Global Medical Device Regulatory Strategist - Contract
Next Generation Technology, Inc
Next Generation Technology, Inc is seeking a detail-oriented Regulatory Affairs Consultant to join their team. This position involves developing regulatory strategies for U.S. and global markets, preparing essential documentation for FDA submissions, and ensuring compliance with international medical device regulations. The ideal candidate will have a Bachelor’s degree and over 5 years of experience in regulatory affairs within the medical device industry. Both on-site and remote work options are available. #J-18808-Ljbffr Next Generation Technology, Inc
- Position Global Marketing Lead Manager Location Vernon Hills, IL... ...0.00 Shift 1st Shift Client Medical Device Company Job Category... ...Senior Level Employment Type Contract on W2 (Need US Citizens or GC... ...submissions background and Regulatory background dealing with claims...Contract workRegulatoryMedical deviceShift workDay shift
- ...a detail-oriented, experienced Regulatory Affairs Consultant to join our team on a contract basis. The opportunity is preferred... ...both ongoing operations and global market expansion efforts. Role... ..., ISO 13485, and international medical device requirements Reviewing...Contract workRegulatoryMedical deviceRemote work
$220k - $250k
...results of your hard work? Lundbeck is a global biopharmaceutical company focusing... ...SUMMARY: The Director, US Regulatory Affairs Global Strategic Labelling will... ...of experience within a pharmaceutical, medical device and/or biotech industry, with 7+ years...RegulatoryMedical deviceTemporary workWork at officeRemote workFlexible hours- ...Pharmaceutical Recruiter – Unicon Pharma Inc Regulatory Affairs Specialist Provide regulatory support for U.S. and global medical device submissions, including FDA and EU... ...Seniority level: Associate Employment type: Contract Job function: Analyst Industries: Medical...Contract workRegulatoryMedical device
- ...doing: The Associate General Counsel—Global Procurement & Real Estate will provide... ...Duties and Responsibilities Commercial Contracting Draft, review, negotiate, and... ...experience supporting a pharmaceutical and/or medical device company will be desirable. ~...Contract workMedical deviceTemporary workFlexible hours
- ...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...RegulatoryMedical device
- ...lead supplier quality activities across a global network of contract manufacturers, suppliers, and service providers supporting medical device, combination product, and... ...Agreements to ensure alignment with quality, regulatory, and business requirements Partner with...Contract workRegulatoryMedical deviceWork at officeRemote work3 days per week
$95k - $125k
...and health. From hearing devices, hearing implants and... ...supporting alignment with global category strategies. This... ...‑time Benefits Include Medical, dental, prescription, and... ...follow‑up. Ensure contract compliance and alignment with regulatory requirements (ISO 13485/...Contract workRegulatoryMedical deviceFull timeTemporary workWork at officeMonday to FridayFlexible hours$19 per hour
...Through a network of over 50 facilities globally, STERIS AST has been committed to providing contract sterilization services to the medical device, pharmaceutical, consumer, and... ...Skills Subject to passing Nuclear Regulatory Commission (NRC) required background check...Contract workRegulatoryMedical deviceTemporary workFor contractorsLocal areaRotating shift$130k - $155k
...your hard work? Lundbeck is a global biopharmaceutical company... ...delivery, issue escalation, contract management and continuous improvement... ...operational standards, and regulatory requirements. Build... ...within the pharmaceutical, medical device or healthcare industries....Contract workRegulatoryMedical deviceFlexible hours$30 - $33 per hour
...Job Description Auditor Contract: Long Grove, Illinois, US Salary Range... ...collaborate with complaint handling, regulatory, and quality teams to ensure corrective... ...Quality Auditing experience within the medical device, pharmaceutical, or healthcare industry...Contract workRegulatoryMedical deviceHourly payTemporary workWork at office- ...MMS Infusion business of a client in the medical devices industry. Key Responsibilities Support the regional MMS sales contracts lifecycle, including provision of lead information... ...recognition guidance, internal audit, regulatory controls, and business strategy....Contract workRegulatoryMedical deviceRemote jobWork at officeShift workDay shift
- ...Location - Vernon Hills, IL Duration – 10+ Months Contract Client: Medical Device Company Employment Type: Contract on W2 (Need US Citizens... ...are not limited to: Assist in the support of Quality, Regulatory & R&D to ensure systems are compliant with all internal...Contract workRegulatoryMedical deviceWork at office
$85k - $128k
...SEC guidance. Collaborate closely with Global Internal Controls and IT Governance, Medline... ...as well as emerging industry and regulatory risks. Exhibit the highest standards of... ...within a healthcare, life sciences, or medical device manufacturing/distribution environment....RegulatoryMedical deviceMinimum wageLocal area$129k - $259k
