About this role
QMS Specialist at Smithnephew. Location: Hull or United Kingdom. Role: supporting QMS, supporting audits, analyzing data Requirements: Quality Assurance experience in medical device or pharmaceutical industry with knowledge of ISO 13485, MDR, FDA 21 CFR Part 820; experience with QMS processes (CAPA, document/change control, training, nonconformance, audits); data analysis and stakeholder engagement skills. Category: Quality Assurance Seniority: Mid Level Commitment: Full Time Workplace: Hybrid Languages: English