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Actalent • Barcelona, Catalonia, Spain
Role & seniority
Stack/tools
Top 3 responsibilities
Review and approve manufacturing procedures and technical changes; assess impact of proposed process/product changes (Change Management).
Lead/execute validations and qualifications (facilities, equipment, utilities, processes, FAT/SAT) and perform risk assessments.
Manage deviations, non-conformities, CAPAs; participate in internal and external audits; provide training on validation and risk management; drive continuous quality improvements.
Must-have skills
Bachelor’s degree in Biotechnology, Life Sciences, or related field.
≥3 years in a validation role within pharma/biotech or similar industry.
Strong knowledge of quality and validation standards; methodical, organized, detail-oriented; effective teamwork and time management.
Proficiency with MS Office; advanced English (written/spoken); Spanish or Catalan fluency.
Nice-to-haves
SAP experience beyond basics; direct experience with FAT/SAT and GMP-compliant validation projects.
Experience delivering training and contributing to Quality System robustness and continuous improvement.
Location & work type
Hybrid work model: 3 days onsite + 2
Hybrid work model: 3 days onsite + 2 days remote.
Competitive benefits package: health insurance, pension plan, on-site cafeteria, parking, and professional development programs. A chance to grow within a global, innovative company driving diagnostic excellence. If you’re passionate about Quality, Validation, and continuous improvement, we’d love to hear from you! Apply now or get in touch to learn more about this opportunity.