table.MiTabla { max-width: 1020px;!important

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 opportunities that foster an inclusive environment.

The mission of the role will be to be responsible for leading and managing bioprocess development projects within a highly flexible, rigorous, and multidisciplinary environment. The role will focus on designing, optimizing, and scaling up purification processes for plasma-derived proteins, either for the development of new therapeutic products or for the improvement of existing ones.

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 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 and technical 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

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 or Master’s degree in biotechnology or chemistry engineering (or equivalent).
• Experience in a similar position in the pharmaceutical or biotechnology industry will be valued.
• Advanced level of English, minimum C1 required. Most projects are managed in English.
• Positive attitude, capacity to learn new abilities and knowledge and ability to work in a team.
• Good communication skills.
• Analytical and accuracy skills.
• Knowledge of Microsoft Office and statistical analysis.
  
  
  

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.

Flexibility for U Program: Hybrid Model

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

Benefits Package

Contract of Employment: Temporary position

Location: Parets del Vallès.

www.grifols.com