in Science...Medical device
$96k - $140k
...and identify potential areas for improvements in the evolving Medical Device industry. You will build your professional experience by partnering... ...group contributing to the success of the process from a global perspective. The expectation is that you will learn all the various...Medical deviceWork at officeWorldwideNight shift$200k
...Job Description Associate Sales Representative – | Seattle \n Global medical device industry leader is hiring an Associate Sales Representative to join its high-performing surgical sales team in Seattle. \n This is an outstanding opportunity to break into medical...Medical device- ...– Pharmaceutical, Life Sciences and/or Medical Device Meetings & Events Full-Time | Midwest US... ...investigator meetings, sales meetings, congresses, global medical education programs, POAs sales... ...stakeholders across Commercial, Medical Affairs, Clinical Operations, Marketing,...Medical deviceFull time
- ...current best practices for use of regulatory business systems within the... ...for Class III implantable medical devices. Relies on extensive... ...including 1-2 years in regulatory affairs, R&D, or Manufacturing (CTD... ...all levels and types of global personnel required Experience...Medical devicePermanent employmentFull timeContract workShift work
$100k
...Description Mechanical Engineer Medical Device | Product Development & Innovation Medela... ...in accordance with quality and regulatory requirements. Work within a structured... ...requirements. Experience working in a global product development environment....Medical deviceLocal areaRemote work$130k - $150k
...management experience in lab/diagnostics/IVD). \n \n Join a global leader in medical diagnostics. Our client is a worldwide manufacturer of... ...Manager to support the growth. \n \n Medical device/equipment client in lab industry seeking Product Marketing...Medical deviceWorldwide$80k - $110k
...compliance with FDA, cGMP, GLP, USP, and other regulatory requirements. The supervisor drives... ...pertinent to pharmaceutical and medical device manufacturing labs. Must possess excellent... ...accommodations to individuals with disabilities globally. If, because of a medical condition or...Medical deviceTemporary workWork visaFlexible hours$104k - $143k
...cybersecurity design and analysis of multiple medical devices. Demonstrate subject matter expert... ..., Compliance, Clinical, Human Factors, Regulatory, Marketing, Service).Ensure compliance... ...to individuals with disabilities globally. If, because of a medical condition or...Medical deviceFull timeTemporary workWork visaFlexible hours3 days per week$176k - $242k
...product, it will touch a portion of our global operation.The mission of Baxter is to... ...company goals, industry standards, and regulatory requirements. Set and lead priorities within... ...knowledge to the advancement of the medical device industry.What you'll bringBachelor's in...Medical deviceOdd jobFull timeTemporary workLocal areaWorldwideFlexible hours- ...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
$168k - $231k
...at the forefront of innovation in the medical device industry, dedicated to improving patient... ...on software development and validation.Regulatory Knowledge: Demonstrate strong knowledge... ...accommodations to individuals with disabilities globally. If, because of a medical condition or...Medical deviceFull timeTemporary workLocal areaRelocation packageFlexible hours$112k - $154k
..., reliability, usability and regulatory compliance, as well as risk.... ...interdisciplinary design and development of medical products in compliance with... ...EU MDR, ISO 13485 and other global regulatory standards to... ...standards affecting medical devices and have experience with...Medical deviceFull timeTemporary workLocal areaWork visaFlexible hours$85k - $100k
...help shape the future of specialist recruitment across medical imaging, diagnostics, AI-... ...opportunity to join an established global life sciences recruitment... ...MedTech and Medical Devices recruitment division... ...across commercial, technical, regulatory, R&D, and software...Medical deviceVisa sponsorshipRelocation package$152k - $209k
...product, customer, quality, regulatory, and business priorities into... ...drives timely decisions across global teams.You will partner with R... ..., Quality, Regulatory, Medical, Manufacturing, Supply Chain,... ...in a highly regulated medical device environment.What You'll Be DoingLead...Medical deviceFull timeTemporary workLocal areaWork visaFlexible hours- ...the pharmaceutical, biotechnology, and medical device industry. Trinity’s Life Sciences consulting... ...to client satisfaction and our global team of experienced professionals, Trinity... ...life science industry. \n Knowledge of regulatory compliance inclusive of cGMP, 21 CFR...Medical deviceLocal areaImmediate startRelocation
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