For 75years, 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 role shall report to the Biosafety and Cell Based Assay Supervisor and the main duties and responsibilities shall be to assist the Department Manager in the following: - Execution of routine cell:based potency assays. - Support technical transfer, qualification and validation of new cell:based assays. - Maintenance and propagation of antibiotic free cell cultures. - Evaluation of mammalian cells / Generation and maintenance of mammalian cell banks. Core duties shall include: - Maintenance and propagation of antibiotic free cell cultures. - Competent in microscopic evaluation of mammalian cells (e.g. cell morphology, count and viability) - Receipt and processing of test samples in LIMS. - Support update current standard operating procedures. - Assist in laboratory investigations where necessary. - Support generation of GMP compliant SOPs, Protocols and reports - Generate risk assessments for laboratory and test items as required. - Maintain Laboratory Data Integrity and compliance. Job Qualifications The following are minimum requirements related to the In Vitro Analyst position. - BSc in a relevant science discipline (e.g. Biology, Biochemistry, etc.) - A minimum of 1 years relevant experience in Scientific Research preferably within a GMP regulated environment (EMEA/FDA) within the Pharmaceutical, Medical Device, CRO Industry is highly desirable. - Experience of aseptic cell culture techniques desirable. - Experience in in:vitro bioassays highly desirable. - Basic understanding off regulatory guidelines desirable. - Ability to problem solve and work on own initiative. 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 characterzation, 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 coordi