About this role
Quality Engineer, Validation at OrganOx. Location: Oxford, England, United Kingdom. Role: leading validation, analyzing data, supporting suppliers Requirements: Process and test method validation experience in a regulated industry (medical devices preferred); writing VMP/IQ/OQ/PQ/VSR and GR&R; pFMEA and risk-based decision making; supplier validation and statistical analysis; degree in bioscience/engineering or equivalent. Category: Engineering Seniority: Mid Level Tools: ISO 13485, FDA 21 CFR Part 820, FDA 21 CFR Part 11, Gage R&R, MSA, pFMEA Commitment: Full Time Workplace: Onsite Languages: English