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Quality Assurance Consultant

Ullastrell, Barcelona💼 Full-time🗓 2026-04-01 → 2026-09-23

Core

Support batch review, release, and regulatory compliance for pharma, biotech, and medical device clients across the product lifecycle.

Role type

Quality Assurance Consultant (GMP)

Builds

Quality systems, batch documentation, and regulatory compliance artifacts for life sciences clients

Domain

Life Sciences (Pharma, Biotech, Medical Devices)

Required skills

GMP compliance, batch review, sterile manufacturing knowledge, regulatory documentation, deviation/CAPA management, audit support

Preferred skills

Industrial Pharmacist background, stakeholder communication, problem-solving

Technologies

GMP documentation systems, sterile manufacturing environments

Responsibilities

Support batch review and release, interpret GMP documentation, work on deviations and CAPAs, support audits and inspections

Seniority

Mid-level, hands-on IC

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