Quality Assurance Specialist - Medical Devices & Compliance
Organ Recovery Systems
Organ Recovery Systems, headquartered in Itasca, IL, is a global leader in organ preservation solutions. The Quality Specialist will support the Quality Management System (QMS) to ensure regulatory compliance under FDA QMSR, ISO 13485, ISO 14971, and MDSAP, while supporting product release, complaint handling, internal audits, and CAPA processes. The role emphasizes maintaining document control, continuous monitoring of QMS effectiveness, and collaboration with multiple departments to uphold #J-18808-Ljbffr Organ Recovery Systems
- Organ Recovery Systems in Itasca, IL seeks a Quality Engineer - Device Investigation to coordinate and document investigations of medical devices, including hardware, software,... ...audit-ready records, and support QMS compliance across regulatory requirements. You will...Medical device
- AIT Worldwide Logistics is seeking a Quality Assurance Specialist to support and lead quality management across the organization, ensuring documentation accuracy and training compliance. You will monitor KPIs, support non-conformance investigations, and coordinate audits...SuggestedLocal areaWorldwide
- ...employees who are dedicated to safety and quality. We are a trusted partner to more than... ..., including more than 40 of the top 50 medical device companies and 9 of the top 10... ...workflows that increase efficiency, strengthen compliance, improve data accuracy, and enhance the...Medical deviceFull timeWorldwide
- ...programs, and employment practices while ensuring consistency and compliance. Support employee experience initiatives, site... ...radiopharmaceutical, pharmaceutical, biotechnology, life sciences, medical device, or other highly regulated industries preferred. Demonstrated...Medical deviceWork at officeLocal area
- ...are dedicated to safety and quality. We are a trusted partner to... ...more than 40 of the top 50 medical device companies and 9 of the top 1... ...with site leaders to ensure compliance with federal, state, and local... ..., Engineering, and Quality Assurance to sustain EHSS compliance and...Medical deviceFull timeFor contractorsLocal areaImmediate startWorldwideFlexible hours
- ...About Del Medical, Inc.: Del Medical, Inc. is a leading company in the medical device manufacturing industry. We're looking for a... ...part of a team that values quality, we encourage you to apply.... ...products for traceability and compliance. Keep track of...Medical device
$63.38k - $89.47k
...Quality Assurance Specialist ID 2026-7842 Position Type Regular Full-Time Introduction Join us at AIT, where we... ...applicable policies and procedures, monitoring training compliance, supporting non-conformance support, maintaining quality...Full timeWork experience placementLocal areaWorldwideFlexible hours- ...functional workstreams across Jama Connect, Arena, GitHub, and SOLIDWORKS/PDM. You will own risk integration, verification planning, and evidence readiness, collaborating with R&D, Quality, Regulatory, and manufacturing to deliver compliant, #J-18808-Ljbffr Jobleads-USMedical device
- ...SaMD development Regulatory Assurance: FDA 510(k) support, EU MDR/IVDR compliance, DHF management, IEC 62304, CSV/... ...manufacturing/test support for medical device. Key responsibilities Work... ...product-development, or regulatory/quality services into medical device,...Medical deviceFull time
- ...onboarding and job-specific training for production and quality staff in a medical device manufacturing setting. You will partner with Quality, Manufacturing... ...to build a skilled workforce focused on safety, compliance, and continuous improvement of training programs for...Medical device
- Rauland, a division of AMETEK, seeks a Sr. Manager, Regulatory Affairs to lead the global regulatory function and ensure compliance with FDA, EU MDR, and other international requirements. You will shape regulatory strategy across product development, market access, and...Medical device
- ...to lead global regulatory strategy and ensure compliance across FDA, EU MDR, and international requirements... ...-functional collaboration with Engineering, Quality, and Operations. The role demands 10+ years in medical device regulatory affairs, strong leadership, and travel...Medical device
$135k - $150k
...in highly regulated industries including Medical Devices, Life Sciences, Aerospace & Defense, Industrial Electronics, and other quality-critical markets. The successful candidate... ...'s quality systems and regulatory compliance capabilities. Customer Relationship...Medical deviceFull timeContract work$92k - $149k
...worldwide, we have over 3,000 employees who are dedicated to safety and quality. We are a trusted partner to more than 5,800 customers in over 50 countries, including more than 40 of the top 50 medical device companies and 9 of the top 10 pharmaceutical companies. We’re...Medical deviceContract workTemporary workFor contractorsImmediate startWorldwideFlexible hours$247.4k - $385.4k
