• Sr cGMP Specialist - QC Analytical Radiochemist

    Houston Methodist (Houston, TX)
    …customer service focus and application of positive language principles + Familiar with quality , compliance and FDA regulatory requirements for Good ... and devices. Additionally, this position will be responsible for all aspects of compliance associated with the quality operations including, but not limited to,… more
    Houston Methodist (07/30/25)
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  • Quality Manager- Medical Device…

    Ricoh Americas Corporation (Indianapolis, IN)
    …equipment requirements, and to acquire and maintain the equipment necessary to validate product quality . + Ensures compliance with FDA , HIPAA, and other ... quality of materials, products, systems, and processes in compliance with 21 CFR 820, ISO 13485, and other...compliance to specifications. + Drives tactical and strategic quality improvement plans, and all quality related… more
    Ricoh Americas Corporation (07/29/25)
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  • Quality Technician

    Trane Technologies (Noblesville, IN)
    …to reach outcomes that gain all parties' support and acceptance while maintaining quality standards and compliance to FDA /ISO guidelines. + Demonstrates ... what's possible for a sustainable world. **Trane** **Technologies** is currently seeking a ** Quality Technician** **.** As a Quality Technician, you will support… more
    Trane Technologies (07/08/25)
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  • Compliance Head, US FDA

    Sanofi Group (Framingham, MA)
    …Team + **Lead cGMP compliance projects** aligned with the company's Quality Operations strategy and US FDA regulations. + **Drive digital transformation ... **Job Title:** Compliance Head- US FDA **Location** :...**Core member of critical governance** + Sanofi's GMP GDP Quality Council to facilitate sharing of US FDA… more
    Sanofi Group (06/03/25)
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  • Manager, Quality Assurance & Regulatory

    Tecomet (Woburn, MA)
    …and improve quality systems/programs, reduce quality costs and maintain compliance within FDA and ISO regulations. This is accomplished by maintaining ... Correspondent. + Serve as person responsible for regulatory compliance (PRRC). + Assist and complete site FDA...procedures to ensure is in compliance with FDA 21 CFR, Part 820, Quality System… more
    Tecomet (07/31/25)
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  • Biomedical Equipment Technician IV (GA)

    BioBridge Global (Norcross, GA)
    …according to Standard Operating Procedures (SOPs) and policies. Must maintain familiarity of regulatory/ quality compliance , to include FDA , EU, ISO, GHM, ... _QualTex Laboratories is an FDA -registered and CLIA-certified organization that provides state-of-the-art, high...the company's laboratory equipment assets all while remaining in compliance with local, state and federal regulations. This position… more
    BioBridge Global (06/17/25)
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  • Head Of Quality

    Actalent (Lexington, MA)
    … Quality team. Required Skills: + Quality Assurance + Audit Management + FDA Compliance + CAPA Oversight + GMP/GxP Knowledge + CDMO Experience Top Skills: ... Description: Lead and oversee the Quality team, ensuring robust compliance with...Quality Assurance (QA), including audits, CAPA oversight, and FDA readiness, while maintaining and improving QA systems across… more
    Actalent (07/26/25)
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  • Validation Specialist II

    BioBridge Global (San Antonio, TX)
    …and/or verifications from start to finish. **Knowledge** Must maintain familiarity of regulatory/ quality compliance , to include FDA , EU, ISO, GHM, ... and able to develop effective relationships with internal partners such as enterprise Quality and Compliance Departments to ensure that validations go smoothly.… more
    BioBridge Global (06/09/25)
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  • Material Handling & Quality Assurance…

    ARTIDIS (Houston, TX)
    …of received goods + Execute all local Quality Management activities in compliance with FDA Requirements + Ensure compliance assurance and monitoring ... or diagnostics environment + Sound knowledge of ISO 13485:2016 and an understanding of FDA Quality System Regulation (21 CFR Part 820) + Hands-on experience in… more
    ARTIDIS (07/04/25)
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  • Validation Engineer I

    Teva Pharmaceuticals (West Chester, PA)
    …science or engineering PREFERRED QUALIFICATIONS: + Knowledge of validation and quality compliance (cGMP/ICH/ FDA /USP/EP policies/guidelines) + Validation ... lifecycle documentation, eg SOPs, Change Controls, CAPAs, Deviations, ensuring compliance with in-house specifications, standards and procedures, and implementing… more
    Teva Pharmaceuticals (07/26/25)
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