¿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 opportunities that foster an inclusive environment.

Help us lead one of the world's largest pharmaceutical companies. We are a world leader in plasma-derived medicines with 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.

Role Mission

Collaborate in the implementation and maintenance of the Quality System in accordance with applicable regulations for products manufactured and/or marketed by Laboratorios Grifols to ensure that they possess the quality required for their intended use.

What your responsibilities will be

• Collaborate in the implementation of the Quality System.
• Participate in the evaluation of standards, guidelines, and other relevant documents, in accordance with applicable regulations.
• Collaborate in the review and analysis of external regulations that impact the Quality System.
• Collaborate in monitoring action plans and liaise with the relevant departments.
• Participate in conducting process/facility and Quality System risk assessments.
• Participate in external and/or customer audits.
• Collaborate in Quality System training, as well as in the review of processes that impact the Quality System.
• Participate in Quality System document review workflows using the electronic Document Management system.
• Promote document harmonization across manufacturing plants.
• Conduct follow-up meetings with the relevant departments.
• Maintain process indicators.
• Collaborate in maintaining the document archive.

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 biology, Chemistry, Pharmacy, Biotechnology or similar.
• English level B2. (Essential).
• You have minimum 1 year of experience in a similar position within the pharmaceutical industry.
• SAP experience (Valuable)
• Master's degree in health sciences or master's degree in quality or knowledge of quality in the pharmaceutical industry and performance of Risk Analysis (Valuable)
• You are a dynamic, proactive person who can carry out projects independently with a sense of responsibility. You are organized and methodical, and you enjoy working in a team.

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!

Grifols is an equal opportunity employer.

Flexible schedule:Monday-Thursday 7:00-10:00 a 16:00-19:00h and Friday 8:00 -15:00h.

Contract of Employment: Regular Full-Time

Location: Parest del Vallès

www.grifols.com

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