¿Te gustaría unirte a un equipo internacional que trabaja para mejorar el futuro del sector de la salud? ¿Quieres contribuir a mejorar la vida de millones de personas? Grifols es una compañía global del sector de la salud que desde 1909 mejora la salud y el bienestar de las personas en todo el mundo. Somos líderes en medicamentos hemoderivados y medicina transfusional y desarrollamos, producimos y comercializamos medicamentos, soluciones y servicios innovadores en más de 110 países y regiones.

We believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunity fostering an inclusive environment where diversity makes us be 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 Quality Systems Specialist like you.

Mission

Within the Global Biopharma Quality & Regulatory Compliance department of Grifols, S.A., we are looking for a Quality Systems Specialist. The Quality Systems Specialist will support the Global Biopharma Quality & Regulatory Compliance department in maintaining and improving the quality management system (QMS) to ensure compliance with regulatory requirements and industry standards. This role involves monitoring, maintaining, and enhancing quality processes, documentation, and systems to ensure the highest standards of product quality and safety. The Quality Systems Specialist will also participate in and coordinate global projects, ensuring consistent quality standards across all regions, and coordinate multidisciplinary working groups from different regions.

What your responsibilities will be

• Develop and implement global procedures to standardize quality processes across all regions

• Work closely with global teams to align quality processes and standards.

• Participate in and coordinate global quality projects, ensuring consistent application of quality standards across all regions.

• Evaluate suppliers, monitor supplier quality issues, and coordinate failure investigations. Create reports on supplier performance.

• Coordinate multidisciplinary working groups from different regions to ensure standardization of quality strategies.

• Analyze new regulations and ensure compliance across all regions.

• Assist in the revision process validation activities to ensure manufacturing processes meet quality standards.

Who you are

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions)

• Bachelor's degree in a relevant field (e.g. Life Sciences, Quality Management).

• Minimum of 5 years of experience in quality assurance within the pharmaceutical industry

• Strong knowledge of regulatory requirements.

• Excellent technical writing and documentation skills.

• Experience in managing global projects and coordinating with international teams.

• Proven ability to develop and implement global procedures.

• Ability to analyze and interpret new regulations.

• Ability to effectively communicate with internal and external stakeholders across different regions.

• Strong focus on accuracy and thoroughness in all tasks.

• Ability to identify issues and implement effective solutions.

• Collaborative approach to working with colleagues and other departments globally

· 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. If you are interested in joining our company and you have what it takes for such an exciting position, then don’t hesitate to apply!

We look forward to receiving your application!

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.

Flexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h.

Benefits package

Contract of Employment: Permanent position

Flexibility for U: 2 days remote working

Location: Sant Cugat del Vallès

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Ubicación: SPAIN : España : Sant Cugat del Valles : [[cust_building]]

Conoce más sobre Grifols (http://www.grifols.com/es/web/international/home)

Req ID: 527674

Type: Indefinido tiempo completo

Job Category: AREA TECNICA OPERACIONAL