Myant is seeking a Quality Engineering Specialist to strengthen manufacturing processes, supplier quality and QMS compliance in a regulated medical device setting. You will work cross‑functionally to support risk‑based decision making and continuous improvement across design transfer, production, CAPA and supplier qualifications.
The role requires hands‑on quality engineering within medical devices, with experience implementing ISO 13485, ISO 14971, and related standards, and leading pFMEA,