QA Investigator: Medical Device Complaints & Lab Compliance
Spectraforce Technologies Inc
Spectraforce Technologies, Inc. is seeking a Quality Assurance (QA) Specialist I to support product complaint documentation, investigations, and data summarization in North Chicago, IL. This 6-month assignment focuses on determining testing steps and ensuring compliant documentation within GMP/GLP frameworks. The ideal candidate has a science/tech background, lab experience, strong communication, and the ability to manage multiple tasks with Agile practices to support QA lab processes and #J-18808-Ljbffr
- ...and Regulatory Affairs (QA/RA) to support our expanding... ...artwork and labeling compliance, customer complaints, supplier qualifications,... ...Support customer complaint investigations, nonconforming product evaluations... ...of ISO 13485, FDA medical device regulations, cGMP, and...ComplaintsMedical deviceFull timeWork at office
$20 - $23 per hour
...QA Recall Coordinator Location: Mundelein, IL Duration: 6 Months to... ...requests are handled efficiently and in compliance with quality and regulatory... ...candidate will have a background in MedTech/medical devices, Quality, complaints, recalls, or field actions. Zendesk...ComplaintsMedical deviceHourly payTemporary work- ...n This is an execution role, not a compliance desk job. You'll own manufacturing quality... ..., and own field quality and complaint investigation. \n \n You'll report directly to... ...\n \n ~10+ years of progressive medical device quality operations experience, with...ComplaintsMedical deviceContract workImmediate startWorldwide
- Medline Industries, a leading medical device company, seeks a Clinical Product Surveillance... ...with active RN licensure to investigate post-market complaints and support clinical safety... ..., supporting safe product use and compliance with regulations. #J-18808-Ljbffr...ComplaintsMedical device
$165k - $230k
...Director, Global Quality and Compliance Excellence BioSpace - AbbVie... ...issues today and address the medical challenges of tomorrow. We strive... ...Site leadership, Quality Lab leadership, global functional... ...combination products, medical devices, tissue, and cosmetics for future...Medical deviceFull timeTemporary workLocal area$78k - $156k
...products in diagnostics, medical devices, nutritionals and... ...instruments, providing lab results for millions... ...for meeting the compliance requirements for Medical... ...On ~ Review medical complaints and potentially reportable... ...and ~ Complaint Investigations Group) to gather...ComplaintsMedical deviceFull timeWorldwideShift work- ...Job Summary The QA Senior Specialist will provide quality assurance support for... .... Proactively identify project and compliance risks and implement appropriate risk assessments... ...the pharmaceutical, biotechnology, medical device, or related regulated industry. ~...Medical deviceFor contractors
- ...Job Description QA Associate/Specialist | Medical Devices | Maryland \n \n X4 Life Sciences... ...of quality and regulatory compliance across the U.S. and... ...Helping manage customer complaints, nonconformances and CAPAs, from investigation through to closure \n Supporting...ComplaintsMedical deviceImmediate start
- ...Responsibilities Develop and execute R&D QA transformation roadmap including... ...functional initiatives in pharmaceutical, medical device, clinical, or quality environments ~ Proficiency... ...~ Understanding of quality systems, compliance expectations, and change management in...Medical device
$95k
...standards. This role leads QA associates, manages monitoring... ...programs, supports timely investigation and resolution of quality issues... ...incidents, and customer complaints. This includes completion of... ...Conducts internal audits to ensure compliance with FSMA, SQF, USDA and FDA...Complaints- ...seeking a senior Quality leader to direct quality teams and ensure compliance across products and processes. You will translate strategic... ...knowledge of QSR/GMP/ISO standards, extensive experience in medical-device environments, and strong leadership for multi-department...Medical device
$96.5k - $183.5k
...issues today and address the medical challenges of tomorrow. We strive... ...is not a software testing or QA engineering role. This bridges... ...role calls for a quality and compliance professional who is deeply technology... ...(pharmaceutical, medical device, or similar)Fluency with...Medical deviceTemporary workWork at officeLocal areaImmediate startRemote workMonday to Friday- ...issues today and address the medical challenges of tomorrow. We strive... ...products and medical devices. Act as the primary interface... ...& Logistics, Marketing & BD, QA, Regulatory, MNO, AbbVie manufacturing... ...assigned accounts, including compliance, regulatory updates, capacity...Medical deviceContract workLocal areaWorldwide
- ...extension of Client’s Medical Affairs organization,... ...disease thought leaders and investigator discussions. \n \n... ...position will include compliance, regulatory and study... ...of concern or product complaints in accordance with... ...diagnostics, and medical device fields have turned to...ComplaintsMedical deviceFull timeTemporary workFor contractorsWork at officeLocal areaWork from homeNight shift1 day per week
