Description: Quality System requirements, cGMP, FDA and ISO 13485 standards. Areas of responsibilities include receipt and review of documents such as charts, logs, batch records…
Description Manages budgets for federal and non-federal research grants, contracts and sub-contracts. Partners with the Office of Sponsored Programs to maintain databases for pen…
Description Manages budgets for federal and non-federal research grants, contracts and sub-contracts. Partners with the Office of Sponsored Programs to maintain databases for pen…
Description: Working under the direction of the Lab Manager, the lab assistant is responsible for the registration and processing/accessioning of specimens according to approved …
Description: The Regulatory Affairs Specialist is responsible for identifying, evaluating, and ensuring compliance with all applicable laws, regulations, and standards. The Regul…
Description: Position Summary: The Clinical Trial Lead (CTL) / Study Lead will establish, track and deliver clinical operations milestones The CTL / Study Lead will provid…
Description: Review and release batch records following GMP Author or edit SOPs Support investigation, CAPA, and audit efforts Assist chemists with raw materials and recording…
Description: Primary Activities: Assist study leads with combination drug-device assembly and test sample preparation. Coordinate gamma irradiation runs (at 3rd party vendor)…
Description: Assist study leads with combination drug-device assembly and test sample preparation. Coordinate gamma irradiation runs. Assist study leads with in vitro release s…
Description: Quality System requirements, cGMP, FDA and ISO 13485 standards. Areas of responsibilities include receipt and review of documents such as charts, logs, batch records…
Responsibilities Ensures equipment in exam rooms is working each morning, e.g., otoscopes, blood pressure cuffs, etc. Maintains general appearance and cleanliness of examina…
Description: Position Overview: We are seeking a highly skilled Production Planner to join our dynamic team. The Production Planner will be responsible for overseeing the plannin…
Description: Review and release batch records following GMP. Author or edit SOPs. Support investigation, CAPA, and audit efforts. Assist chemists with raw materials recordkeep…