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Trenton

    USA - Regulatory Affairs Associate - Trenton, United States - Saviance Technologies

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    Description
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    Onsite - Yes
    Regulatory Affairs Labeling Associate Level

    I is needed to support Client


    business to prepare and review regulatory labeling deliverables based on Reference Listed Drug labeling, FDA Guidance, regulation and Client internal practices.

    Support labeling review process with a Quality Assurance and data integrity mindset. Apply team concept to get things done and work collaboratively with everyone with transparency.

    Applying strategic thinking, pharmaceutical educational knowledge, and regulatory intelligence during preparation and review.

    Utilizing technical skills for learning new features and /or applications software which can support preparation and review activities.

    Some key traits, should have Pharmaceutical Experience, worked in control environment to follow process, quality focus. An effective communicator and can work independently and collaboratively with everyone, additionally, having Generic labeling experience is a plus.


    Education:
    Bachelor's or Associate s degree in a scientific or English discipline.


    Experience:
    Bachelor s degree plus a minimum of 1 -2 years in the pharmaceutical industry with 1 of those years working with labeling, conducting reviews or

    Associate s degree plus a minimum of 3-4 years pharmaceutical industry experience working with labeling, conducting reviews.
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