QC Analyst I Flow Cytometry 1:00pm - 9:30pm Monday thru Friday

　　Req ID #: 221025

　　Location:

　　Memphis, TN, US, 38118Memphis, TN, US, 38118

　　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

　　This shift is 1:00pm - 9:30pm Monday thru Friday

　　QC Analyst I performs flow cytometry for our Quality Control Analytical Department. The successful candidate will be responsible for performing routine quality control product and raw material release testing utilizing multi-color flow cytometry as well as various biochemistry, molecular biology, and general laboratory techniques according to GMP. Additionally, the analyst will assist QC Scientists with technology transfer of new client assays by Co-authoring SOPs or other required documentation.

　　The position requires the utmost attention to detail, very strong organizational skills, computer proficiency, and a basic understanding of laboratory instrumentation. In addition, effective communication skills and the ability to function in a fast-paced, highly technical environment with minimal supervision are essential for success.

　　Perform routine in-process and final release assessments of products using multicolor flow cytometry

　　Reviews test results of other QC analysts for accuracy and precision and maintains efficient workflow of all required testing documentation ensuring timely submission relative to product release dates

　　Enters assay results into the appropriate trending databases for periodic analysis

　　Assists the QC Team with maintaining proper overall operation of department (physical inventories, logs, documentation, filing, etc.)

　　Maintains familiarity with QC-relevant cGMP guidance’s (CFR, USP, EP, ICH, etc.)

　　Co-drafts new SOPs or other documentation, as required, in support of new procedures adopted by the QC Department, either internally or at client request

　　Assists with the implementation of quality improvement initiatives for QC laboratory operations

　　Participates in laboratory, OOS, CAPA or other investigations, as required

　　Maintains laboratory supplies, media and reagents inventory

　　Job Qualifications

　　Bachelors or higher degree in the biological sciences or related field preferred

　　High school diploma or equivalent required

　　At least 4 years relevant laboratory experience preferred

　　1-2 years of experience in cGMP/FDA regulated industry preferred

　　May consider less education and professional experience upon successful completion of Charles River’s internship program.

　　Ability to work independently and as part of a team

　　Demonstrated knowledge in “core” laboratory techniques (e.g. ELISA, cell culture/counting, PCR, etc.) and aseptic techniques required

　　Detail-oriented with strong written and verbal communication skills

　　Ability to problem-solve and troubleshoot as necessary

　　Previous experience running multi-color flow cytometry or familiarity with FACS Canto II flow cytometer or similar preferred but not required.

　　Compensation Data

　　The pay range for this position is $42,000K - $46,000K. 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.

　　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 Opportunity

　　Charles 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 [email protected] . 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.