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
- 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
- ...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
$20 - $30 per hour
...~5+ years of experience in complaint handling, adverse event reporting, MDR evaluation, post-market surveillance... ...or regulatory affairs within the medical device or pharmaceutical industry ~ Strong... ...collaborate effectively across Quality, Regulatory Affairs, R&D, and Operations...ComplaintsMedical deviceTemporary work$30 - $32 per hour
...Quality Auditor Location: Mundelein, IL (Hybrid: Tues–Thurs onsite... ..., and compliance of product complaint documentation in a regulated... ...Auditing experience in medical device, pharmaceutical, or healthcare... ...Medical Device Reporting (MDR) audit experience Knowledge...ComplaintsMedical deviceContract workTemporary workRemote work- ...both new and historical product complaints to assess data completeness and determine MDR reportability. This individual... ...role will partner closely with Quality, Regulatory Affairs, R&D, and Operations... ...regulatory affairs within the medical device or pharmaceutical industry...ComplaintsMedical deviceTemporary work
- ...Title: Quality Auditor Schedule: Hybrid (3x onsite) Duration: 3-6... ...completeness, and compliance of product complaint documentation by conducting... ...experience within the medical device, pharmaceutical, or... ...auditing Medical Device Reporting (MDR) documentation Knowledge of complaint...ComplaintsMedical deviceContract workTemporary 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$140k - $191k
...single-use disposable medical products. This role drives... ...teams including R&D, Quality, Regulatory Affairs, Clinical... ...use disposable medical devices. Provide leadership for... ...Device Regulation (MDR) ISO 13485 IEC 62366 (... ...-market surveillance, complaint investigations, and continuous...ComplaintsMedical deviceWork experience placementWork at officeWorldwide- 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
- Medline Industries in Mundelein, Illinois, is seeking a Complaint Remediation Quality Tech responsible for executing targeted product complaint... ...or several years of experience in quality within the medical device or pharmaceutical industry and possess strong analytical...ComplaintsMedical 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
$86.7k - $173.3k
...businesses and products in diagnostics, medical devices, nutritionals and branded generic... ...Molecular Diagnostics Division (RMDx). The Senior Quality Auditor is responsible for developing and... ..., ISO 13485, MDSAP, cGMP Regulations, MDR and IVDR and other regulations and standards...SeniorMedical deviceWork experience placementLocal areaWorldwide$85k - $110k
...for the very finest in quality, innovative diagnostic... ...team (includes Senior Management) of progress... ...gaps, product issues, complaints, and recommend potential... ...of health care plan (medical, vision, and dental insurance... ..., IT or Medical Device. PMP certification preferred...ComplaintsMedical deviceWorldwide$23.25 - $33.75 per hour
Job SummaryThe Complaint Remediation Quality Tech is responsible for executing targeted product complaint remediation activities forMedline. This... ...with 3+ year of experience in Quality within the Medical Device or Pharma Industry OR Bachelor’s degree in a relevant field...ComplaintsMedical deviceMinimum wageWork at officeLocal areaWorldwide$62k - $93k
Job Summary The Assoc Product Complaints Specialist role is responsible for executing all... ...guidance to stakeholders on additional quality activities related to complaints. Responsibilities... ...in Quality, preferably within the Medical Device or Pharma Industry OR Bachelor’s degree...ComplaintsMedical deviceMinimum wageWork experience placementWork at officeLocal area$86.7k - $173.3k
...Senior Quality Auditor This position works out of our Lake Forest, IL location in the Rapid... ...least 3 years in Quality work within the medical device industry, experience as a Quality Systems... ...including QSR, ISO 13485, MDSAP, cGMP, MDR, IVDR and related regulations and...SeniorMedical deviceLocal area- ...Description Title: R&D Senior Engineer Location:... ...Us Founded in 1996, Medical Murray is a privately owned medical device company specializing in... ...with the highest level of quality. What You'll Do... ...requirements. Support customer complaints and investigations as...SeniorComplaintsMedical devicePermanent employmentFull timeTemporary workWork at officeWorldwide
- ...Your Role at Baxter The Senior Risk Engineer is responsible... ...collaborates with engineering, quality, regulatory, clinical,... ...issue records, change controls, complaint trends, and NCR/SNCs using appropriate... ...progressive experience in medical device risk management or product...SeniorComplaintsMedical deviceTemporary workLocal areaWork visaFlexible hours
$124.74k - $161.43k
...Summary The primary objective of the Senior Product Manager role is to meet or exceed... ...(KOLs) and Key Accounts (KAs) in the medical community -related to product areas of focus... ...Graduate / Advanced degree preferred Medical device product marketing experience preferred...SeniorMedical deviceTemporary workFor contractorsWork at officeLocal area- AbbVie is seeking to enhance its Global Quality Organization by handling pharmaceutical, medical device, and combination product complaints. The role focuses on implementing and maintaining the Quality System, ensuring compliance with policies and regulations, and coordinating...ComplaintsMedical device
- ...Division Chief Financial Officer & Senior Director of Finance About the Company Industry leading provider of medical devices & transformative healthcare innovations Industry Medical Device Type Public Company Founded 1931 Employees...SeniorMedical device
$129.3k - $258.7k
...businesses and products in diagnostics, medical devices, nutritionals and branded generic... ...constantly working to deliver the highest quality products and unwavering support to our... ...and analyze glucose levels. As a Senior Engineering Manager , you will Oversee...SeniorMedical deviceFor contractorsWork experience placementWorldwideShift work- A medical device engineering company in North Chicago is seeking a mechanical/device engineer with extensive experience in drug delivery and device design. The candidate will be responsible for 3-D CAD design, MoldFlow analysis, and testing of prototypes in compliance...SeniorMedical device
$106 - $114 per hour
TekWissen ® is seeking a quality lead for New Product Introduction in North Chicago. The role involves ensuring compliance with regulations... ...team members, and driving quality assurance initiatives for medical devices. Applicants should have a Bachelor's Degree in Engineering or...SeniorMedical deviceHourly pay- 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...SeniorMedical device
- ...Illinois, is seeking a candidate to support remediation activities under FDA requirements. This role involves reviewing historical complaint files, applying current FDA definitions, and preparing MDRs when necessary. The ideal candidate will have experience in complaint...Complaints
- ...helping people see brilliantly. This role is part of Alcon's Quality & Regulatory Affairs function, ensuring products comply with... ...maintain compliance and drive competitive advantage. Support medical device and/or pharmaceutical products, ensuring adherence to relevant...SeniorMedical deviceLocal area
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