• Senior Project Engineer - Mechanical

    Globus Medical, Inc. (Methuen, MA)
    …Experience with drafting prints using GD&T and tolerance analysis + Experience in Medical Device field **Physical Demands** **:** The physical demands listed ... At Globus Medical , we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team… more
    Globus Medical, Inc. (08/16/25)
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  • Sales Representative - Specialty Medical

    Cardinal Health (Boston, MA)
    …including medical /surgical, copiers, payroll solutions, information) preferred + Medical Device industry experience preferred + Excellent phone, written, ... businesses. We offer industry expertise and an expanding portfolio of safe, effective medical products that improve quality , manage costs and reduce complexity.… more
    Cardinal Health (06/28/25)
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  • Trauma Specialist (Boston Metro Area)

    Globus Medical, Inc. (MA)
    …with disabilities to perform these_ essential _functions._ **Qualifications** **:** + 2+ years medical device sales or surgical related products experience and a ... At Globus Medical , we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team… more
    Globus Medical, Inc. (07/05/25)
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  • Medical Director, Gastrointestinal…

    Takeda Pharmaceuticals (Boston, MA)
    …issues with other functional areas such as Clinical Development, Regulatory Affairs, Quality Assurance, Medical Affairs, Marketing, Manufacturing, and Legal. + ... the Company-wide patient safety expert for assigned pharmaceutical / biological / drug- device combined products, accountable for the safety strategy and major safety… more
    Takeda Pharmaceuticals (09/04/25)
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  • Senior Software Developer (Android)

    ConvaTec (Lexington, MA)
    …as a Medical Device ) and SiMD (Software in a Medical Device ) mobile apps while ensuring high quality of the design and code, robustness of our ... Pioneering trusted medical solutions to improve the lives we touch:...performance, security, and scalability. + Design and develop high quality native Android applications using Kotlin and Java. +… more
    ConvaTec (08/16/25)
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  • Principal Field Clinical Engineer- North East

    Medtronic (Boston, MA)
    …**Nice to Have (Preferred Qualifications):** + Experience at Medtronic or within the medical device industry + Experience in the management of clinical devices. ... drive healthcare forward and remain a global leader in medical technology and solutions. To learn more about Inclusion...for all ablation procedures at study sites for investigational device studies to guide the physician on the requirements… more
    Medtronic (08/22/25)
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  • Senior Embedded Software Engineer - Verification…

    Capgemini (Burlington, MA)
    …ideal candidate will drive verification strategies, manage a team of engineers, and ensure compliance with medical device regulations. **Your Role** . Lead ... . Compliance & Standards: Ensure all verification activities align with relevant medical device regulations such as ISO 13485, IEC 62304, and FDA guidelines.… more
    Capgemini (07/31/25)
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  • Scientist I, Pharmaceutical Analysts

    Cardinal Health (Mansfield, MA)
    …Services Center perform laboratory testing to characterize the chemistries of our medical device products and stability testing for pharmaceutical products of ... protocols utilizing specialized instrumentation and analytical techniques to characterize medical devices, materials, and processing aids for chemical properties of… more
    Cardinal Health (09/03/25)
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  • Director, Design Assurance

    Hologic (Marlborough, MA)
    …States Are you a visionary leader with a passion for ensuring the highest standards of quality in medical device design and development? We are seeking a ... FDA Quality System Regulations, especially Design Control requirements, ISO 13485, and Medical Device Directive. + Familiarity with ISO 14970, IEC 60601, IEC… more
    Hologic (08/20/25)
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  • Director, Clinical Operations

    Bausch + Lomb (Boston, MA)
    …R&D/Project Management, Clinical/ Medical Affairs, Biometrics, Regulatory Affairs, Quality Assurance, Pharmacovigilance/GPSS and Drug/ Device Safety, and ... provide input on study-related documents and issues (DMP, SAP, drug/ device supplies, CSR, etc.). + Provides clinical operations input...ICH, GCP and B&L SOPs. + Responsible for the quality of all study-related documentation (eg, Trial Master File,… more
    Bausch + Lomb (09/06/25)
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