• Clinical Evaluation, Project Manager - Clinical…

    Abbott (Maple Grove, MN)
    …devices clinical studies, and quality systems, MDD 93/42/EEC; MDR 2017/745; MEDDEV 2.7/1 Rev. 4; ISO 14971; ISO 14155; ISO 13485 + Effective written, verbal ... and presentation skills in the area of technical/clinical applications + Strong command of medical and surgical terminology + Project management and/or management of people experience + Demonstrated ability to identify and adapt to shifting priorities and… more
    Abbott (11/27/25)
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  • Multi-functional Manufacturing Supervisor - Level…

    Lockheed Martin (Fort Worth, TX)
    …for quality, cost, and schedule within your area, ensuring compliance with ISO 9001 and 14001 processes and standards\. * Training and Certification: Oversee ... a structured approach to improving manufacturing processes\. * Compliance\-Focused: Experienced with ISO 9001 and 14001 standards and audits, with the ability to… more
    Lockheed Martin (11/27/25)
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  • Supplier Quality Engineer

    Precipart (Farmingdale, NY)
    …supplier quality process in compliance with Precipart standards and other applicable regulations (eg, ISO 13485, AS9100 and ISO 9001). + Qualify new suppliers in ... and implement appropriate corrective actions to resolve concerns in line with ISO /AS, company, and customer requirements. + Stay current with best practices, trends,… more
    Precipart (11/27/25)
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  • Director, Global Quality - HealthTech

    Celestica (Maple Grove, MN)
    …suppliers, and partners, and ensuring compliance with regulatory requirements (FDA, ISO , ASQ, RAC). The position is virtual, offering competitive compensation and ... Understanding of validation principles and testing procedures. * Knowledge of FDA, ISO , RAC, and CQA regulations and standards. * Willingness to travel… more
    Celestica (11/27/25)
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  • Health & Safety Manager

    Prysmian (Claremont, NC)
    …+ Collaborates with Environmental Manager to achieve and maintain certification to ISO 14001:2015 and ISO 45001:2018 Standards (Integrated Management System). + ... of US health and safety regulations (OSHA). + Knowledge and Experience with ISO Management Systems a plus. + Knowledge of worker's compensation regulations. +… more
    Prysmian (11/27/25)
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  • Quality Specialist Level 2 (Corporate)

    MTA (New York, NY)
    …quality activities at various field sites and project offices. Supports ISO 9001 registration and compliance efforts by coordinating and actively participating ... in ISO audits and assessments. Prepares comprehensive audit and assessment...principles, methodologies, and best practices, with an understanding of ISO 9001 standards . Excellent communication and interpersonal skills.… more
    MTA (11/26/25)
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  • Manufacturing Quality Compliance Specialist - 2nd…

    Amcor (Jackson, TN)
    …report them immediately. + Report daily findings. + Must follow and comply with all ISO 9001, ISO 15378 established requirements + Must follow and comply with ... **Job ID** _2025-37942_ **Position Type** _Regular Full-Time_ **Category** _Quality Assurance & ISO Management_ **Location : Address** _1005 LOWER BROWNSVILLE ROAD_ more
    Amcor (11/26/25)
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  • Sr Quality Engineer I

    Gilead Sciences, Inc. (Foster City, CA)
    …improvement. + Ensure changes to commercial products comply with FDA QSR/QMSR, ISO 13485, and other applicable standards. + Maintain compliance with global Risk ... Management processes in accordance with ISO 14971 and other applicable standards. + Collaborate with...and tools (eg, Hazard Analysis, FMEA). + Knowledge of ISO 14971 Risk Management processes. + ASQ certifications (Certified… more
    Gilead Sciences, Inc. (11/26/25)
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  • Sr. Mgr., Regulatory Affairs (RA) & Clinical…

    Evident Scientific (Needham, MA)
    …and communications. + Ensure ongoing compliance with 21 CFR Part 820, ISO 13485, and MDSAP requirements. + Support QMS implementation, internal/external audits, and ... clinical study design, and QMS implementation. + Familiarity with ISO 14155, GCP, FDA 21 CFR 820, ISO... ISO 14155, GCP, FDA 21 CFR 820, ISO 13485, EU MDR/IVDR. + Strong project leadership and… more
    Evident Scientific (11/26/25)
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  • Clinical Product Manager - Medical Device Safety…

    Oracle (Helena, MT)
    …regulatory, and product leadership teams to align development activities with ISO 14971, IEC 62366, and EU/US Clinical Evaluation standards. Key Responsibilities ... . Conduct and contribute to clinical risk analyses (per ISO 14971). . Collaborate on Failure Mode and Effects...within healthcare technology or medical devices. . Knowledge of ISO 14971, IEC 62366, EU MDR/IVDR, and FDA guidance… more
    Oracle (11/25/25)
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