Técnico/a Validaciones

Souhaitez-vous rejoindre une équipe internationale qui travaille à l'amélioration des soins de santé ? Voulez-vous améliorer la vie de millions de personnes ? Grifols est une entreprise mondiale de soins de santé qui, depuis 1909, travaille à l'amélioration de la santé et du bien-être des personnes dans le monde entier. Nous sommes leaders dans le domaine des médicaments dérivés du plasma et de la médecine transfusionnelle et nous développons, produisons et commercialisons des médicaments, des solutions et des services innovants dans plus de 110 pays et régions.

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 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 people. That's why we need a Technical Validationslike you.

Role Mission

In the Validations Department at Instituto Grifols, we need to recruit an Equipment and Process Validation Technician. Their primary role will be to manage and execute assigned validation projects in accordance with current regulations, ensuring the validity of production processes.

What your responsibilities will be

• You will draft, review, and approve qualification protocols and reports.
• You will draft, review, and approve validation protocols and reports.
• You will execute qualification and validation studies.
• You will update validation protocols to comply with current regulations.
• You will edit deviations, monitor CAPAs, and assess change controls.

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).

• Degree in Engineering or a Bachelor's degree in Health Sciences is a plus, a Master's degree in the Pharmaceutical and Parapharmaceutical Industry is a plus.
• You have 1 to 3 years of experience working in a similar position.
• You have an advanced level of English (minimum B2.2).
• You are proficient in the Office suite and have basic SAP user skills.
• You are available to travel on an ad hoc basis.

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 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

Grifols is an equal opportunity employer.

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Flexible schedule: Monday-Thursday 8:00h – 17:00h and Friday 8:00h 15:00h.

Benefits package

Contract of Employment: Permanent position

Flexibility for U Program: 1 day remote working

Location: Parets del Vallès

Learn more about Grifols