Regulatory Affairs Associate Jr
📋 Role Overview & Responsibilities
Hello Everyone,Greetings of the day.This is Vydehi from Intellectt Inc. We currently have an opening for a Regulatory Affairs Associate Jr 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 vydehi@intellectt.com or reach out to me directly at +1 732 355 7412.
Role: Regulatory Affairs Associate JrLocation: Lake Forest, ILDuration: 08 Months
Description:Experience: 1+ years experience in a medical device or similarly regulated industrySkills: Ability to schedule and organize multiple projectsEducation: BS Engineering or ScientificDuties: Manager regulatory submissions to ensure timely regulatory approval of medical devices. Monitor changing regulations in geographies and translate/communicate these requirements to project development and/or continuous improvement project teams. Ensure all client product and procedures comply with applicable regulatory agency requirements and guidelines.
Top 5 skills/requirements - Strong analytical and problem-solving skills. Demonstrated competency and working knowledge of Excel, Word, PowerPoint, SharePoint, and Teams. Communicate effectively verbally and in writing. Communicate with diverse audiences and personnel. Write and edit technical documents. Ability to work with people from various disciplines and cultures. Strong attention to detail. Good organizational / project management skills to manage and track a wide range of tasks; ability to develop realistic action plans as well as prioritizing work activities.
Interview:Confirm interview preferences (phone, onsite, video): Initial interview via phone/video, 30 min. Then, select 2 or 3 candidates for an onsite interview.
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This position is located in Lake Forest, IL with potential relocation and sponsorship assistance depending on candidate qualifications.
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