Quality Engineer (Temporary Contract)

Actual Talent is the talent acquisition consultancy that offers Executive Search, RPO and Talent Solutions.

Our purpose is to drive the growth and fulfillment of individuals and organizations. We facilitate individuals in finding inspiring opportunities and help organizations discover professionals who will take them to the next level. We do this through talent acquisition and development solutions that focus on people, diversity and inclusion, innovation, and cutting-edge technology.

About the client:

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

The mission of this position is to guarantee that the Standards under which the Quality System is based are aligned with the requirements of the different Regulations of the Countries and Organizations where the company sells the products. Additionally, you will assure that all products manufactured are designed, manufactured and released according to established procedures.

This role will work with specific manufacturing teams to drive continuous improvement of Quality within manufacturing seeking defect rate reduction, increased manufacturing efficiency, reduced costs and enhanced customer satisfaction.

Main Responsabilities

Change Management: Evaluate the impact of the proposed changes and management of change control.

Review and approval of manufacturing and general procedures.

Validation: Establish a strategy to validate changes, and review and approve validation strategies and the corresponding documentation (protocol and report).

Risk Assessment: Perform, review, and approve the risk assessment performed to evaluate the impact of changes and non-conformances in the final product.

Management of Non-Conformities and CAPA.

Develop a Quality Improvement plan for the manufacturing area of responsibility.

Measurement and reporting of Quality KPIs and metrics for the manufacturing area of responsibility.

Participate in Internal and External Audits.

Perform Quality Training to all personnel.

Review of product Batch Record as needed.

Requirements

Education: Bachelor's degree (Diplomatura) in Chemistry, Biotechnology or other Sciences. (Degree may be substituted by relevant skills and work experience).

Experience: 3 years in a similar position.

Standards: Knowledge of Quality standards.

Languages: Fluency in Spanish or Catalan. Advanced knowledge of English (reading and speaking).

Software: Fluency in Office Tools (Excel & Word). Basic knowledge in SAP is valuable.

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.