About this role
Quality Specialist at LGC Group. Location: Kidlington, United Kingdom. Role: enhancing quality, conducting audits, maintaining documentation Requirements: BSc in science/engineering/QA, minimum 3 years quality experience in medical device/pharmaceutical/biotech/lab, strong ISO 9001 knowledge, familiarity with ISO 13485/14971, auditing experience, strong communication and attention to detail. Category: Quality Assurance Seniority: Mid Level Commitment: Full Time Workplace: Onsite Languages: English