Senior Manager, Global Commercial Training $129K - $259K Abbott is a global healthcare... ...and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...development process that meets FDA and other regulatory requirements. Provide leadership and...RegulatoryMedical deviceWorldwideShift work$110k - $120k
...Recruiter/Sales Executive Manufacturing | Medical Devices We are seeking an experienced... ...to support a regulated medical device contract manufacturing environment. This role will... ...a strong focus on plant‑floor safety, regulatory compliance, and safety culture. This position...Contract workRegulatoryMedical deviceFull timeLocal area- ...Location: Vernon Hills, IL Duration: 10+ Months Contract Total Hours/week: 40.00 1st Shift Client: Medical Device Company Job Category: Quality Level Of... ...systems Working Knowledge of Quality Systems Regulatory requirements and application to Company /Unit requirements...Contract workRegulatoryMedical deviceH1bWork at officeDay shift
- ...Packaging Engineer Location Vernon Hills, IL Contract 12+ Months Contract Hours 40 hours per... ...Packaging design development for medical devices or pharma industry Packaging... ...medical devices Packaging standards and regulatory requirements for medical devices (i.e....Contract workRegulatoryMedical deviceTemporary workFor contractorsWork at officeRemote workFlexible hoursDay shift
- Ul Solutions is seeking a Senior Global Corporate Travel Specialist to lead our multi-national corporate travel program, ensuring comprehensive travel strategies aligning with global security and finance. This full-time hybrid role requires three days in-office at our...Full timeWork at office
- ...integration. Ensure systems comply with safety, quality, and regulatory requirements. Manage, mentor, and develop automation... ...assembly/processing/manufacturing companies or contract manufacturing, e.g. medical devices, pharmaceutical, automotive, or food processing....Contract workRegulatoryMedical deviceFlexible hours
- A reputable medical device manufacturer in Wheeling, IL is seeking a Senior Process Improvement Engineer who excels in hands-on manufacturing... ...role requires a proactive approach to driving quality and regulatory compliance, making a significant impact on the organization....RegulatoryMedical device
- ...Job Description Job Description Our client is a wellestablished and growing contract manufacturer serving the Aerospace and Medical Device industries. They are hiring a CMM Programmer responsible for developing and writing CMM programs to inspect highprecision...Contract workMedical deviceFull timeTemporary work
- • Develops regulatory strategies for development projects, design changes and manufacturing... ...to ensure successful review by global regulatory authorities. • Directs submission... ...Requirements A minimum of seven years of medical device industry experience with a minimum of...RegulatoryMedical device
- ...Oversee and manage strategic and large vendor contract renewals and support negotiation... ...corrective actions. Ensure vendors comply with regulatory requirements and company policies.... ...Lead, mentor and foster a collaborative global team to deliver vendor management services...Contract workRegulatory
- ICU Medical in Lake Forest, Illinois, is seeking a Regulatory Affairs professional to provide expertise in the registration of medical devices. The role involves supporting the creation of global regulatory strategies, ensuring compliance, and acting as a liaison with regulatory...RegulatoryMedical device
- ...focuses on delivering clinically meaningful software within strict quality and safety standards, coordinating with product owners, regulatory affairs, and cross-functional teams. You will drive design control, traceability, and compliance across the development lifecycle...RegulatoryMedical deviceRemote job
- Overview Senior Process Improvement Engineer | Medical Device Manufacturing Kelly Engineering is partnering with a well-established, FDA... ...FMEA for quality and process issues Support tech transfer and regulatory-driven process changes Improve workflow, layouts, and...RegulatoryMedical device
- ...Industrial Maintenance Mechanic Argon Medical is a global manufacturer of specialty medical... ...Argon offers a broad line of medical devices for Interventional Radiology, Vascular... ...GMP, ISO, FDA, OSHA, EPA, DEP and other regulatory agencies Performs other related duties...RegulatoryMedical deviceApprenticeshipWork experience placementLong distanceDay shift
- ...brilliantly. This role is part of Alcon's Quality & Regulatory Affairs function, ensuring products comply with global, local, and internal regulations while meeting... ...and drive competitive advantage. Support medical device and/or pharmaceutical products, ensuring adherence...RegulatoryMedical deviceLocal area
$60k - $65k
...required. Experience in the pharmaceutical or medical device industry is required. Knowledge of FDA, cGMP, and ICH regulatory standards is required. Strong organizational... ...with salaries ranging from $15.00 to $90,000.00 Global Executive Effectiveness Coordinator - Chicago...RegulatoryMedical deviceFull timePart time
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