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    Regulatory Affairs Analyst - Burlington, United States - INTELLECTT INC

    INTELLECTT INC
    INTELLECTT INC Burlington, United States

    6 hours ago

    Intellectt Inc background
    Description
    Hello Everyone,

    Greetings of the day.

    This is Vydehi from Intellectt Inc. We currently have an opening for a Regulatory Affairs Analyst with one of our medical device clients. If you or anyone you know is interested in this opportunity, please feel free to send your updated resume to or reach out to me directly at

    Role :
    Regulatory Affairs Analyst


    Location :
    Burlington, MA

    Duration : 8-12 Months

    100% Onsite role (Only Local Candidates are applicable)

    Skills Looking For

    Entry-level position, but some relevant experience or exposure to regulatory affairs is beneficial.

    The project involves post-market surveillance, focusing on qualitative data related to patient experiences with medical devices, specifically the Heartmate pump.

    It is a computer-based role, with no hands-on involvement with the product.
    Strong time management, organizational skills, and ability to manage priorities effectively.
    Basic knowledge of Microsoft Office software.
    Background in STEM fields preferred, particularly biomedical engineering.
    Basic proficiency in Microsoft Office software is required.

    Day-to-day Responsibilities: Analyzing qualitative data regarding patient experiences with medical devices; Making decisions based on FDA regulations and international regulations; Collaborating with healthcare professionals, engineers, and field coordinators; Managing conflicting priorities and effectively communicating with team members.

    Education And Level Of Experience

    Bachelor's degree is required, preferably in STEM fields such as biomedical engineering.
    Entry level role (0 to 2 years of experience).

    Fresh graduate:
    Academic Achievements, Internships or Volunteer Work, Extra curricular activities during course work

    Overqualification Criteria


    Candidates with higher education levels (e.g., PhD or Masters) or extensive experience in the regulatory field may be considered overqualified for the entry-level nature of the role.

    Top 3 Skills

    Strong time management and organizational skills.
    Ability to manage priorities effectively in a fast-paced environment.
    Basic proficiency in Microsoft Office software.

    Interview Process

    Initial phone screening lasting 20-30 minutes followed by In-person interview.

    #J-18808-Ljbffr


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