Quality Assurance Specialist - GMP Compliance


Madrid
Contract
Negotiable
Quality
CR/560912_1758090414
Quality Assurance Specialist - GMP Compliance

Quality Assurance Specialist - GMP Compliance

Location: Madrid or remote within Spain/Portugal
Employment Type: 6-month contract

We are currently supporting a leading pharmaceutical company in expanding its Quality Assurance team. This role is ideal for professionals with hands-on experience in GMP compliance, deviation investigations, and batch documentation review, who are passionate about maintaining high standards in regulated environments.

Key Responsibilities:

  • Investigate deviations, perform root cause analysis, and manage CAPA implementation
  • Review and approve GMP documentation for packaging, inspection, and conditioning processes
  • Support internal audits, regulatory inspections, and SOP updates
  • Collaborate with cross-functional teams to ensure quality system compliance
  • Contribute to continuous improvement initiatives within the QA department

Candidate Profile:

  • 1-3 years of experience in Quality Assurance within a GMP-regulated pharmaceutical setting
  • Strong understanding of CAPA management, documentation control, and compliance standards
  • Familiarity with systems such as LIMS, SAP, and GxP Suite
  • Degree in Pharmacy, Life Sciences, or a related field
  • Fluent in Spanish; English proficiency required

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