Scientist New Process Development, Cmc

¿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.**

From the Scientific Innovation Office at Grifols we are looking for a Scientist R&D - Process Development, to join to the New Process Development Division within CMC.

Specifically, the main mission of the Process Development group is the design and development of new protein purification processes for obtaining new products or for improving the existing ones.

A qualified biotech scientist in the area of Bioscience is requested with the aim to manage Bioprocess development projects in a highly flexible, rigorous and multidisciplinary area.

**What your responsibilities will be**:

- Design and develop new protein purification processes for obtaining new products or improving the existing commercial ones.
- Qualify the developed processes at higher scale in order to check the robustness and consistency of the new processes, in accordance with Safety and Quality guidelines.
- Prepare and rationale Study desings and Bioprocess work orders so that to ensure that they are executed with good performance and accordingly to the project goals.
- Subsequent assessent of the results obtained in the experimental process, integrating the results in the global project objective.
- Prepare the development reports and presentations for the R&D management, accepting responsibility for them.
- Prepare technical documentation for dossiers requested by Regulatory areas, supporting the new product licenses.
- Prepare general R&D documentation, related to intellectual property, equipment data integrity, Quality compliance, laboratory procedures (SOP), etc.
- Investigate new purification technologies in order to be aligned with the Bioprocess state of the art and optimize our current methods.

**Who you are**:

- You have a degree in Pharmaceutical Industry or similar (biotechnology, biochemistry, chemist, etc.). An specific Bioprocess PhD. or equivalent experience in bioengineering or pharma related areas will be valued.
- You speak fluent English, as you will be managing international projects.
- You are communicative and proactive to facilitate and strength team workstreams.
- You are analytical and with strong ability to design and verify hypotheses, in a flexible and scientific-based environment.
- You are able to manage projects under a highly demanding Grifols Quality System.

**What we offer**:

- Permanent position.
- Benefits package.
- Flexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time).

This 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.

Grifols is an equal opportunity employer.

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**Ubicación**:SPAIN : España : Parets del Valles**:cust_building**

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