Role Overview & Specifications
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 Jr
Location: Lake Forest, ILDuration: 08 Months
Description
Experience: 1+ years
experience in a medical device or similarly regulated industry
Skills: Ability to schedule and organize multiple projects
Education: BS Engineering or Scientific
Duties: 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.
About Intellectt Inc
Intellectt Inc is an actively verified employer hiring talent across technology, engineering, and operations.
- Headquarters: United States / United Kingdom
- Company Size: 1,000+ employees
- Trust Rating: 95 / 100 (Official Registry Audited)
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