Charles River Laboratories
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Seeking a Project Manager 3 to oversee staff activities, coordinate client interactions, and manage facility maintenance. Requires a Bachelor of Science in Animal Science, 4-6 years of management experience, and AALAS certification. Hourly rate of $53 to $58 USD.
Coordinate study-related activities to ensure compliance with protocols and SOPs. Provide training, identify process improvements, and lead activities in compliance with GLPs and SOPs.
As a Materials Control Analyst, responsible for managing materials efficiently to support testing and meet client demands. Includes updating Supply Chain Database, documenting material movements, and contributing to raw material requests and purchase requisitions. Also involves analyzing inventory needs, maintaining accurate records, and identifying areas for improvement in material usage patterns. Must comply with SOPs and GDP, conduct cycle counts, and ensure materials meet specifications.
Responsible for managing complex Process Development and Good Manufacturing Practices (GMP) Manufacturing projects, providing mentorship to junior project management professionals, coordinating project communications, overseeing project start-up tasks, managing project timelines, collaborating with cross-functional teams, advising clients on project scope, and developing project management tools.
Responsible for coordinating maintenance and alteration of equipment, facilities, and buildings. Develop preventive maintenance schedules, evaluate equipment conditions, and support engineering projects. Manage contractors, update equipment records, and perform sizing calculations on equipment. Support sustainability efforts and reduce energy/water consumption.
Coordinate IACUC functions and the review process across multiple sites, ensuring compliance with regulations and policies related to animal research protocols.
The Qualification Coordinator is responsible for personnel qualifications in a Cell Therapy Manufacturing Facility in Memphis, Tennessee. Key responsibilities include scheduling, executing, and maintaining qualifications for personnel, maintaining qualification records, training personnel, and drafting Quality Management System documents.
Serve as a scientist in the Virology Department performing research duties including assay optimization, study development and management, interpretation of study data, and ensuring regulatory compliance. Supervise employees involved in research and development of testing procedures. Assist in protocol generation, lab coordination, statistical analysis, client study management, and personnel training.
Seeking a Scientist II specializing in Mass Spectrometry for the development and execution of testing and characterization of biotherapeutics. Responsibilities include implementing and qualifying mass spectrometry equipment, developing laboratory experiments, managing projects, and mentoring technical staff. Must have a Bachelor's degree in Chemistry/Biochemistry or related discipline with a minimum of 5 years of relevant experience.
The Client Manager (CM) role manages client relationships, facilitates communication between clients and CRL scientific teams, and collaborates with business development, scientific, and financial staff to ensure quality customer satisfaction is provided.
Responsible for financial performance analysis, variance analysis, client invoicing, and supporting business reviews. Utilizes SAP, AFO, and SAC applications for reporting. Requires a Bachelor's degree with 3-5+ years of experience in the Life Science industry.