$18 - $20 per hour
...tools? We're looking for a Quality Inspector to join a medical device manufacturing operation where quality, accuracy, and attention... ...do not meet specifications. Supporting NCRs, CAPAs, complaint investigations, and root cause analysis . Partnering with Production...ComplaintsMedical deviceHourly payTemporary workLocal area$23 per hour
...and documentation management to ensure compliance with internal requirements and... ...process deviations, procedure deviations, complaints, regulatory audits, customer audits, and... ...experience in inspection, quality assurance, medical device, pharmaceutical, healthcare, or...ComplaintsMedical devicePermanent employmentFull timeContract workTemporary workWork at office- ...Medical Reviewer/Safety Reviewer IIIAre you a licensed RN with specialized expertise in medical device risk management and post-market surveillance?... ...gatekeeper role in evaluating complaint reports, handling medical assessments, and ensuring compliance with global safety...ComplaintsMedical deviceContract workRemote work
- ...health issues today and address the medical challenges of tomorrow. We... ...data integrity, foster regulatory compliance, and contribute to the overall success of drug/device development programs. The Associate... ...about improving how R&D QA operates through data-driven decision...Medical deviceFull timeLocal area
- ...Engineering - Neurosurgery - 3686014 \n \n Join an innovative medical device company seeking a Senior Quality Manager to take ownership of... ...release activities, and quality records. \n Oversee complaint handling, vigilance activities, MDR reporting, and post-market...ComplaintsMedical deviceContract work
$86.7k - $173.3k
...Lake Forest, Illinois. This role develops and executes internal compliance audit programs for diagnostics entities and suppliers,... ...equivalent Minimum 8 years experience with at least 3 years in medical device quality Demonstrated experience as a Quality Systems...Medical device- ...with a focus on retrospective complaint review reportability... ...identifies reportable events. Support compliance with FDA Quality System... ...Strong ability to interpret medical narratives, product information... ...remediation experience in a medical device or pharmaceutical environment...ComplaintsMedical device
- ...a subsection of our Quality Management System such as device master records, customer complaints, product holds, recalls, or incoming quality. You will... ...collaborate with cross-functional teams to ensure FDA/ISO compliance, track progress, review documentation #J-18808-Ljbffr...Complaints
$54k - $82.5k
...leading global provider of mission-critical sterilization and lab testing and advisory services for the healthcare industry. With... ...in over 50 countries, including more than 40 of the top 50 medical device companies and 9 of the top 10 pharmaceutical companies.Reporting...Medical deviceHourly payFor contractorsImmediate startWorldwideFlexible hours$160k - $200k
..., Regulatory Affairs & Compliance FLSA Status: Exempt Reports... ...As needed Department: QA Position Summary... ...letters, or consumer/legal complaints related to labeling or... ...(e.g., label reviews, lab invoice audits, and... ...Additionally, we offer medical, prescription drug plans...ComplaintsContract workTemporary workFlexible hoursShift work- ...health issues today and address the medical challenges of tomorrow. We... ...for adequacy, consistency, and compliance Maintain the audit schedule Represent RD QA for Dossier Program related meetings... ...’ experience in the Medical Device or Pharmaceutical industry, ~...Medical deviceFull timeLocal area
$149.3k - $298.7k
...can grow the career you dream of Free medical coverage for employees* via the Health... ...delivering breakthrough diagnostics, medical devices, nutrition, and medicines that improve... ..., and acquisition decisions. Ensure compliance with Abbott policies, quality standards,...Medical deviceWorldwide- ...across drug substance, drug product, and device or combination products is highly valued... ...and CAPA management, change control, complaint handling, training, and vendor/supplier... ...\n Preferred \n • Experience with medical device or combination product quality systems...ComplaintsMedical deviceFor contractors
$126k - $175k
...regulatory agencies regarding device information or issues. Includes... ...and ongoing activities for compliance with FDA, Health Canada and other... ...rules including those for medical devices products. 7. Manages &... ...Motivated individual with hands‑on RA/QA experience, excellent...Medical deviceWork at officeWorldwide- ...is seeking a Clinical Product Surveillance Specialist to investigate post-market complaints, ensure regulatory reporting, and support product safety... ...of contributing to adverse event evaluations and CAPA processes within a global medical products #J-18808-LjbffrComplaints
- ...a Principal Regulatory Affairs Specialist (Medical Events) to oversee timely review, documentation, and filing of Medical Device Reports including international vigilance for... ...division's products. You will ensure compliance with MDR regulations and support cross-functional...Medical device
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