IVD Systems Engineering Specialist

Grifols; Parets del Vallès; Híbrido; EUR 48.000 - 60.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Hybrid work model

Flexible schedule

Permanent position

Descripción de la vacante

Grifols, a global healthcare leader, seeks a Systems Engineering Specialist to join the IVD Systems Department in Parets del Vallès. The role focuses on defining and validating system specifications, ensuring traceability, and aligning with regulatory and quality requirements.

You will lead cross-functional reviews, document architectures, and drive risk analyses within an Agile framework, contributing to compliant, robust solutions in a regulated setting.

Formación

• University degree in Engineering, Systems Engineering, Electronics, Computer Science, Biotechnology or related field.
• 2–5 years of professional experience in technical roles related to systems engineering, product development or complex technologies.
• Advanced level of English, both written and spoken.

Responsabilidades

• Define, coordinate, oversee and document product and system specifications aligned with functional, regulatory, manufacturing and quality requirements.
• Ensure the consistency, completeness and traceability of specifications throughout the system lifecycle.
• Lead and coordinate technical reviews of specifications with all relevant stakeholders.
• Define, coordinate and document system architectures that meet approved requirements and specifications.
• Ensure technical consistency between requirements, architecture, and implementation constraints.
• Participate in technical decision-making to ensure feasibility of solutions.
• Define, execute and document tests and analyses to evaluate feasibility of system solutions.
• Design and define test setups for feasibility studies.
• Analyze results and ensure proper documentation and traceability.
• Lead and participate in risk analysis reviews for IVD systems.
• Identify improvement actions and monitor their implementation.
• Lead cross-functional meetings on system definition, feasibility and integration.
• Develop work procedures and technical instructions for department activities.
• Organize and prioritize team activities using Agile methodologies.

Conocimientos

Systems Engineering

Technical documentation

Risk analysis

Agile methodologies

English proficiency

Educación

Engineering degree

Herramientas

Office productivity tools

Document management systems

Descripción del empleo

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

We believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities, fostering an inclusive environment where diversity makes us outstanding.

Help us lead one of the world’s largest pharmaceutical companies. We are a world leader in plasma-derived medicines with a presence in more than 100 countries, and a growing global team of over 20.000 people. That’s why we need a Systems Engineering Specialist like you to join IVD Systems Department of the Instrument Development & Life Cycle Management (LCM) Area at Diagnostic Grifols S.A.

The Systems Engineering team is responsible for ensuring the technical consistency, feasibility and end-to-end integration of IVD systems, guaranteeing alignment with functional, regulatory, manufacturing and quality requirements to develop robust and compliant solutions.

What Your Responsibilities Will Be

• Define, coordinate, oversee and document product and system specifications aligned with functional, regulatory, manufacturing and quality requirements.
• Ensure the consistency, completeness and traceability of specifications throughout the entire system lifecycle.
• Lead and coordinate technical reviews of specifications with all relevant stakeholders.
• Define, coordinate and document system architectures that meet approved requirements and specifications.
• Ensure technical consistency between requirements, architecture, and implementation constraints.
• Participate in technical decision-making processes to ensure the robustness and feasibility of proposed solutions.
• Define, coordinate, execute and document the tests and analyses required to evaluate the feasibility of system solutions.
• Design and define test setups and configurations required for feasibility studies.
• Analyze results and ensure proper documentation and traceability.
• Lead and participate in risk analysis reviews for IVD systems.
• Identify, analyze and propose corrective and improvement actions, monitoring their implementation and effectiveness.
• Lead cross-functional meetings related to system definition, feasibility and integration.
• Develop work procedures and technical instructions to ensure the proper execution of departmental activities.
• Organize and prioritize team activities using Agile methodologies, promoting the adoption of these ways of working.
• Ensure that all documentation related to assigned activities is accurate, complete and kept up to date.
• Apply and promote compliance with Quality System procedures.

Who You Are

• University degree in Engineering, Systems Engineering, Electronics, Computer Science, Biotechnology, Health Sciences or a related field.
• Between 2 and 5 years of professional experience in technical roles related to systems engineering, product development or complex technologies.
• Advanced level of English, both written and spoken.
• Strong knowledge of Systems Engineering principles applied to complex and regulated products.
• Ability to define and analyze system behavior, interfaces and technical constraints.
• Experience with technical documentation, traceability and structured problem analysis.
• Knowledge of risk analysis and risk management in regulated environments.
• Ability to translate functional, regulatory, and quality requirements into technical specifications.
• Familiarity with Agile methodologies in engineering or product development environments.
• Proficiency in office productivity tools and technical document management systems.

What We Offer

It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.

Information about Grifols is available at www.grifols.com.

We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help.

Grifols is an equal opportunity employer.

Flexibility for U Program:

Hybrid

Flexible schedule:

Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time).

Benefits Package

Contract of Employment:

Permanent position

Location:

Parets del Vallès

Location: SPAIN : España : Parets del Valles:[[cust_building]]

www.grifols.com

Learn more about Grifols