Canada Regulatory Affairs Lead - Medical Devices Submissions
$75k - $90kMedix™
A leading healthcare consultancy is seeking a Regulatory Affairs Project Lead in Buffalo Grove, IL. The role involves managing regulatory submissions and collaborating with various teams to ensure compliance, particularly in the Canadian market. Candidates should have experience with FDA and Health Canada processes, a valid US passport, and strong organizational skills. This position offers a direct hire employment with a salary range of $75,000-$90,000, onsite from Monday to Friday. #J-18808-Ljbffr Medix™
$96k - $140k
...Libertyville Department : Finance Summary The Lead Financial Analyst serves as a strategic financial advisor and... ...or Master's degree in Finance preferred. Experience in the medical device industry preferred. Deep expertise with Microsoft Excel, Power...Medical deviceWork at officeLocal areaWorldwideVisa sponsorshipNight shift- ...support for remediation efforts. You'll be responsible for maintaining quality standards across medical device, commodity, OTC drug, and cosmetic products. This involves leading investigations into non-conformances, ensuring compliance with regulations, and conducting...Medical device
- 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...Medical device
- A leading engineering firm is looking for an experienced Environmental, Health & Safety (EHS) Engineer to serve as the site’s primary... ...EHS experience in manufacturing and a strong grasp of regulatory requirements, notably OSHA standards. Full-time position with...Medical deviceFull time
$75k - $90k
Regulatory Affairs Project Lead - 247670 Our client is seeking a Regulatory Affairs Project Lead whose... ...Serve as LTD back‑up contact for submissions, registrations, and listings... ...submissions to the FDA and Health Canada for medical devices Conduct predicate searches for substantial...Medical deviceMonday to Friday- ...detail-oriented, experienced Regulatory Affairs Consultant to join our team... ...market access (FDA, Health Canada, EU MDR, and other... ...maintaining documentation for 510(k) submissions, Technical Files, and... ...ISO 13485, and international medical device requirements Reviewing labeling...Medical deviceContract workRemote work
$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...Medical device- Medix is seeking a Quality Lead (255032) in Vernon Hills, Illinois, to lead on the production floor within a medical device manufacturing environment. This hands-on leadership role emphasizes real-time decision making, and ensuring products meet FDA and ISO 13485 standards...Medical device
$25 - $30 per hour
Quality Lead (255032) Vernon Hills, Illinois Salary: USD25 - USD30 per hour + See details in Job Description This is a hands‑on quality leadership role within a medical device manufacturing environment. The QC Floor Lead oversees daily quality control activities on the...Medical deviceHourly pay$100k - $120k
Antylia Scientific is seeking a Payroll Manager in Vernon Hills, IL to oversee the payroll function. This hybrid position involves managing payroll processing for multiple states and ensuring compliance with regulations. Candidates should have over 7 years of experience...- ...A leading pharmaceutical company located in Lake Forest, Illinois,... ...ideal candidate will provide regulatory support for both U.S. and global medical device submissions, focusing on compliance with FDA... ...years of experience in Regulatory Affairs within the medical device...Medical device
- • Develops regulatory strategies for development projects,... ...authorities. • Directs submission related activities by leading the team and motivating... ...minimum of seven years of medical device industry experience with... ...five years in regulatory affairs with direct experience and...Medical device
- RICHARD WOLF MEDICAL INSTRUMENTS CORPORATION is seeking a Quality Control Inspector in Vernon... ...inspections and compliance with regulatory requirements. The ideal candidate should... ...in quality assurance within the medical device industry and be proficient with testing...Medical deviceFull time
- 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...Medical deviceContract work
- ...manage CME grant-funded educational programs. Candidates will develop relationships with supporters in the pharmaceutical and medical device industries, and set revenue goals for contributions. Successful applicants will have a bachelor’s degree and at least four years...Medical device
- ...validation lifecycle from writing protocols to maintaining compliance. This role has a direct impact on quality and regulatory standards within a growing medical device company. Key responsibilities include managing validation protocols and the calibration system,...Medical deviceFull time
