• Aequor (Thousand Oaks, CA)
    …equivalent combination of education and/or experience. Typically 2 plus years of related quality assurance or manufacturing experience in a GMP pharmaceutical or ... medical device industry. Evaluate documentation and operation according to company guidelines. Be self motivated, attentive to details and able to prioritize and… more
    HireLifeScience (12/02/25)
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  • Twist BioScience (South San Francisco, CA)
    …in a GMP, Biotechnology, Pharmaceuticals or another Regulated Industry.Experience in Quality Assurance /Regulatory requirements in medical devices, IVD, ... interact with individuals at multiple levels within all functional departments, including Quality Assurance , Regulatory Affairs, Supplier Quality , Supply… more
    HireLifeScience (12/06/25)
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  • Insmed Incorporated (NJ)
    …engaged and aligned with project goals including Manufacturing, Analytical Development, Quality Assurance , and Regulatory, with input from Commercial, Research, ... preference for 5+ years of project management experience in the pharmaceutical, medical device , or related industry.Ability to influence outcomes without direct… more
    HireLifeScience (09/09/25)
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  • Unknown (Guilford, CT)
    President About the Company Respected biomedical device company Industry Medical Device Type Privately Held About the Role The Company is in search of a ... of quality , innovation, and customer focus, particularly in the competitive medical device industry. The President will also be tasked with overseeing… more
    job goal (12/05/25)
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  • Unknown (Tempe, AZ)
    …a minimum of 10 years' experience in product development, with a focus on aortic medical device development. The role requires a strong track record in leading ... management skills, and a deep understanding of regulatory requirements and quality assurance standards. The ideal candidate will be a strategic thinker with… more
    job goal (12/05/25)
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  • Quality Assurance Manager…

    Jabil (St. Petersburg, FL)
    …and equipment as applied to new or existing products. Conducts quality assurance testing as appropriate.ESSENTIAL DUTIES AND RESPONSIBILITIES. Provides ... improvements. Reports to management as necessary and required on the status of quality assurance programs and practices.. Manages compliance all site required… more
    Jabil (10/25/25)
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  • Staff Design & Reliability Assurance

    Integra LifeSciences (Mansfield, MA)
    …knowledge of DFSS techniques * 8 years of experience in a Quality Assurance role for medical device or pharmaceutical product development * Fluent ... new standards of care. This **Staff Design & Reliability Assurance Quality Engineer** is a key functional...Risk Management (ISO 14971 2019), MDD ( Medical Device Directive), IEC 62366, ISO 13485 ( Quality more
    Integra LifeSciences (11/12/25)
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  • Quality Assurance Manager

    Danaher Corporation (Waltham, MA)
    …or a related field. + Experience: Minimum of 5 years in quality assurance within the medical device or related industry. + Leadership Experience: ... agile and above all audacious so we can truly drive science forward. The Quality Assurance Manager is responsible for overseeing an ISO 9001 certified … more
    Danaher Corporation (11/11/25)
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  • Associate Manager, Medical Device

    Regeneron Pharmaceuticals (East Greenbush, NY)
    We are currently looking to fill a Manager, Medical Device Quality Assurance position on our Medical Device Sustaining Engineering QA team. This ... quality risk management principles and their application to medical device development and commercialization. The scope...applications of Quality Assurance and Quality Risk Management in the medical more
    Regeneron Pharmaceuticals (10/17/25)
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  • Quality Engineer II - Design & Reliability…

    Integra LifeSciences (Braintree, MA)
    …Mechanical) or related discipline, with 3+ years of experience in Quality Assurance role for medical device or pharmaceutical manufacturing, or ... treatment pathways to advance patient outcomes and set new standards of care. The Quality Design and Reliability Assurance (DRA) Engineer II is responsible for… more
    Integra LifeSciences (12/06/25)
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  • Quality Engineer

