• Medical Device Process

    VTI Life Sciences (Naples, FL)
    …companies in the Life Sciences industry. We are looking for a Process Validation Engineer/Consultant for our Naples, Florida area medical device client ... Validation Services to the Pharmaceutical, Biotechnology, Biologics and Medical Device industries. VTI offers professional development, training, competitive… more
    VTI Life Sciences (12/07/25)
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  • Principal Member of Technical Staff…

    Oracle (Tallahassee, FL)
    …long-term technology strategy. You will guide product teams in interpreting and applying medical device standards (including IEC 62304, IEC 82304, and FDA ... support the adoption of compliant SDLC processes and tooling. Deep understanding of medical device software regulations and standards along with a proven… more
    Oracle (11/25/25)
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  • Clinical Product Manager - Medical

    Oracle (Tallahassee, FL)
    …is standing up a specialized clinical product management team focused on medical device -aligned products. This team bridges clinical practice, product strategy, ... usability, and compliance across our next-generation EHR and AI-enabled medical device platforms. As a Clinical Product...(IEC 62366), ensuring requirements map to user needs and validation meets usability and human factors standards. . Lead… more
    Oracle (11/25/25)
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  • Clinical Product Manager - Medical

    Oracle (Tallahassee, FL)
    …is standing up a specialized clinical product management team focused on medical device -aligned products. This team bridges clinical practice, product strategy, ... usability, and compliance across our next-generation EHR and AI-enabled medical device platforms. As a Clinical Product...(IEC 62366), ensuring requirements map to user needs and validation meets usability and human factors standards. . Lead… more
    Oracle (11/25/25)
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  • Staff Software Quality Engineer, Post Market

    Stryker (Orlando, FL)
    …Market** to support our Medical 's Digital Health division and portfolio Software as a Medical Device (SaMD)/Software in a Medical Device (SiMD) and ... in conjunction with R&D and Quality. + Work on process improvement projects while applying software industry practices, compliance...visualization and monitoring. + Exposure to Software as a Medical Device (SaMD), Software in a … more
    Stryker (12/10/25)
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  • Manager, Microbiology

    Bausch + Lomb (Clearwater, FL)
    …industry best practices. This includes the development, manufacturing and release of medical device product. KEY ACTIVITIES / RESPONSIBILITIES **Micro lab ... operational excellence and innovation. + 10-15 years of microbiology experience in biopharmaceutical/ medical device industry of which minimum of 5 years is… more
    Bausch + Lomb (09/18/25)
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  • Staff Fluoropolymer Extrusion Engineer (Onsite)

    Cordis (Miami Lakes, FL)
    …candidate has hands-on experience with extrusion process development, optimization, and validation in a regulated medical device environment. **Key ... to join our team. This role will focus on polymer and fluoropolymer extrusion for critical medical device components and catheter shaft assemblies. The ideal… more
    Cordis (10/15/25)
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  • Controls Engineer

    Kelly Services (Jacksonville, FL)
    …regulations, ISO standards, and GMP requirements specific to medical device manufacturing. + **Documentation & Validation ** Generate and maintain ... optimize control systems for advanced automated manufacturing equipment in a regulated medical device environment. You will be instrumental in improving… more
    Kelly Services (10/29/25)
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  • Manager, R&D Engineering

    Cordis (Miami Lakes, FL)
    …coating equipment, and packaging equipment + Oversees equipment qualification, test method validation , process validation , design validation testing, ... focus on hiring and managing a team of development, process , and combination device engineers. This role...product design transfer and commercialization + PMA Experience + Medical device product development and operations experience… more
    Cordis (10/08/25)
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  • Regulatory Affairs Associate Director, IVD

    GRAIL (Tallahassee, FL)
    …regulatory, development, clinical affairs, quality, or program management within the IVD, medical device , or pharmaceutical industries. + Regulatory affairs and ... Demonstrated knowledge of US and international regulatory frameworks and processes for medical device development and approvals. + Effective collaborator in… more
    GRAIL (12/03/25)
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