For more information please call:
1.877.CRIVER.1 (1.877.274.8371)askcharlesriver@crl.com
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Jul 06–Jul 10
Please stop by the Charles River booth to learn how our endotoxin and microbial detection products and services can help accelerate your research and drug development efforts through the integration of the Endosafe®-PTS™ in your lab process.
Aug 18–Aug 21
With the extensive application of LAL testing throughout the pharmaceutical and medical device industries, as well as biotechnology, dialysis and research, the need to advance skill levels and understanding is paramount. Charles River LAL Workshops have gained a reputation for providing LAL professionals with unrivaled technical and regulatory information, coupled with practical training. Our carefully developed program is strengthened by the participation of leading experts experienced in the LAL and pharmaceutical industry.
Charles River is looking for a Quality Assurance Inspector. The QA Inspector will be responsible for reporting study-specific audits in both process procedures and report texts. The QA Inspector will know Good Laboratory Practice regulation guidelines and Standard Operating Procedures as they apply to regulated research. The QA Inspector will also advise management of QA trends and assist in facility audits, system analyses, and training.
Responsibilities include conducting in-process inspections of study phases and analytical methods, audits of study data and final reports, and audits of internal facilities. Other responsibilities include establishing and maintaining quality assurance files and records and assisting with training requirements.
This position is responsible for managing the company’s business as it relates to Molecular Biology Services. Essential duties include ensuring on-time delivery of all client projects involving Bacterial Cell Line Characterization, DNA Hybridization Testing, Reverse Transcriptase Testing, Isoenzyme Analysis, and PCR assays; determining and implementing techniques to improve productivity, increase efficiencies, cut costs, and maintain state-of-the-art practices; refining and developing assays as needed to meet current industry standards; and assisting in the development of short- and long-range operating objectives, organizational structure, and staffing requirements.
The Principal Investigator I is responsible for advising sponsor organizations in the practical aspects of protocol; understanding study background, objectives, design, and criteria and having a full understanding of the investigational drug; overseeing clinical conduct of all studies; supervising the daily assessment of participants’ well-being; participating in and managing all phases of adverse events and related reporting; and participating in the writing and development of the final clinical summary.
Charles River Laboratories, Inc.