Regulatory Affairs Intern

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profile Job Location:

Trumbull, CT - USA

profile Monthly Salary: Not Disclosed
Posted on: Yesterday
Vacancies: 1 Vacancy

Job Summary

Description

The Summer Intern program provides college students with the opportunity to participate in meaningful projects that contribute to the overall business unit addition to the assigned projects Interns are given the opportunity to participate in activities that encourage networking with peers managers and employees.

The Regulatory Affairs Intern will support the preparation organization and maintenance of regulatory documentation needed for medical device submissions and compliance activities. This role helps ensure products meet FDA and international regulatory requirements through handson involvement with daily RA tasks.



Responsibilities

Essential Functions & Accountabilities:

  • Support data integrity projects for new Regulatory Information Management (RIM) and Product Lifecycle Management systems implementation
  • Handles data entry data cleaning and any RA hold investigations
  • Support collaboration project to improve regulatory data management


Qualifications

Qualifications Knowledge Skills and Abilities:

  • Strong attention to detail and ability to manage multiple tasks.
  • Basic understanding of FDA or global medical device regulations (preferred not required).
  • Proficient in Microsoft CoPilot and Office (Word Excel PowerPoint).

Work Environment:

  • Professional office setting
  • Ability to work on-site 5 days a week at the Trumbull CT office.
  • This is a paid internship.
  • Prolonged sitting in front of a computer

Experience:

Any related course work preferred not required;

Internship experience is a plus.




Required Experience:

Intern

DescriptionThe Summer Intern program provides college students with the opportunity to participate in meaningful projects that contribute to the overall business unit addition to the assigned projects Interns are given the opportunity to participate in activities that encourage networking with peer...
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Key Skills

  • Proofreading
  • Adobe Acrobat
  • FDA Regulations
  • Manufacturing & Controls
  • Biotechnology
  • Clinical Trials
  • Research & Development
  • GLP
  • cGMP
  • Product Development
  • Chemistry
  • Writing Skills

About Company

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Live Brightly. Our daily and monthly soft contact lenses are designed with your health and comfort in mind. For every eye, every person, and every day.

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