Scientist New Process Development

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.

From the Scientific Innovation Office at Grifols, we are looking for a Scientist R&D - Process Development to join 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 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 Quality guidelines.
• Prepare and rationale Study designs and Bioprocess work orders so that to ensure that they are executed with good performance and accordingly to the project goals.
• Subsequent assessment 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.

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.

• You have a degree in Pharmaceutical Industry or similar (biotechnology, biochemistry, chemistry, etc.). A specific Bioprocess PhD or equivalent experience in bioengineering or pharma related areas will be highly valued.
• You speak fluent English, as you will be managing international projects.
• You are communicative and proactive to facilitate and strengthen team workstreams.
• You are analytical and have a 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

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 8h to 17h and Friday 8-15h.

Benefits package

Contract of Employment: Permanent position

Flexibility for U Program: Hybrid

Location: Parets del Vallès

Location: SPAIN : España : Parets del Valles:[[cust_building]]