STERIS is a leading provider of infection prevention and procedural products and services for healthcare, pharmaceutical, and medical device customers. With a focus on innovation and safety, the company offers a wide range of solutions including sterilization technologies, contamination control, and endoscopy equipment. STERIS aims to create a healthier world by delivering world-class products and services globally, while fostering a great workplace culture that values its 17,000 associates worldwide.
The QC Laboratory Supervisor is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards. This position is responsible for all aspects of quality control within the organization including receiving, in-process, finished goods testing, scheduling resources, defining solutions to improve compliance, and provide key input to senior management on compliance in accordance with the requirements for ISO, FDA QSR, and STERIS policies.
STERIS is a leading provider of infection prevention and procedural products and services for healthcare, pharmaceutical, and medical device customers. With a focus on innovation and safety, the company offers a wide range of solutions including sterilization technologies, contamination control, and endoscopy equipment. STERIS aims to create a healthier world by delivering world-class products and services globally, while fostering a great workplace culture that values its 17,000 associates worldwide.