2 of 2 21 CFR Part 11 Jobs in Slough

pharmaceutical manufacturing environment Veeva Vault experience highly desired Proficiency with DMS (D2) or similar electronic document management systems Strong understanding of GMP regulations (21 CFR Part 11, EU Annex 11), and pharmaceutical documentation requirements Exceptional attention to detail, organizational, and time-management skills Strong interpersonal ...

Sciences or related field 3+ years in document control within GMP pharma Experience with DMS (D2 or similar systems) Strong knowledge of GMP (e.g., 21 CFR Part 11, EU Annex 11) Excellent organisation and communication skills Why apply? Join a collaborative global team and play ...