Senior Quality Auditor - Medical Devices Compliance
$86.7k - $173.3kAbbott Laboratories company
Abbott Laboratories is seeking a Senior Quality Auditor for their Lake Forest, IL location to develop and execute audit programs in the Rapid and Molecular Diagnostics Division. The role requires a Bachelor’s degree and at least 8 years of experience, including 3 in quality roles within the medical device industry. Responsibilities include conducting internal audits and supporting compliance with quality system regulations. This position offers a salary range of $86,700.00 – $173,300.00. #J-18808-Ljbffr
$86.7k - $173.3k
...Cerebral Palsy of Georgia is seeking a Senior Quality Auditor to develop and execute the audit... ...least 8 years of experience in the medical device industry and at least 3 years as a Quality... ...role involves performing internal compliance audits and third-party supplier...SeniorMedical device$86.7k - $173.3k
...Employees can qualify for free medical coverage in our Health... ...diseases and other conditions. Senior Quality Auditor is responsible for... ...performance of independent internal compliance audits for RMDx entities (... ...work experience in medical device industry, including...SeniorMedical deviceWork experience placementLocal areaWorldwide- ...issues today and address the medical challenges of tomorrow. We... .... Job Description The Senior Specialist, Quality Systems is responsible for... ...pharmaceutical products, medical devices, combination products, and... ...the final product—are in compliance with corporate and governmental...SeniorMedical deviceTemporary workLocal area
$129.3k - $258.7k
Senior Manager, Strategy Insights and Analytics page is loaded## Senior Manager, Strategy Insights and Analyticslocations: United... ...healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000...SeniorMedical deviceWorldwide- ...responsibilities by providing quality consultation, training,... ...for pharmaceutical products, medical devices, and regulated studies.... ...resolution of quality and regulatory compliance issues. Provide... ...regulations and guidelines to GxP auditors and functional areas personnel...Medical deviceWorldwide
$68.5k - $88.02k
...development while maintaining regulatory information and supporting global registrations. The ideal candidate has 2+ years in Medical Device Regulatory Affairs and strong communication skills. This full-time position offers a competitive salary range between $68,500 and...SeniorMedical deviceRemote jobFull time- A Abbott Laboratories em Lake Forest, IL, está buscando um(a) Principal Molding Engineer para liderar atividades de moldagem e garantir conformidade com padrões de segurança e qualidade. O(a) candidato(a) ideal terá bacharelado em engenharia e mais de cinco anos de experi...SeniorMedical device
- ...Hybrid Senior Manager, Regulatory Affairs Lincolnshire, Illinois... ...worldwide for the finest quality in innovative diagnostic... ...strategy for new and modified medical device products. The Senior Manager... ...materials for accuracy and compliance with regulatory standards....SeniorMedical deviceWork at officeWorldwide
$40 - $43 per hour
...ManpowerGroup Global, Inc. in Lake Forest, IL is seeking a Software Quality Assurance Engineer to ensure regulatory compliance of healthcare products. The role involves defining project goals, providing solutions for quality assurance, and collaborating with various teams...Medical deviceContract work- ...Chicago, IL to prepare and install solutions for regulated devices. You will participate in architecture discussions, develop... ...applications, and work closely with cross-functional teams to ensure quality and compliance. The ideal candidate has extensive experience in software...Medical device
$85k - $128k
...Senior Sox Internal Auditor The Senior SOX Internal Auditor plays a key role in ensuring Medline's compliance with the Sarbanes-Oxley Act (SOX) section 4... ...awareness, and audit quality. Provide value-add... ...healthcare, life sciences, or medical device manufacturing/...SeniorMedical deviceMinimum wageWork experience placementLocal areaWorldwide$92.89k - $176.49k
...! Job Scope The Senior Manager, Supply Chain Planning... ...closely with manufacturing, quality, engineering and sourcing to... ...~2+ Years Experience in a Medical Device, Pharma, or other Healthcare... ...basis of disability. In compliance with federal law, all persons...SeniorMedical deviceOngoing contractWork experience placementWork at officeLocal areaWorldwide$78k - $156k
The Opportunity The Senior Specialist - IT Quality provides quality oversight and compliance leadership for regulated data center facilities, utilities, and equipment... ..., pharmaceutical, biotechnology, or medical device industries, and data center operations, facilities...SeniorMedical deviceWorldwide$102.85k - $133.1k
