Quality Specialist — Medical Devices & Compliance
$60kDormont Manufacturing Co
Dormont Manufacturing Co, located in Chicago, Illinois, seeks a Quality Specialist responsible for quality control activities of production components. This hybrid role requires ensuring proper specifications and compliance with regulatory standards. The ideal candidate will have a Bachelor's degree or 2 years of experience in the Medical Device or Pharmaceutical industry, with knowledge of ISO 13485. Competitive salary starting at $60,000, along with comprehensive health coverage and flexible benefits, make this an excellent opportunity. #J-18808-Ljbffr Dormont Manufacturing Co
$60k
...What Will You Do? The Overview The Quality Specialist is responsible for supporting production... ...quality inspections of finished goods and device history records, and release goods, if... ...at least 2 years of work experience in Medical Device or Pharmaceutical production...Medical deviceTemporary workWork experience placementWork at officeFlexible hours$25.55 per hour
...unique combination of skill + passion. If you have the qualities and drive to lead yourself or teams, there are roles ready... ...of the distribution center. This position acts in compliance to drug, medical device, and local regulations. Ensures quality processes are maintained...Medical deviceHourly payPermanent employmentFull timeTemporary workWork experience placementLocal areaMonday to FridayFlexible hours- ...Two Australia Pty is seeking a Senior Quality Engineer for their Chicago location. You... ...production processes while ensuring regulatory compliance. The ideal candidate will hold a... ...Engineering, particularly within the medical devices industry. The position offers a hybrid...Medical deviceRemote work
$79k - $119k
Dormont Manufacturing Co in Chicago is seeking a Quality Engineer to independently set quality standards, manage vendor relationships, and ensure compliance with regulations. The ideal candidate will have a Bachelor’s degree in Engineering or related field, along with at...Medical device- ...What Will You Do? The Quality Specialist is responsible for supporting production activities, including... ...inspections of finished goods and device history records, and release goods if... ...salary, performance bonus, and equity. Medical, dental, and vision plans with multiple...Medical deviceTemporary workWork experience placementWork at office
- ...Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in Laboratory, Compliance, Computer, Engineering, Project Management, Validation... ...as an owner’s representative to ensure engineering quality, process integrity, and alignment with operational requirements...Medical deviceFor contractors
- ...Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management,... ...Ensure adherence to scope, schedule, cost, and quality objectives. Manage project execution to support...Medical deviceWeekend work
$63k - $95k
...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... .... The Regulatory Affairs Specialist supports the regulatory strategy... ..., and ensures ongoing compliance with global regulatory bodies...Medical deviceFor contractorsImmediate startWorldwideFlexible hours$15.75 - $16.25 per hour
...informed capital decisions. Our programs support 100% regulatory compliance and drives 98% equipment uptime—so clinicians can focus on... ...-integrated outpatient clinics. With more than 1.15 million medical devices managed, we provide the clarity and consistency needed in...Medical deviceFor contractorsApprenticeshipInternshipLocal areaRemote workFlexible hours- ...policies, and procedures that comply with FDA Quality System Regulations (QSR), ISO 13485, and... ...with preferably a minimum of 3 years of medical sales experience in ophthalmology, with a... ...sales track record in the medical device industry ~ Ability to navigate complex...Medical deviceFull timeNight shift
- ...Coding Quality Auditor And Specialist, Hb Coding, Full-time, Days (Remote - Must Reside In Il, In, Ia,... ...organization's Code of Ethics and Corporate Compliance Program, and complies with all... ...educator to clinical teams and medical staff Identifies strategic plans...Remote jobFull timeLocal areaRelocation package
- ...while building strong relationships with healthcare professionals. Applicants should have a Bachelor’s degree and 3-5 years of medical device sales experience, along with a strong understanding of the healthcare system. This role requires excellent communication skills...Medical device
- ...Key Account Executive Step into a high-impact role where you sit at the center of innovation for leading medical device and bioprocess manufacturers. As a Key Account Executive, you will become a trusted partner to strategic customers, shaping how critical components...Medical device
- A healthcare institution is seeking a Coding Quality Auditor and Specialist to ensure compliance in clinical documentation and coding. This remote position requires strong analytical skills and certifications in coding. Responsibilities include collaborating with clinical...Remote job
