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    Regulatory Specialist II - Santa Clara, United States - DivIHN Integration

    DivIHN Integration
    DivIHN Integration Santa Clara, United States

    11 hours ago

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    Description

    DivIHN (pronounced divine) is a CMMI ML3-certified Technology and Talent solutions firm. Driven by a unique Purpose, Culture, and Value Delivery Model, we enable meaningful connections between talented professionals and forward-thinking organizations. Since our formation in 2002, organizations across commercial and public sectors have been trusting us to help build their teams with exceptional temporary and permanent talent.

    Visit us at

    to learn more and view our open positions.

    Please apply or call one of us to learn more

    For further inquiries regarding the following opportunity, please contact one of our Talent Specialists
    Rashi at
    Divya at

    Title: Regulatory Specialist II
    Location: Santa Clara, CA
    Duration: 6 Months

    Description:

    Exempt/Non Exempt:
    Non Exempt Years

    Duties:
    Responsible for implementing and maintaining the effectiveness of the quality system.
    Supports manufacturing/operations day to day activities for change control.
    Provides consultation/advice to regulatory specialist for change control and product development.
    Provides regulatory direction/interpretation on team activities.
    Interprets and applies regulatory understanding to support of products and teams.
    Prepares U.S. regulatory submissions and/or registration documents for international affiliates and government agencies worldwide.
    Handles regulatory activities involved in documentation,labeling,field support.
    Applies regulatory and technical knowledge to a wide variety of complex work assignments.
    Maintains and ensures compliance to the appropriate quality system for the specific medical device(s) designed or manufactured that the individual supports.
    Ensures compliance to and is able to demonstrate knowledge of site and division level policies and procedures.

    Experience:
    2-5 years regulatory experience and/or 2 years relevant industrial experience typically with a quality, product-development/support, or scientific affairs function.
    Seeking candidate with experience with international (outside of EU and US) product registrations; experience working with medical device operations on control of product release; experience working with electronic change management/document control systems.

    Skills:
    Knowledge of regulations and standards affecting IVDs and/or biologics.

    Education:
    BS preferred in a technical discipline like biology, chemistry, microbiology, immunology, medical technology, etc.

    About us:

    DivIHN, the 'IT Asset Performance Services' organization, provides Professional Consulting, Custom Projects, and Professional Resource Augmentation services to clients in the Mid-West and beyond. The strategic characteristics of the organization are Standardization, Specialization, and Collaboration.

    DivIHN is an equal opportunity employer. DivIHN does not and shall not discriminate against any employee or qualified applicant on the basis of race, color, religion (creed), gender, gender expression, age, national origin (ancestry), disability, marital status, sexual orientation, or military status.

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