• Qms Specialist

    Actalent (Boston, MA)
    Job Title: QMS Specialist (25/hrs. per week) We are seeking a highly skilled QMS Specialist with experience in a GMP-regulated environment, ideally ... regulations for GMP compliance is essential. Responsibilities + Assess current QMS processes, identify areas for improvement, and implement effective solutions to… more
    Actalent (05/14/25)
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  • Cybersecurity & Application Specialist

    Carrier (Beverly, MA)
    …. **About This Role:** The Cybersecurity & Application Specialist operates independently, conducting multidisciplinary research and performing System ... to identify, prioritize, and address security-related issues. Additionally, the specialist provides assurance, both internally and externally, to demonstrate the… more
    Carrier (05/22/25)
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  • Medical Device Reporting Specialist

    Hologic (Marlborough, MA)
    Medical Device Reporting Specialist Marlborough, MA, United States We are seeking a detail-oriented and proactive Medical Device Reporting Specialist to join our ... ensuring compliance with applicable regulations and quality management systems ( QMS ) requirements, specifically related to the assessment, documentation, and… more
    Hologic (05/31/25)
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  • Senior Validation Specialist - Computer…

    Regeneron Pharmaceuticals (Cambridge, MA)
    We are seeking a highly skilled, self-motivated **Senior Validation Specialist - CSV** to ensure compliance of computerized systems with regulatory requirements in ... GAMP 5, and Annex 11. **As a Senior Validation Specialist , a typical day might include:** + Planning and...facility; GMP experience is required. Experience with ERP, LIMS, QMS and other GxP-regulated computerized systems and analytical instruments… more
    Regeneron Pharmaceuticals (05/10/25)
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  • Senior Regulatory Affairs Specialist - ACM

    Medtronic (Mansfield, MA)
    …world. **A Day in the Life** We are seeking a Senior Regulatory Affairs Specialist to join our team within Medtronic Acute Care and Monitoring (ACM). In this ... standards (eg, ISO 13485), and experience with Quality Management Systems ( QMS ) + Technical Writing + International medical device regulatory submission/approval… more
    Medtronic (05/29/25)
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