...eye health. This role is part of Alcon's Quality & Regulatory Affairs function, a... ...responsible for supporting regulatory compliance activities for Alcon's Surgical portfolio... ...strategy execution with a focus on Retina medical devices within the Surgical franchise, partnering...SeniorMedical deviceHourly payLocal areaWorldwideVisa sponsorshipRelocation packageFlexible hours- A global medical device company is seeking a Manager, Engineering - Quality to provide leadership and ensure compliance with quality standards. The successful candidate will manage quality engineering processes, support product development, and ensure alignment with regulatory...Medical deviceFull time
- A renowned consulting firm is seeking a Quality Systems Specialist to manage customer complaints while ensuring compliance with FDA and ISO regulations. This role involves... ...experience in quality systems within the medical device or pharmaceutical industry. The position offers...Medical device
$190k - $380k
...businesses and products in diagnostics, medical devices, nutritionals and branded generic... ...countries. THE OPPORTUNITY: The Senior Director AI Strategy, Governance & Transformation... ...(RAI), risk controls, and regulatory compliance by design. Drive adoption, change...SeniorMedical deviceFull timeWork at office- A medical device engineering company in North Chicago is seeking a mechanical/device engineer with extensive experience in drug delivery... ...CAD design, MoldFlow analysis, and testing of prototypes in compliance with industry standards. Ideal candidates will have 7-12 years...SeniorMedical device
$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... ...Counsel’s primary area of focus will be compliance with U.S. Fraud, Waste & Abuse laws for...SeniorMedical deviceTemporary workLocal areaWork visaFlexible hours3 days per week$149.3k - $298.7k
...businesses and products in diagnostics, medical devices, nutritionals and branded generic... ...people in more than 160 countries. The Senior Counsel, eDiscovery is responsible for... ...management system and follow-up on legal hold compliance and questionnaire responses. Develop...SeniorMedical deviceFull timeContract workFor contractorsWork at officeShift work- ...Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management,... ...an owner’s representative to ensure engineering quality, process integrity, and alignment with...Medical deviceFor contractorsWeekend work
$99.3k - $198.7k
...and products in diagnostics, medical devices, nutritionals and branded generic... ...Abbott location. The Abbott Quality and Regulatory (AQR) Global compliance audit function is a corporate... ...We are seeking an experienced Senior Compliance Auditor with demonstrated expertise in...SeniorMedical deviceFull timeWorldwide- Abbott Laboratories is seeking a Senior Specialist - IT Quality in Waukegan, IL. This onsite role ensures quality oversight and compliance for data center facilities and operations in... ...career development opportunities, free medical coverage, and excellent retirement savings...Senior
$129.3k - $258.7k
...Laboratories is seeking a Head of Commercial Quality US to lead global Quality Management Systems and ensure regulatory compliance. The role requires strong leadership in... ...experience in regulated industries, especially in medical devices or diagnostics, along with project...Medical device- AbbVie is seeking a Device Regulatory Affairs Submission Manager responsible for leading... ...submission of regulatory dossiers for medical devices. The ideal candidate has 6+ years... ...with multiple internal teams to ensure compliance and timelines are met, contributing significantly...Medical device
- Allergan is seeking a Device Regulatory Affairs Submission Manager located in North Chicago. This role leads the planning and submission of regulatory dossiers for medical devices, ensuring compliance with global standards. Candidates should possess a bachelor's degree...Medical device
- ...Sr. Associate II in Regulatory Affairs Strategy to ensure compliance and quality in our Surgical portfolio. This role, based in Lake... ...product submissions and developing regulatory strategies for medical devices. The ideal candidate should have at least 2 years of relevant...Medical device
$84.87k - $98.35k
A medical device company in Gurnee, IL, is looking for a Technical Lead in product development. This role involves leading product development from concept to launch while adhering to established design control processes. The ideal candidate will have a Bachelor's degree...SeniorMedical device$85k - $100k
A global medical device partner is seeking a Quality Engineer II to provide quality support in medical device manufacturing. This technical role involves... ...issues, managing nonconformances, and ensuring compliance with quality regulations. The ideal candidate will have...Medical device- ...company located in Lake Forest, Illinois, is seeking a Senior Pharmaceutical Recruiter. The ideal candidate will provide regulatory support for both U.S. and global medical device submissions, focusing on compliance with FDA and EU requirements. Responsibilities include...Medical device
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