Senior Quality Analyst - Complaints & MDR (Medical Devices)
MillenniumSoft Inc
MillenniumSoft Inc is seeking a Quality Analyst for a 10+ months contract in Vernon Hills, IL. The role involves ensuring compliance with quality system standards and managing customer complaints, including investigation and development of corrective actions. Candidates should have a Bachelor’s Degree in Clinical, Science or Engineering and at least 2-3 years of relevant experience. Familiarity with FDA and ISO requirements is preferred. #J-18808-Ljbffr MillenniumSoft Inc
- Position: Quality Analyst - Complaints Management Location: Vernon Hills, IL Duration... ...40.00 1st Shift Client: Medical Device Company Job Category:... ...Level Of Experience: Seniority Level Employment Type: Contract... ...metrics and electronic MDR reports. Development and...ComplaintsMedical deviceContract workH1bWork at officeDay shift
- ...Tech Services | P5 Group is seeking contingent workers in Mundelein, IL to support Medical Device Reporting (MDR) remediation activities. The role involves reviewing historical complaint files for regulatory compliance, preparing MDR submissions, and ensuring adherence...ComplaintsMedical device
- ...across screening, investigation, and MDR submission functions • Establish clear... ...targeted, real-time feedback to drive quality and efficiency • Oversee end-to-end... ...• Minimum of 5 years of experience in medical device complaint handling, MDR reporting, or regulatory...ComplaintsMedical device
- Overview Seeking contingent workers to support Medical Device Reporting (MDR) remediation activities, with a focus on retrospective complaint review reportability assessments under... ...records and work cross‑functionally (Quality, Regulatory, Operations, etc.) to obtain...ComplaintsMedical device
- ...professional to support remediation activities focused on retrospective complaint review reportability assessments under FDA requirements. The... ...at least 1 year of relevant experience, preferably in the medical device or pharmaceutical sectors. Familiarity with complaint...ComplaintsMedical device
$105k - $150.5k
...Summary Provide quality support for ICU Medical Hardware and... ...respect to medical device compliance. Provides... ...closure and escalating to senior management for... ...product review, global complaints, manufacturing quality... ...knowledge of FDA, MDR, and other key medical...SeniorComplaintsMedical deviceWork at office$25 - $30 per hour
...eligibility requirements: medical insurance, dental... ...years of experience in complaint handling, adverse event reporting, MDR evaluation, post-market... ...affairs within the medical device or pharmaceutical industry... ...Form 3500A Experience with quality documentation processes,...ComplaintsMedical deviceTemporary work- ...focus on retrospective complaint review reportability assessments... ...and reassess MDR reportability decisions... ...cross-functionally with Quality, Regulatory, Operations... ...Strong ability to interpret medical narratives, product... ...in a medical device or pharmaceutical environment...ComplaintsMedical device
$35 - $40 per hour
...Title - Supervisor, MDR Remediation Location - Mundelein, IL, 60060 Duration - 06 Months... ...to applicable eligibility requirements: medical insurance, dental insurance, vision... ...Job Description: Experience in medical device complaint handling, MDR reporting, regulatory compliance...ComplaintsMedical deviceTemporary work$38 - $40 per hour
.... Base pay range $38.00/hr - $40.00/hr Job Title: Quality Systems Specialist-Complaints Handling Location: Vernon Hills, IL Hybrid (2 days... ...regulatory requirements. Determine if complaints meet Medical Device Reporting (MDR) criteria and prepare Med Watch reports when...ComplaintsMedical deviceRemote work$113.4k - $186.9k
...research and development efforts of complex medical devices. The role designs, develops and... ...analysis. About You Support Manufacturing, Quality, Regulatory & R&D to ensure systems are... ...and support non‑conforming product and complaint investigations. Education and...SeniorComplaintsMedical deviceCasual workWork at office$25 - $30 per hour
...both new and historical product complaints to assess data completeness and determine MDR reportability. This... ...role will partner closely with Quality, Regulatory Affairs, R&D, and Operations... ...regulatory affairs within the medical device or pharmaceutical industry ~...ComplaintsMedical deviceTemporary work$224k - $280k
...purpose and pride. Your Role at Baxter This Senior Counsel in-house attorney will provide... ...counsel for Baxter International, a medical device and pharmaceutical company based in... ...Arrangements with customers when there are complaints about the performance of a product Best...SeniorComplaintsMedical deviceTemporary workLocal areaWork visaFlexible hours3 days per week$28 - $30 per hour
...eligibility requirements: medical insurance, dental insurance... ...is needed to manage product complaint remediation activities, conduct... ...and ensure timely Medical Device Reporting (MDR) compliance in alignment... ...FDA regulations and internal quality standards. Mission:...ComplaintsMedical deviceHourly payTemporary workRemote workMonday to Friday$62k - $93k
