We don't treat pharma recruitment as one bucket. Every function has its own regulatory language, employer expectations, and sponsorship patterns — so our matching works differently for each.
Batch record review, deviations and CAPA ownership, QMS administration, audit hosting and readiness across GMP-regulated sites.
Analytical and microbiological testing, method validation and transfer, stability studies, lab compliance and instrument qualification.
Dossier compilation and submission, MHRA/EMA liaison, labelling compliance, variations and lifecycle registration maintenance.
Trial monitoring and site management, CRA and CRO-side roles, GCP compliance, clinical trial documentation and TMF management.
Individual case safety report processing, signal detection support, safety database management, PSUR and aggregate reporting.
Production and process engineering, tech transfer, cleaning & process validation, and GMP site operations support.