• Quality Engineer III

    Actalent (Worcester, MA)
    …Engineering, Life Sciences, or a related field. + Experience in pharmaceutical, medical device , or biologics manufacturing environments. + Strong understanding ... products, and biologics. This role plays a key part in driving strategic quality initiatives and ensuring compliance with regulatory and internal standards. Key… more
    Actalent (08/08/25)
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  • Director - Packaging Technology

    Sanofi Group (Cambridge, MA)
    …and bring hope to patients and their families. The strategic vision of Sanofi's Global Medical Device and Packaging organization is to lead the industry in ... market auto-injectors, pens, safety syringes, as well as connected medical device technologies, and we are gearing...equipment, printing, and vision control systems. + Knowledge of device and packaging regulations, quality systems, design… more
    Sanofi Group (08/08/25)
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  • Senior Quality Engineer I - Design…

    Integra LifeSciences (Braintree, MA)
    …(Biomedical or Mechanical) or related discipline with 5+ years of experience in Quality Assurance role for medical device or pharmaceutical manufacturing, ... activities. The role works closely with Product Development, Project Management, Regulatory , Marketing and Medical Affairs. **ESSENTIAL DUTIES AND… more
    Integra LifeSciences (08/08/25)
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  • Quality Control Manager

    Kelly Services (Norwood, MA)
    …+ **Hands-on experience with:** + **Root cause analysis and CAPA processes** + ** Regulatory compliance (eg, medical device reporting, product risk ... ** Quality Control Manager** _Location: Norwood, MA (Relocating to...**ISO 9001 and ISO 13485** standards and all applicable legal/ regulatory requirements. + Coordinate **internal and external audits** ,… more
    Kelly Services (08/01/25)
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  • Senior Engineer, Design Transfer Specialist

    Amgen (Cambridge, MA)
    …sites. This role requires a deep understanding of medical device design, manufacturing processes, and regulatory requirements. Key Responsibilities: + ... years of progressive experience as an engineer or scientist in relevant fields ( medical device development, manufacturing, etc.) + Proven track record of… more
    Amgen (08/08/25)
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  • Principal Electrical Supplier Quality

    Hologic (Marlborough, MA)
    …Supplier Quality Engineering roles. + 5+ years of experience in medical device manufacturing or related industries. + Hands-on experience with manufacturing ... team! In this role, you'll execute activities to ensure compliance with regulatory standards and Quality Management System requirements, conduct technical… more
    Hologic (07/21/25)
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  • Quality Engineer II - Design & Reliability…

    Integra LifeSciences (Braintree, MA)
    …(Biomedical or Mechanical) or related discipline, with 3+ years of experience in Quality Assurance role for medical device or pharmaceutical manufacturing, ... testing activities. The role works with Product Development, Project Management, Regulatory , Marketing and Medical Affairs. **ESSENTIAL DUTIES AND… more
    Integra LifeSciences (06/07/25)
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  • Quality Engineer II (Manufacturing)

    Teleflex (Chelmsford, MA)
    Quality Engineer II (Manufacturing) **Date:** Jul 15, 2025 **Location:** Chelmsford, MA, US **Company:** Teleflex **Expected Travel** : Up to 10% **Requisition ID** ... :12403 **About Teleflex Incorporated** As a global provider of medical technologies, Teleflex is driven by our purpose to...driven by our purpose to improve the health and quality of people's lives. Through our vision to become… more
    Teleflex (07/16/25)
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  • Manager, Quality

    ThermoFisher Scientific (Ward Hill, MA)
    …Proven ability in a Quality Assurance position within the Chemical, Medical Device or Pharmaceutical Industries supporting Regulated Products. + Minimum 2-3 ... **Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** Quality Manager US Full-Time Internal/External When you join Thermo… more
    ThermoFisher Scientific (08/08/25)
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  • Supplier Quality Engineer II

    Medtronic (Billerica, MA)
    …metal precision processing, and adhesives for the Catheter/Disposable SQE position. + Medical device manufacturing industry experience, preferably ISO 13485. + ... skills and ability to lead cross-functional teams. + In-depth knowledge of quality systems, standards, and regulatory requirements. + Excellent communication and… more
    Medtronic (08/02/25)
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