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 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.
ResponsibilitiesEssential 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
QualificationsQualifications 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...
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 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.
ResponsibilitiesEssential 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
QualificationsQualifications 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
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