Quality Systems Engineer

Werfen Immunoassay; Madrid; Híbrido; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

A global leader in diagnostics located in Madrid is seeking a Quality Manager to ensure adherence to quality standards and drive continuous improvement in manufacturing. Candidates should possess a Bachelor’s degree in Chemistry, Biotechnology, or related fields, with fluency in Spanish or Catalan, and advanced English skills. This role entails reviewing manufacturing procedures, managing change controls, and conducting quality training. A competitive benefits package is offered along with a flexible hybrid work model (3 days onsite, 2 days remote).

Servicios

Health insurance

Pension plan

On-site cafeteria

Parking

Professional development programs

Formación

• Bachelor's degree in Chemistry, Biotechnology or related field.
• Fluency in Spanish or Catalan; advanced English required.
• Ability to use Office tools proficiently.

Responsabilidades

• Review and approve manufacturing and general procedures.
• Evaluate impact of proposed changes and manage change control.
• Develop a Quality Improvement plan for manufacturing.

Conocimientos

Knowledge of Quality standards

Fluency in Spanish

Fluency in Catalan

Advanced English (reading and speaking)

Fluency in Office Tools (Excel & Word)

Basic knowledge in SAP

Educación

Bachelor's degree (Diplomatura) in Chemistry, Biotechnology or other Sciences

Descripción del empleo

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.

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 Biokit sells the products. 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.

Review and approval of manufacturing and general procedures.

Change Management

• Evaluate the impact of the proposed changes and management of change control.
• 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.

Perform Quality Training to all personnel at Biokit.

Qualifications and Skills

Bachelor's degree (Diplomatura) in Chemistry, Biotechnology or other Sciences. (Knowledge of Quality standards.

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.

Ability to apply a systematic approach and constant control, follow-up and verification of the results.

Hybrid Work Model

3 days onsite + 2 days remote.

Competitive Benefits Package

Health insurance, pension plan, on-site cafeteria, parking, and professional development programs.

If you’re passionate about Quality and continuous improvement, we’d love to hear from you!