Responsibilities. Responsible for validation programs in support of GMP manufacturing. Responsible for facility, utility and equipment qualification programs. Responsible for QA role in process and assay validation programs. Review or author validation related documents such as design specification, URS, FAT, SAT, IQ, OQ, PQ for utility and equipment. Assume QA lead role in software validation. Maintain and update validation master plans. Execute...
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 tha...
My client, NewCo is building their team. This is an exceptional opportunity to join an early-stage company and work with an outstanding and collaborative team engaged in innovative approaches in the immunology field. We are seeking a highly motivated senior research associate to join our discovery group. The candidate should have technical proficiency in various immunological and ex vivo pharmacology assays. We are seeking collaborative individua...
Research Associate I. Location. Lexington, MA. Details. On-site, 5 days/week (in Lab). Job Description. Join our multinational and diverse team as a Research Associate in the Nucleic Acid Delivery, Formulations & Bioanalysis department. Collaborating with Laboratory Technicians, Specialists/Scientists, and a global department manager, you will contribute to the development of synthetic/non-viral nanomedicines, employing advanced analytical charac...
