Katalyst CRO is hiring a QMS Consultant to evaluate and improve medical device manufacturers' Quality Management Systems (QMS). This role involves planning and leading mock audits to ensure compliance with ISO 13485:2016 and EU regulations.The ideal candidate will have at least 8 years of experience in the Medical Device industry and hold ISO 13485 Lead Auditor certification. Excellent communication skills are essential as the role requires working under tight timelines with senior leadership.#J-18808-Ljbffr
| Location | Manchester, NH |