...Medline is seeking an Associate Product Complaints Specialist responsible for managing all aspects of product complaint... ...requires analytical skills and 1+ year experience in Quality, preferably in the Medical Device or Pharma Industry. Key responsibilities include logging...ComplaintsMedical device- ...Your Role at Baxter The Senior Risk Engineer is responsible... ...with engineering, quality, regulatory, clinical, manufacturing... ...issue records, change controls, complaint trends, and NCR/SNCs using... ...progressive experience in medical device risk management or product development...SeniorComplaintsMedical deviceTemporary workLocal areaWork visaFlexible hours
$35 - $40 per hour
...responsible for both product complaint remediation and processing new... ...complaints to determine MDR reportability in alignment with... ...requirements, 21 CFR 803, and Quality System regulations. Review new... ...within a regulated industry. ~ Medical Device Experience Job Type &...ComplaintsMedical deviceContract workTemporary work$35 - $40 per hour
...responsible for both product complaint remediation and processing new... ...complaints to determine MDR reportability in alignment with... ...requirements, 21 CFR 803, and Quality System regulations. Review... ...obligations. Skills 21 CFR 803, Medical Device Reporting, Adverse Event, FDA...ComplaintsMedical deviceContract workTemporary work- LHH is seeking a motivated Quality Control Manager in Buffalo Grove, Illinois. This high-impact managerial role involves overseeing Quality Control laboratory operations in a regulated environment. The successful candidate will lead a team of microbiologists and quality...SeniorMedical device
- A leading medical device company in Vernon Hills is seeking a Sr. R&D Engineer to lead the development of innovative medical devices. You will be responsible for designing and testing new products while ensuring compliance with regulatory standards. The ideal candidate...SeniorMedical device
- ...Hollister Incorporated in Libertyville, IL is seeking a Senior Design Assurance Quality Engineer I-II. This role involves guiding cross-functional teams in design controls for medical devices and facilitating quality activities for new product development. The ideal candidate...SeniorMedical device
$90k - $125k
...Senior Design Assurance Quality Engineer I-II Location: Libertyville, IL, US, 60048-3781 Company: Hollister... ...global regulatory requirements for medical devices Facilitate project quality... ...development Experience with the EU MDD/MDR directives and regulations and ISO 1...SeniorMedical deviceWork at officeWorldwideVisa sponsorship- ...Senior Quality Assurance Engineer (Design Assurance) The Senior Quality Assurance Engineer (Design Assurance) is responsible for providing... ...design transfer, and managing risk documentation across medical device product lines (Class I and Class II 510(k)). The engineer...SeniorMedical device
- A renowned consulting firm is seeking a Quality Systems Specialist to manage customer complaints while ensuring compliance with FDA and ISO regulations. This... ...and experience in quality systems within the medical device or pharmaceutical industry. The position offers a...ComplaintsMedical device
- ...Pty is looking for an Associate Product Complaints Specialist in Mundelein, Illinois. This... ..., and providing support on quality activities. The ideal candidate will have... ...in the quality field, preferably in the medical device or pharma industry. The position offers...ComplaintsMedical device
- ...Regulatory Affairs Level III (Senior Specialist) position... ..., and sales of medical devices (including Class I and... ...approvals, supporting quality management system (QMS... ...documentation for EU MDR compliance International... ...to resolve complex complaints and implement long-...ComplaintsMedical device
$85k - $100k
...and execute processes to ensure product quality. Requires working in a cross‑functional... ...corrective actions. 6. Support complaint sample evaluations and investigations.... ...certification a plus 3+ years’ experience in of Medical Device (21 CFR 820) and/or Drug (21 CFR 210 &...SeniorComplaintsMedical devicePermanent employmentWork experience placement$110k - $130k
...Hiring: Senior EHS Engineer Libertyville Direct Hire | Full Time $110K–$130K + 10% Annual Bonus We are seeking a hands-on Senior EHS Engineer to support the launch of a brand-new medical device manufacturing facility. This person will serve as the site EHS...SeniorMedical deviceFull time$23.25 - $33.75 per hour
...Complaint Remediation Quality Tech The Complaint Remediation Quality Tech is responsible for executing targeted product complaint remediation... ...with 3+ year of experience in Quality within the Medical Device or Pharma Industry OR Bachelor's degree in a relevant field...ComplaintsMedical deviceHourly payMinimum wageWork at officeLocal areaWorldwide$85k - $116.9k
...Quality Engineer Support our extraordinary teams who build great products and contribute... ..., product related CAPA and customer complaint investigations Lead creation and... ...6 years' experience working within the Medical Device industry, with overall working experience...ComplaintsMedical deviceTemporary workWork experience placementVisa sponsorshipFlexible hours
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