• Principal Technical Program Manager…

    Oracle (Frankfort, KY)
    **Job Description** Oracle Health Data Intelligence (HDI) is hiring a Principal Technical Program Manager - Operations to lead key strategic and operational ... leadership, presenting data-driven recommendations and guiding cross-functional alignment. + ** Technical Documentation :** Help lead the efforts across both… more
    Oracle (12/20/25)
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  • Principal Member of Technical Staff…

    Oracle (Frankfort, KY)
    …development lifecycle, enabling teams to maintain compliance through automated traceability and documentation . + Support audits, technical documentation , and ... **Job Description** As a Principal Member of Technical Staff, you...and relevant FDA guidance. + Proven ability to apply regulatory requirements to software design, documentation , and… more
    Oracle (11/25/25)
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  • Senior/ Principal Technical Program…

    Oracle (Frankfort, KY)
    …focus on excellence. **The Role** We are looking for an experienced Technical Program Manager who is proactive, results-oriented, and demonstrates strong ownership ... Program Management and Engineering to improve SLAs and mitigate risk, ensure regulatory compliance, and advance operational integrity. Serve as a trusted partner for… more
    Oracle (12/23/25)
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  • Principal Transformation Technical

    Oracle (Frankfort, KY)
    …stakeholders, manage high-stakes vendor relationships, and navigate the complexities of regulatory compliance. Your ability to anticipate and mitigate risks to ... with internal teams to make sure we deliver the proper design and process documentation to the Colo, execute on our ISP circuit contracts, and update all internal… more
    Oracle (01/03/26)
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  • Senior Principal Applied Scientist

    Oracle (Frankfort, KY)
    …years of experience in AI/ML solution development, with 5+ years in senior or principal technical roles. + Proven track record leading large-scale, production AI ... discussions, helping shape the future of responsible healthcare AI. + Publish technical insights, speak at conferences, and mentor Principal -level engineers and… more
    Oracle (11/25/25)
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  • Principal TPM, SaMD (Remote)

    Oracle (Frankfort, KY)
    …surveillance processes are embedded into SDLC activities. + Translate regulatory requirements into clear engineering controls, documentation workflows, ... engineering programs in regulated environments. + Demonstrated ability to translate regulatory requirements into technical workflows, SDLC practices, and… more
    Oracle (12/22/25)
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  • Principal SaMD Quality & Compliance Manager…

    Oracle (Frankfort, KY)
    … Scientists, Engineering, Product, and Security to ensure submissions and technical documentation meet approval standards. **Design Controls & Risk** ... Manager** to lead and mature our quality systems and regulatory readiness for AI-enabled Software as a Medical Device...and digital health solutions. This role sits within HDI's ** Regulatory & Medical Device organization.** You will serve as… more
    Oracle (01/10/26)
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  • Principal Supply Chain Data Scientist

    Genentech (Louisville, KY)
    …people feel valued, included and able to thrive. **The Opportunity** As the Principal Supply Chain Data Scientist, you will lead advanced analytical initiatives to ... process optimization, and strategic supply chain insights. This position combines technical expertise, leadership, and collaboration to impact the broader supply… more
    Genentech (12/03/25)
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  • Principal Software Developer - DevOps…

    Oracle (Frankfort, KY)
    …with regulatory and organizational requirements. + Write and maintain technical documentation , including software design and standard operating procedures. + ... **Job Description** Join our innovative automation team as a Principal Software Developer, focused on designing, developing, and maintaining software-driven… more
    Oracle (12/20/25)
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  • Principal Medical Writer / Senior Medical…

    Parexel (Frankfort, KY)
    …to prepare, develop, and finalize clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, investigator ... model informed consents, interim and final clinical study reports, common technical document (CTD) clinical overviews and summaries, safety update/aggregate reports,… more
    Parexel (12/13/25)
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