With a location in Boothwyn, Charles River provides essential products and services to help pharmaceutical and biotechnology companies, government agencies, and leading academic institutions around the globe accelerate their research and drug development efforts.
Charles River’s dedicated employees are focused on providing clients with exactly what they need to improve and expedite the discovery, early-stage development, and safe manufacture of new therapies for the patients who need them.
Senior Quality Assurance Specialist
This position performs compliance assessments of site and cross-site quality systems, including process inspections, facility inspections, record review, computer validation, and training records. He/she provides recommendations for improvements in auditing quality systems based on knowledge and understanding of current regulatory inspection guidance and internal trends.
The ideal candidate will possess a bachelor’s degree, preferably in a life science. He/she will have a minimum of five years of experience in a quality assurance role. The person will have experience with Microsoft Office applications, including Access and Excel. He/she must have RQAP certification.
Click here to read more about the Senior Quality Assurance Specialist position at Charles River.
This position operates and troubleshoots a variety of instruments and equipment for pharmaceutical sample testing, including HPLC/UPLC, GC, FTIR, UV, and more. He/she documents test results in lab notebooks, in real time, and communicates the status of test results to supervisors. The person conducts peer review of lab notebooks for technical details.
The ideal candidate will possess a bachelor’s degree in chemistry with at least five years of related experience, a master’s degree with at least two years of related experience, or a Ph.D. with up to two years of related experience. He/she will have knowledge of experiment documentation, operation, and basic troubleshooting. The person will have knowledge of chemical concepts and theories, and be familiar with a variety of lab equipment and data acquisition.
Click here to read more about the Analytical Scientist position at Charles River.
This position cleans GMP processing rooms and associated areas, while maintaining cleaning logs according to established procedure. He/she cleans equipment after use, moves clean equipment to storage, maintains the equipment log, and keeps clean equipment organized. The person assembles and sets up equipment per MBR and the formulator’s request.
The ideal candidate will possess an associate degree or high school diploma. He/she will have up to three years of industry experience cleaning, preparing, and working with pharmaceutical equipment. The person will preferably have experience with equipment, troubleshooting, warehousing, and manufacturing in a cGMP environment.
Click here to read more about the GMP Custodian position at Charles River.