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    Job · 17128541

    E Merge Tech Global Services logo

    Medical Device Regulatory Operations Associate

    E Merge Tech Global Services · Chennai · onsite · Posted 41d ago

    Undisclosed0–4 yrsfulltimeSourced fromNaukri

    About a minute. You'll make an account on the way through.

    About this role

    • Manage and coordinate medical device regulatory operations activities.
    • Develop and implement effective regulatory strategies to ensure compliance with industry standards.
    • Collaborate with cross-functional teams to resolve regulatory issues and improve processes.
    • Conduct thorough reviews of regulatory documents and submissions.
    • Provide training and guidance on regulatory requirements to internal stakeholders.
    • Stay up-to-date with changing regulatory requirements and industry trends.


    Disclaimer: This job posting & Location has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

    Sourced from naukri

    Skills

    clinical researchtechnology transferRegulatory AffairsEctdUSFDACAPAICHFormulation Developmentregulatory operationsRimProject ManagementQuality AssuranceQuality ControlResearchProduct DevelopmentResearch And Development

    About E Merge Tech Global Services

    E Merge Tech Global Services logo

    E Merge Tech Global Services

    Analytics & KPO

    11

    employees

    2007

    19 years old

    Chennai, Tamil Nadu

    India

    ₹3.3L PA avg

    Avg at E Merge Tech Global Services

    About

    E Merge Tech provides knowledge-intensive solutions across scientific and legal fields, helping clients tackle complex challenges with expert services.

    Industries

    Analytics & KPO

    Employee ratings

    10 reviews

    2.8/ 5

    Culture

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    2.9

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    Medical Device Regulatory Operations Associate · waiting for your command