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Quality Program Associate

Barcelona💼 Full-time🗓 2026-06-10 → 2026-07-31

Core

Support the delivery of GxP software solutions into highly regulated pharmaceutical manufacturing environments by building and maintaining quality programs for customer implementation projects.

Role type

Quality Program Associate (early-career)

Builds

GxP-compliant software implementations for pharma manufacturers

Domain

Life sciences / Pharmaceutical manufacturing / Quality Assurance

Deliverable

client delivery

Required skills

Computer System Validation (CSV/CSA), quality planning, documentation management, inspection readiness, GMP compliance knowledge

Preferred skills

None stated

Technologies

None stated

Responsibilities

Support quality planning and computer system validation (CSV/CSA) for customer projects, maintain quality programs for implementation projects, ensure projects meet GMP and regulatory expectations, prepare documentation for inspections

Seniority

Early-career, hands-on IC

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