Manufacturing & Process Validation Specialist B

hace 2 semanas

Madrid, Madrid, España Grifols A tiempo completo


¿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 people. That's why we need a Manufacturing & Process Validation Specialist like you.

Role Mission

In the Validations Department at Progenika Biopharma, 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.

Flexible schedule: Monday-Thursday 8:00h – 17:15h and Friday 8:00h 14:00h.

Benefits package

Contract of Employment: Temporary Full-Time

Flexibility for U Program: Occasionally remote

Ubicación: SPAIN : España : Derio:[[cust_building]] 

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