Charles River Laboratories

Familiarity with laser particle counters, viable air samplers, microscope, Endosafe Instrumentation, PCR, BacT/ALERT systems. 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.. 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.. Job Segment: Biology, Biotech, Microbiology, Pharmaceutical, Laboratory, Science

assurance associate

Sterility Assurance Associate IIReq ID #: 222136Location:Memphis, TN, US, 38118 Memphis, TN, US, 38118For 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 SummaryAs our Sterility Assurance Associate, you will develop to become a SME for sterility assurance joining a talented and diverse team playing a key role in ensuring that all products leaving Charles River Laboratories meet the standards required.ESSENTIAL DUTIES AND RESPONSIBILITIES:* Work closely with the operations group.* Partner with the QC Micro Lab to develop the clean utilities and environmental monitoring program for the site* Establish, in conjunction with the operations function, the sites gowning strategy and cleaning and sanitization program* Liaise with the global science and technology team to ensure best practices are in place concerning sterility assurance* Collaborate with cross-functional teams for the transfer of microbiological test methods to the site* Maintain site practices for contamination control etc. utilizing training and a purposeful presence on the operations floor* Influence operations area owners to ensure that quality issues are identified, and appropriate corrective actions are implemented to maintain compliance* Comply with the EHS&S policy and procedures and demonstrate EHS&S best practices in all work activities.* Adhere to and follows all procedures, policies, and guidelines ensuring compliance with cGMP and HPRA/FDA regulations and company policies, procedures, and guidelines* Perform other duties as assigned.Job Qualifications* Bachelor's degree in biology or relevant scientific discipline preferred* Minimum 1-3 years relevant laboratory experience or experience in a cGMP and/or FDA regulated industry* Demonstrated knowledge in Microbiology and aseptic techniques* Ability to work independently or as a team member* Detail-oriented with strong written and verbal communication skills* Ability to problem-solve and troubleshoot as necessary* Familiarity with laser particle counters, viable air samplers, microscope, Endosafe Instrumentation, PCR, BacT/ALERT systems* Demonstrated knowledge in decision based data trending and investigations for system/process improvements* Ability to work independently or as a team member* Detail-oriented with strong written and verbal communication skillsCompensation DataThe pay range for this position is $25.97 - $29.33 per hour. Please note that salaries vary within the range based on factors but not limited to experience, skills, education and location.About Biologics Testing SolutionsWith 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 RiverCharles 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.For more information, please visit www.criver.com.Nearest Major Market: MemphisJob Segment: Biology, Biotech, Microbiology, Pharmaceutical, Laboratory, Science

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