Quality Engineer (Temporary Contract)

Werfen Immunoassay; Madrid; Híbrido; EUR 35.000 - 50.000; Jornada completa

Descripción de la vacante

A leading diagnostics company seeks a Quality Manager to ensure compliance with regulatory standards and drive improvements in manufacturing efficiency. This role requires a Bachelor’s degree in Chemistry or related fields and 3 years of experience. Candidates should be fluent in Spanish or Catalan, with advanced English skills. The position offers a hybrid work model and a competitive benefits package, including health insurance and professional development opportunities.

Servicios

Health insurance

Pension plan

On-site cafeteria

Parking

Professional development programs

Formación

• 3 years experience in a Quality Management role or similar position.
• Knowledge of Quality standards applicable to manufacturing.
• Fluency in Spanish or Catalan and advanced English (reading and speaking).

Responsabilidades

• Ensure quality standards align with regulatory requirements.
• Drive continuous improvement of quality and manufacturing efficiency.
• Review and approve manufacturing procedures and documentation.
• Manage non-conformities and develop Quality Improvement plans.

Conocimientos

Methodical and well-organized

Teamwork

Time management

Decision-making under pressure

Educación

Bachelor's degree in Chemistry, Biotechnology, or other Sciences

Herramientas

Office Tools (Excel & Word)

SAP

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.

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 Biokit sells the products. Additionally, you will assure that all products manufactured at Biokit 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 Responsibilities

• Review and approval of manufacturing and general procedures.
• Change Management: Evaluate the impact of proposed changes and manage change control.
• Validation: Establish 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 at Biokit 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; measure and report Quality KPIs and metrics; participate in internal and external audits; perform quality training for all personnel; review product batch records 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.

Skills & Capabilities

• Methodical and well‑organized.
• Teamwork and the ability to collaborate actively with working groups.
• Time management skills and ability to make decisions under pressure.
• Ability to apply a systematic approach and constant control, follow‑up and verification of the results.

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.

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

Apply now or get in touch to learn more about this opportunity.