    Actalent (Watertown, CT)
    …repeatability of the results. Essential Skills + Quality engineering + Quality assurance + Audit + Medical device expertise + CMM programming + GD&T ... Job Title: Quality Engineer For immediate consideration, please email resume...all testing processes and product developments comply with relevant medical device regulations such as FDA (21… more
    Actalent (12/04/25)
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  • Senior Quality Engineer I - Validations,…

    Integra LifeSciences (Plainsboro, NJ)
    …preferred + Experience: 6 to 8 years of experience in a Quality Assurance role for medical device or pharmaceutical manufacturing. + Demonstrates ... and Drug Administration regulations, ISO 9001, ISO 13485, the Medical Device Directive, the Canadian Medical...and surveillance audits and customer audits. + Perform other Quality Assurance and Quality Engineering… more
    Integra LifeSciences (10/08/25)
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  • Quality Assurance Manager

    GE HealthCare (Cleveland, OH)
    …**Desired Characteristics:** + Experience in Quality Assurance or Quality Engineering within the Medical Device or Pharmaceutical industry, ... 7 years of relevant experience in Quality Assurance in a regulated industry, either Medical ... Device (SaMD) + Demonstrated understanding of Medical Device Quality Management System… more
    GE HealthCare (10/04/25)
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  • Senior Pharma QA Engineer

    System One (Redmond, WA)
    …field or a related field + 1-3 years of experience in quality assurance + Medical Device experience is highly preferred Benefits System One ... $46.66- $53.00 Type: Contract Overview Global Medical Device company looking to hire experienced Quality Assurance Engineer to join their growing team.… more
    System One (11/26/25)
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  • QA Specialist

    Envista Holdings Corporation (Quakertown, PA)
    …+ High school diploma or equivalent plus 3 years of experience working in a quality assurance , medical device and/or manufacturing setting or associate ... quality backgrounds that work collaboratively in the fast-paced medical device field. A friendly and open...and Quality Systems in a regulated industry ( medical device or pharmaceutical area). + Ability… more
    Envista Holdings Corporation (11/26/25)
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  • Director, Medical Events Group & NPR…

    Abbott (Alameda, CA)
    …8-10 years of experience in Quality Systems, Regulatory Affairs, or Quality Assurance within the medical device industry. * At least 5 years of ... Events Group (MEG) and No Product Return (NPR) will lead global medical device vigilance, post-market surveillance, and regulatory reporting for Abbott's… more
    Abbott (11/18/25)
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  • Quality Technician

    Aerotek (Caledonia, MI)
    …experience in a Quality Technician role. + Proficiency in quality assurance within a medical device environment. + Experience with FDA regulations, ... work in a dynamic environment where your expertise in quality assurance will be valued. Enjoy the...for this temporary role may include the following: * Medical , dental & vision * Critical Illness, Accident, and… more
    Aerotek (12/02/25)
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  • Mechanical Engineer

    Kelly Services (Janesville, WI)
    …technical leadership. Preferred Qualifications: Experience working within a nuclear quality assurance program or medical device QMS. Familiarity with ... Senior Mechanical Engineer - Regulated Industry Focus Location: Janesville, WI Industry: Medical Device and Nuclear Direct hire, permanent, benefits from day 1… more
    Kelly Services (11/24/25)
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  • Product Release Coordinator I

    Fujifilm (Santa Ana, CA)
    …science discipline is preferred. + A minimum of two (2) years of Quality Assurance in medical device manufacturer or equivalent. + Proficiency in current ... ie Detailed understanding of 21CFR211-cGMP, FDA QSR 820, ISO13485:2003, Canadian Medical Device Regulations and inspection and auditing guidelines. +… more
    Fujifilm (12/05/25)
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  • Quality Engineer

    Globus Medical, Inc. (Audubon, PA)
    …required (science or engineering preferred) + 3-5 years' experience in quality assurance ; experience in the medical device industry preferred + GMP ... maintaining compliance with US FDA and international medical device regulations and ISO 13485 quality system requirements. As a contributor to the quality more
    Globus Medical, Inc. (12/06/25)
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