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Intern, Qa Compliance Jobs

Company

Charles River Laboratories

Address , Rockville, 20850, Md
Employment type INTERN
Salary $20 an hour
Expires 2023-07-17
Posted at 1 year ago
Job Description

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

Job Summary


The QA Compliance, Intern is responsible to format, scan and upload all controlled GMP documentation in compliance with internal procedures and policies, as well as regulatory requirements into the Electronic Document Management System (EDMS).
Key Responsibilities and Duties:
  • Update document templates, project tracking logs, and databases through standard electronic formats.
  • Format controlled document templates.
  • Scan documents.
  • Help identify continuous improvement in document control processes.
  • Additional duties as assigned.
  • Create placeholders in the EDMS.

Job Qualifications



  • High School degree, preferred.
  • Strong organizational skills; able to prioritize and manage through complex processes/projects
  • Meticulous attention to detail
  • Good oral and written communication skills

The pay range for this position is $20.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

About Biologics Testing Solutions
With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.