...Vice President, Quality Assurance & Regulatory AffairsRegal Rexnord is seeking a senior, business-minded quality, product compliance, and operational excellence leader to serve as Vice... ...defense, FAA-regulated, FAR/DFARS, FDA medical device, medical, data center, or...Medical devicePermanent employment$18.03 - $25.96 per hour
...starting or growing a career in laboratory science, biotechnology, medical devices, or life sciences?We are looking for motivated, detail-... ...provide structured training to help you learn our procedures, quality standards, documentation practices, and testing processes.As...Medical deviceHourly pay- ...able to read and interpret ruler, scales and other measurement devices. While performing the duties of this job, the employee is regularly... ...products, personal care, nutraceutical, pharmaceutical, medical device, and technology industries. With locations across the U....Medical deviceHourly payTemporary work
- Randstad USA in Melrose Park, IL is seeking a QA Documentation Specialist for a full-time, on-site role. The contract is 3-months with... ..., strong Word skills, and a background in pharma/biotech or medical devices. On-site work Monday-Friday, 8:00 AM-5:00 PM. #J-18808-...Medical deviceFull timeContract workMonday to Friday
- ...global regulatory affairs function and ensuring compliance with applicable domestic and international medical device regulations. This role develops and executes regulatory... ...with Engineering, Product Management, Clinical, Quality, and Operations teams to ensure regulatory...Medical device
- ...Responsibilities Regulatory Strategy & Compliance Develop and implement... ...supplements, and Class I medical devices. Interpret and apply... ...with R&D, Marketing, and Quality teams during product... ...Collaborate with Quality Assurance to support audits, inspections...Medical deviceContract work
- ...Kabi USA in Melrose Park, IL seeks a Sr QA Supplier Specialist to support regulatory, ISO and global compliance while ensuring supplier management and internal... ...Approved Vendor List, and supporting regional and global quality agreements. Strong QA/QC background and English...
$20 - $24.5 per hour
...reliable, detail-oriented QA Documentation Specialist for an immediate, full-time on-site... ...Prior pharmaceutical, biotech, or medical device industry background. Direct... ...Good Manufacturing Practices (GMP), Quality Assurance (QA), Batch Record Equal Opportunity...Medical deviceHourly payFull timeContract workTemporary workWork experience placementImmediate startMonday to Friday- Arjo in Roselle, IL seeks a Service Consultant to handle delivery, pickup, maintenance and quality control of medical equipment, ensuring infection control and regulatory compliance. The role requires customer-facing service with strong organizational and problem-solving...Shift workWeekend work
- Meds.com is seeking a meticulous Quality Assurance Specialist for our Elmhurst pharmacy facility to uphold product safety, regulatory compliance, and operational quality across daily compounding and fulfillment. In this role you will audit processes, review batch records...
- ...Opportunity Senior plc is seeking a Director of Trade Compliance – North America to provide strategic and operational compliance... ...background (e.g., aerospace, defense, land vehicles, oil & gas, medical devices) Bilingual English/Spanish preferred Core...Medical devicePermanent employmentTemporary workFor contractorsImmediate startRemote workWorldwideFlexible hours
- ...complexity over the first 12–24 months Contribute to ACME's AS9100 quality system through accurate documentation, revision control, and... ...spindle programming a strong plus) Aerospace, defense, or medical device manufacturing experience — AS9100, NADCAP, or ISO 9001...Medical deviceWork at office
- ...Quality Assurance Specialist Performs routine audits of manufacturing areas to ensure product quality and SOP/GMP compliance at the Melrose Park Manufacturing Facility. Assists in troubleshooting... ...required, Pharmaceutical, Medical Device or Food Industry experience...Medical devicePermanent employmentWork experience placementImmediate start
$17 - $19 per hour
...label inspector machines to include visual quality control. They will operate equipment to... ...interpret ruler, scales and other measurement devices. While performing the duties of this job,... ...care, nutraceutical, pharmaceutical, medical device, and technology industries. With...Medical deviceHourly payTemporary workLocal areaAfternoon shift$19 per hour
...Job Title: Quality Assurance Associate City and State: Elgin, IL Pay Rate: $19/hour Schedule/Shift: 1st Shift – 6:00 AM–4:30 PM, Monday–Thursday... ...assurance or manufacturing experience is a plus Benefits: Medical Plan Dental Plan Vision/Eyewear plan IL Paid Leave Hours 401k...Full timeShift workDay shift$19 per hour
...Quality Control TechnicianMax Pay Rate $19.00 Interviews will be Face to Face or TeamsTemp to Hire Candidates will be on the production... ...and pattern and wet processing to ensure orders are in compliance with corporate/customers' quality requirementsReporting on process...
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