• Sr. Quality Engineer/C&Q

    Mentor Technical Group (Caguas, PR)
    …of (7) seven years' experience in manufacturing, quality control, quality assurance , or regulatory compliance, preferably in the medical device or ... the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas,… more
    Mentor Technical Group (11/01/25)
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  • Technical Quality Specialist

    Actalent (Kenosha, WI)
    …with calipers, micrometers, and blueprint reading. + Strong experience in quality assurance and control, particularly in the medical device sector. ... The Technical Quality Specialist is a pivotal role that intersects quality assurance , quality control, engineering, and manufacturing operations. This… more
    Actalent (12/06/25)
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  • Sr. Quality Systems Engineer

    Terumo Neuro (Aliso Viejo, CA)
    …(5) years of quality assurance /compliance related experience in the medical device industry. 3. Must be able to handle multiple projects concurrently, ... **13069BR** **Title:** Sr. Quality Systems Engineer **Job Description:** This is a...by collaborating with various functions (eg, R&D, Production, Field Assurance , etc.). + Facilitates CAPA Review Board meetings, prepares… more
    Terumo Neuro (10/16/25)
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  • Identity / Risk Management Field Operations…

    Huntington Ingalls Industries (Fort Meade, MD)
    …challenges. Leads small-scale projects, working groups, and operational initiatives. Quality & Compliance: Ensures high standards in documentation, reporting, and ... Expert Consultation: Expert understanding of 802.11 systems, Personal Electronic Device signature(s)/hardening, VPN/VPS architecture, and use of electronics in… more
    Huntington Ingalls Industries (12/04/25)
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  • Risk Control Design Quality Engineer

    Actalent (Irvine, CA)
    …experience in Design Quality Assurance and risk management within the medical device industry. + Certified Quality Engineer (CQE) or Risk Management ... preferred. + Experience with Class II or Class III medical devices. + Familiarity with electronic quality ...III medical devices. + Familiarity with electronic quality management systems (eQMS) and document control platforms. +… more
    Actalent (12/03/25)
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  • PMS Complaint Handling Specialist

    Philips (Cambridge, MA)
    …+ 0-2+ years of experience with Bachelor's in areas such as Complaint Handling Operations, Medical Device , Quality Assurance , Quality Control, ... Degree. Prefer 2+ years experience in Post-Market Surveillance, Vigilance Reporting in Medical Device . + Expertise in international regulations, including EU MDR… more
    Philips (12/04/25)
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  • Pharmaceutical Manufacturing Investigator

    Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
    …Pharmaceutical Sciences, or equivalent Experience: Minimum three years in Quality Assurance in the pharmaceutical, biopharmaceutical, or medical device ... of the Head of Operations and the Head of Quality Systems, the Deviation Investigator will play a pivotal...the site and abroad. They will routinely report on quality system and business process performance, proactively identifying, providing… more
    Glenmark Pharmaceuticals Inc., USA (11/26/25)
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  • Medical Devices Software Quality

    US Tech Solutions (San Bruno, CA)
    …solutions for a person based on a comprehensive view of the evidence. **Responsibilities:** ** Quality Assurance Champion:** 1. Act as a champion of Quality ... ISO 13485, and integration of best practices from the medical device industry. **Documentation and Support:** 1....including Google Suite. 2. Experience with diverse tools for quality assurance and engineering tasks, showing adaptability… more
    US Tech Solutions (10/17/25)
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  • Director - Software Process Excellence

    BD (Becton, Dickinson and Company) (San Diego, CA)
    …or RAC certification preferred). + 10+ years of progressive experience in Quality Assurance and Regulatory Affairs within the medical device or SaMD ... cross-functional teams (Engineering, Product Management, Product Security, Legal, Regulatory, Quality Assurance ) to embed quality ...(Software as a Medical Device ) industry. + Demonstrated success with FDA 510(k) and/or… more
    BD (Becton, Dickinson and Company) (10/11/25)
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  • NPD Quality Engineer II

    Terumo Medical Corporation (Elkton, MD)
    …mathematics, and statistics skills + Demonstrated working knowledge of key medical device related standards including 21 CFR 820 ( Quality Systems Medical ... Req ID: 5357 Location: Elkton, MD, US Company: Terumo Medical Corporation Department: TIS Design Assurance / Quality...scientific environment + Minimum of 2 years of experience in a regulated industry ( medical device industry… more
    Terumo Medical Corporation (12/09/25)
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