Senior CSV Validation Engineer - Pharma industry
OntarioContrat
A
ALGOBRAINZ
6+ ansCandidates need 6+ years of computer systems validation experience in GMP pharmaceutical settings, including building management or control systems. They must know GAMP 5, 21 CFR Part 11, FDA and EMA expectations, and data integrity principles.
Johnson Controls Metasys, AVEVA PI Historian, DeltaV, OPC UA
QMS, Investigations & CAPA SME
OntarioContrat
A
ALGOBRAINZ
5+ ansCandidates need at least 5 years of pharmaceutical quality experience, including deviation investigations, root-cause analysis and technical writing. Hands-on work with electronic QMS platforms such as TrackWise, Veeva Vault QMS or MasterControl is preferred.
TrackWise, Veeva Vault QMS, MasterControl