• Lead Clinical Laboratory Scientist

    Veterans Affairs, Veterans Health Administration (Houston, TX)
    …quality control(s) and quality assurance(s), following Food and Drug Administration ( FDA ) current Good Manufacturing Practices. Maintaining and ensuring that Quality ... of tests and evaluation of results, in accordance with AABB, CAP and FDA guidelines. Maintaining and monitoring conformity of Blood Bank SOPs. Ensures SOPs exist… more
    Veterans Affairs, Veterans Health Administration (01/04/26)
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  • Regulatory Affairs & Compliance Lead

    Carrier (Beverly, MA)
    …+ Interpret and monitor global regulatory requirements (eg, CE/MDR, FDA , ISO standards, environmental/transport regulations, wireless communications, data security). ... Certification (RAC) or equivalent professional certification + Regulatory Knowledge on US: FDA , FCC; EU: MDR, Radio Equipment Directive, Low Voltage, EMC; Canada,… more
    Carrier (01/04/26)
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  • Adaptive Optics Postdoctoral Fellow

    University of Maryland, Baltimore (Baltimore, MD)
    …for Devices and Radiological Health. The candidate will perform research with the FDA multimodal adaptive optics (mAO) imagers with a focus on retinal blood flow ... and assess imaging quality and performance of AO-enhanced ophthalmic devices. The well-equipped FDA labs contain several different AO and OCT imagers and are an… more
    University of Maryland, Baltimore (01/04/26)
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  • Patient Service Tech - Cmv

    Owens & Minor (Peoria, AZ)
    …preventive maintenance on vehicles is performed on a timely basis according to DOT, FDA and Joint Commission. + Responds to emergency delivery calls as needed and on ... Training Program. + Must meet job-related requirements to comply with DOT, FDA and Joint Commissions regulations. **SKILLS, KNOWLEDGE AND ABILITIES** + Business… more
    Owens & Minor (01/03/26)
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  • Assembler

    Aerotek (Medina, NY)
    …opportunities in a high-demand industry + **Clean, Climate-Controlled Facility:** FDA -regulated environment focused on safety and quality + **Comprehensive ... repairs. + Complete documentation for quality compliance. + Follow strict safety and FDA cGMP standards. **✅ What We're Looking For** + High school diploma or… more
    Aerotek (01/03/26)
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  • Supervisor, Shipping

    Fujifilm (Bothell, WA)
    …a strong sense of safety and of enforcing safe work practices. Ensure that FDA , ISO, OSHA and DOT standards for warehousing, distribution and employee safety are ... Experience in developing and implementing warehouse policies and procedures in an FDA or ISO quality system. **Skills/Abilities:** + Excellent customer focus and… more
    Fujifilm (01/03/26)
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  • Utilities Mechanic

    Bristol Myers Squibb (Devens, MA)
    …complies with company policies, EHS safety procedures, and regulatory requirements ( FDA , OSHA, EPA). + Collaborates with multidisciplinary teams to support facility ... documents, schematics, and regulatory guidelines. + Familiarity with GMP, FDA , and other regulatory requirements for environmental controls in manufacturing.… more
    Bristol Myers Squibb (01/03/26)
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  • Quality Assurance Manager

    GE HealthCare (Cleveland, OH)
    …Control activities to ensure that processes and outputs adhere to applicable FDA , EU regulations, ISO 13485:2016, and other governing regulations applicable to MIM ... Quality Management System requirements and regulatory requirements, including but not limited to FDA CFR 21 820, ISO 13485, and MDSAP. + Legal authorization to work… more
    GE HealthCare (01/03/26)
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  • Production Department Manager - Nutrition…

    Abbott (Casa Grande, AZ)
    …Ensure adherence to company quality systems and global regulatory standards, including FDA 21 CFR and international requirements for Infant Formula. Champion product ... environment. + Experience utilizing project planning and execution tools. + Knowledge of FDA - 21 CFR and other regulatory requirements for Infant Formula In… more
    Abbott (01/03/26)
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  • Sr QA Engineer - Design Control

    Insight Global (South San Francisco, CA)
    …activities across the IVD product lifecycle, ensuring compliance with ISO 13485, IVDR, FDA QSR, ISO 14971 and other global regulatory requirements. This role will ... QA lead on cross-functional product development teams, ensuring design control requirements ( FDA 21 CFR 820.30, ISO 13485, IVDR) are incorporated from planning… more
    Insight Global (01/03/26)
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