$110k - $155k
Tempus AI, Inc. is seeking a Lead Quality Engineer to join its multidisciplinary team in Chicago. This... ...implementing quality assurance for the development of IVD medical devices and LDT products while overseeing regulatory compliance for Class 3 FDA and EU IVDR standards. The...Medical device$185k - $215k
Tempus, Inc. is seeking a Sr. Manager, Medical Device Cyber Security in Chicago. This role involves owning the medical device cyber security... ...integrate security into the device lifecycle, and ensuring compliance with regulatory guidelines. Candidates should have over 7...Medical device$154k - $231k
Medline seeks a Quality Director in Chicago to guide the quality assurance of medical device products. This role includes leading teams to ensure compliance with regulations, developing product specifications, and managing relationships with suppliers and manufacturing...Medical device$110k - $150k
Dormont Manufacturing Co is seeking a Manager of Regulatory Affairs to lead the development of global regulatory strategies for medical devices. This role involves close collaboration with scientists, engineers, and legal teams to successfully gain marketing...Medical device$60k - $70k
Sol-Millennium Medical Group is seeking a detail-oriented Sales Operations Specialist to join our North America team in Chicago. This operational and customer-facing... ...lifecycle, communicate with stakeholders, and ensure compliance with industry standards. A Bachelor’s degree...Medical device- ...seeks a Regulatory Affairs Level III (Senior Specialist) to manage global product registrations and ensure compliance in the medical device sector. The role involves developing... ...leading 510(k) submissions, and supporting quality management systems. Ideal candidates have...Medical device
- ...looking for a Regulatory and Clinical Specialist to support clinical evaluation activities... ...submissions for active implantable medical devices. This role involves authoring clinical... ...conducting literature searches, and ensuring compliance with EU and FDA regulations. The ideal...Medical deviceRemote job
- ...Regulatory Affairs Level III (Senior Specialist) position is responsible for... ...and ensuring regulatory compliance in the design, manufacturing, and sales of medical devices (including Class I and II devices... ...approvals, supporting quality management system (QMS) objectives...Medical device
- ...managing sales tactics, clinician training, and expanding key relationships. Qualified candidates should have at least 3 years of medical device sales experience, possess a Bachelor's degree, and be able to travel up to 50%. The team is passionate and focused on...Medical device
- Medline Industries, LP is seeking a Quality Manager to provide leadership and direction... ...developing strategies to ensure compliance with regulatory standards and delivering... ...7 years of relevant experience in the medical device industry, including 4 years in management...Medical device
- ...Job Summary: Quality Engineer / Quality Compliance Engineer with experience supporting remediation efforts and maintaining quality standards within regulated medical device, pharmaceutical, OTC drug, and cosmetic environments. Responsible for supporting Quality...Medical device
- ...candidates for a hybrid role focusing on the validation of software supporting medical devices. Located in Chicago, New York, or Redwood City, this position involves risk assessments, regulatory compliance, and cross-functional collaboration. The ideal applicant possesses a BA...Medical device
$1,300 per day
...Pharma Quality Auditor For nearly 30 years, SQA Services has been a leading provider of managed supplier quality services, offering... ...supply chains of various clients within the pharmaceutical, medical device, cosmetics, biologics, and/or animal health industries...Medical deviceContract workLocal areaRemote workWorldwide- ...Services North America, Inc is seeking a Quality Systems Associate based in Maywood, IL.... ...training functions under supervision to ensure compliance with regulations. Key responsibilities... ...compliance is crucial. Benefits include medical, dental, vision, and participation in a...
- ...s Hospital of Chicago is seeking a Quality Assurance & Education Specialist to conduct performance audits and facilitate... ...processes through training and compliance audits. Candidates must have at... ...school diploma. Benefits include medical, dental, and vision insurance, along...
$60k - $70k
SOL-MILLENNIUM Medical Group is a global healthcare company dedicated... ..., and distributing high-quality medical devices. Our products protect... ...-oriented Sales Operations Specialist to join our North America team... ..., accurate invoicing, and compliance with industry standards. You...Medical deviceWork at office
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