Master Data Engineer
Core
Managing and maintaining Master Data objects within Laboratory Information Management Systems (LIMS) for a global pharma/biotech organization.
Role type
Master Data Engineer (Regulatory/LIMS)
Builds
LIMS master data objects, sampling plans, and LES worksheets
Domain
Pharmaceutical/Biotech / Quality Control / Regulatory Compliance
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
LIMS administration, GxP compliance, document management, data collection and review, corrective action planning, user support, regulatory requirements knowledge
Preferred skills
Labvantage experience, HPLC laboratory experience, eQMS familiarity
Technologies
LIMS, Labvantage, eQMS, LES
Responsibilities
Create and update LIMS master data objects including specs and sampling plans; Collect and review data from QC departments for LIMS implementation; Troubleshoot and resolve user support tickets; Create, edit, and route documents for compliance approval; Recommend corrective actions and develop best practices; Review data in accordance with GxP procedures; Train analysts on LIMS usage; Support document revision, CAPA, and investigation tasks.