- Nemera, a leading firm in drug delivery devices, seeks a Quality Validation Engineer in the United States to plan, coordinate and manage projects ensuring... ...across departments to optimize product quality and regulatory compliance. Responsibilities include coordinating...Medical device
- ...industry. We are seeking an experienced Regulatory Affairs Manager to lead a diverse portfolio of FDA... ...dietary supplements, and Class 1 medical devices. The ideal candidate will possess... ...Review Regulatory Documentation and Submissions Quality & Risk Management Cross Functional...Medical device
- MillenniumSoft Inc is looking for a Marketing Leader in Vernon Hills, IL, to drive marketing initiatives for IV set products, including gravity and extension IV sets. The ideal candidate will have extensive managerial and marketing experience, showcasing excellent communication...Medical deviceContract work
- ...Consultants, Inc. is seeking an experienced Regulatory Affairs Manager to lead a diverse portfolio of FDA-... ...dietary supplements, and Class I medical devices. You will provide regulatory... ...labeling and ingredients, coordinate submissions, and partner with R&D, Marketing and...Medical device
$21.08 - $31.62 per hour
...Department to include; decontamination, instrument set assembly, medical device processing, patient-care equipment processing, case cart... ...procedural area) Preferred: Two (2) years' experience as a lead or experience in staff education Skills: Proficiency in Outlook...Medical deviceHourly payFor contractorsReliefAll shiftsShift workNight shiftWeekend workDay shiftAfternoon shift- ...validate new equipment and processes, assess changes, and improve product realization practices. The role requires 5-7 years in medical device QA/Validation, strong knowledge of 21 CFR 820, ISO 13485, and problem-solving leadership. #J-18808-Ljbffr Sysmex America, Inc.Medical device
$95k - $120k
.... About Us: Vantedge Medical is the premier metals-based med... ...improve product quality. Lead the implementation of Lean... ...comply with industry standards, regulatory requirements, and safety... ...precision machining or medical device industry. Demonstrated expertise...Medical devicePermanent employmentFull time- Lead Auditor - GMP Quality Audits will perform high level assessments of quality... ...detailed and timely manner. Specific Regulatory Standard(s) Competency are a focus including... ...210 Nutritional Supplements: 21CFR111 Medical/Homecare Devices: 21CFR820 Cosmetics: ISO22716...Medical deviceTraineeship
- ...based in Vernon Hills, IL. This 6+ month contract role involves managing change control, documentation, and training systems for medical devices. The ideal candidate will have a high school diploma and two years of relevant experience in a regulated environment....Medical deviceContract work
- MillenniumSoft Inc is seeking a Sr. Quality Engineer to support V. Mueller Platform Quality in Vernon Hills, IL. This contract position is focused on addressing gaps in product specifications and supporting the Quality System across various departments. Candidates should...Medical deviceContract work
$95k - $120k
A medical technology company in Wheeling, Illinois, is seeking a Continuous Improvement Engineer to enhance manufacturing efficiency and... ...20K, reflecting the importance of continuous improvement in the medical device manufacturing sector. #J-18808-Ljbffr Vantedge MedicalMedical deviceFull time- MillenniumSoft Inc is looking for a Quoting & Pricing Specialist in Vernon Hills, IL to support the MMS Infusion business in the medical devices industry. The role involves generating quotes and managing sales contracts while collaborating closely with the sales team. The...Medical deviceContract workWork at office
$21.08 - $31.62 per hour
...Department to include; decontamination, instrument set assembly, medical device processing, patient-care equipment processing, case cart... ...procedural area) Preferred: Two (2) years' experience as a lead or experience in staff education Skills: Proficiency in Outlook...Medical deviceHourly payFull timePart timeFor contractorsReliefAll shiftsShift workNight shiftWeekend workDay shiftAfternoon shift- MillenniumSoft Inc is seeking a Packaging Engineer in Vernon Hills, IL. The successful candidate will have 4-5 years of medical device packaging experience, alongside a degree in Packaging or a related field. The role involves designing and qualifying packaging concepts...Medical deviceContract work
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