This job posting may have expired!
Use our `search` to find similar offers.
Similar jobs

QC RMG Summer 2023 Intern

Charles River Laboratories International Inc (CRL)

Memphis, TN, US, 38118

Job Summary

The Intern is responsible for successfully completing the internship program course leading up to the potential involvement of various technology related activities associated with the start-up and GMP production of a number of novel cellular products including compliance with regulatory agencies and associated guidelines. Must be able to meet physical requirements established in this job description.    

  • Obtain and maintain qualifications necessary for the performance of aseptic activities.
  • Consistently practice appropriate clean room behaviors.
  • Obtain detailed knowledge of 21 CFR Part 11 compliance as it pertains to implementation of regulated systems.
  • Display an ability to create necessary system and regulatory documentation.
  • Strong communication skills for cross departmental preparation of new equipment set up.
  • Display an ability to troubleshoot issues.
  • Exhibit a sense of urgency in completion of necessary documentation
  • Perform other duties as assigned.

Job Qualifications

  • Currently enrolled in a Bachelor or Associate’s program focused in Information Technology, Systems Engineering, or related curriculum. Minimum of 3.0 GPA preferred. 
  • Must be able to work in a clean room environment.
  • Must be detailed oriented and have excellent organizational skills.
  • Must possess effective written and oral communication skills.
  • Must display a high degree of professionalism and confidentiality. 

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.

About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. 

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.

Equal Employment OpportunityCharles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin, veteran or disability status.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

Job posted: 2023-03-27

Подписаться