Validations Engineer

Actual Talent; Barcelona; Híbrido; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

A global innovative company in Barcelona is seeking a Quality Validation professional who will ensure that all products meet quality standards. The role includes responsibilities such as reviewing manufacturing procedures and participating in audits. The candidate should have a Bachelor's degree in Biotechnology and at least 3 years of experience in a relevant field. The position offers a hybrid work model and a competitive benefits package.

Servicios

Health insurance

Pension plan

On-site cafeteria

Parking

Professional development programs

Formación

• Minimum 3 years of experience in a validation role within pharmaceuticals or similar industry.
• Advanced English and fluent in Spanish or Catalan.

Responsabilidades

• Review and approve manufacturing procedures and technical changes.
• Evaluate the impact of proposed process/product changes.
• Participate in internal and external audits.

Conocimientos

Knowledge of quality and validation standards

Teamwork

Time management

Detail-oriented

Educación

Bachelor’s degree in Biotechnology or related field

Herramientas

MS Office (Excel, Word)

SAP

Descripción del empleo

About the client

Werfen is a global leader in specialized diagnostics operating directly in over 30 countries and reaching more than 100 territories worldwide through distributors.

We develop, manufacture and distribute integrated solutions including systems, reagents, automation and software for use primarily in hospitals and clinical laboratories.

At Werfen we are driven by innovation, precision and collaboration. Our people are at the heart of everything we do, 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 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.

Employment Type: Full Time

Experience: 3+ years

Vacancy: 1