About the company: Our client is a global leader in
specialized diagnostics, operating directly in more than 30
countries and reaching over 100 territories worldwide through
distributors. They develop, manufacture, and distribute integrated
diagnostic solutions — including systems, reagents, automation, and
software — primarily for hospitals and clinical laboratories.
Driven by innovation, precision, and collaboration, their teams are
committed to advancing patient care through excellence in science
and technology. Your Mission Ensure that all products manufactured
by our OEM partners are designed, produced, and released according
to established procedures, validated processes, and quality
standards. You will also contribute to strengthening Werfen’s
Quality System through continuous improvement initiatives. Main
responsibilities Review and approve manufacturing procedures and
technical changes. Evaluate the impact of proposed process/product
changes ( Change Management ). Review and execute validations and
qualifications (facilities, equipment, utilities, processes,
FAT/SAT). Perform and approve Risk Assessments . Participate in
internal and external audits. Manage deviations, non-conformities,
and CAPAs.



Provide training in validation and risk management to
internal staff. Propose and implement improvements to enhance
Quality System robustness and best practices. Requirements:
Bachelor’s degree in Biotechnology, Life Sciences, or a related
field. Minimum 3 years of experience in a validation role within
the pharmaceutical, biotech, or similar industry. Strong knowledge
of quality and validation standards. Proficiency in MS Office
(Excel, Word); basic SAP knowledge is a plus. Advanced English
(spoken and written); fluent in Spanish or Catalan. Methodical,
organized, detail-oriented, with strong teamwork and time
management skills. What we offer: Join a young and collaborative
team in an international environment. 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
general, 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.

📌 Validations Engineer (Cataluña)
🏢 Actual Talent
📍 Cataluña