Bedford, MA, US
8 hours ago
Regulatory Affairs Intern
Welcome page Returning Candidate? Log back in! Regulatory Affairs Intern Job Locations US-MA-Bedford Job ID 2025-8302 Type Intern Shift 1st Category Quality Assurance/Regulatory Affairs Overview

Overview:

 

The purpose of the internship is to provide meaningful professional hands-on experience to students with leadership potential and proven academic performance.  Werfen hires students majoring in Engineering and Life Sciences fields into this internship program based on business need.  Ideal candidates will combine technical and business knowledge with analytical strength and creative problem-solving abilities. 

Responsibilities

Position Description

Create Change Orders to update regulatory documentation and Standard Operating Procedures as neededSupport the organization of regulatory files through Werfen’s electronic Regulatory Affairs DatabaseCompile documentation to support new regulatory filings to health authorities (including FDA 510(k) submissions and IVDR Technical Files in Europe)Perform regulatory administrative tasks as needed

Key Attributes 

Currently enrolled in a Bachelor’s or Graduate degree program Ability to handle multiple priorities, projects and assignments simultaneously.Strong analytical and interpersonal skills.Strong proficiency using Microsoft Office (Excel, Word, PowerPoint). Ensure and maintain compliance with the Company’s quality system requirements through training and adherence to policies, procedures and processes.Other duties as assigned. Qualifications Minimum Knowledge & Experience Required for the Position:Currently pursuing B.S. in Regulatory Affairs, Life Sciences, Engineering, Finance, Business, or Marketing with a minimum of 2 college semesters complete.Ability to multitask. Options Apply for this job onlineApplyShareRefer a friendRefer Sorry the Share function is not working properly at this moment. Please refresh the page and try again later. Share on your newsfeed Application FAQs

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