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.

We are looking for a Corporate Quality Specialist who will be part of the change and digital transformation, getting involved in the supervision of Grifols' quality systems through data analysis and the preparation of technical reports, as well as promoting and participating in projects for the harmonization and continuous improvement of quality systems.

What your responsibilities will be

• Review and update the corporate quality system:
  Draft and review quality system documents (policies, SOPs, reports, etc.).
  Implementation of electronic quality system.
• Supervise Grifols quality systems:
  Data analysis and reporting.
  Draft, review and approve technical reports.
  Study quality systems and compare them with current regulations.
  Review quality standards and monitoring their implementation at Grifols.
• Provide support in the management of global quality projects:
  Together with the manager, coordinate multidisciplinary teams to ensure that projects are carried out within the defined timing and with the expected quality.
  Draft, review and approve technical documentation.

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 Health Sciences or a related field.
• 3 years of pharma quality experience (Quality Systems, Quality Assurance, CVS and/or Audit).
• Experience collaborating in digital transformation projects and/or in software implementation.
• Advanced English Level.
• Excellent written and verbal communication skills.
• Good understanding of regulatory requirements and quality standards relevant to our products (biopharma, medical devices).
• Develop collaborative working relationships.
• Results-oriented and proactive mindset.
• Willingness to travel internationally as needed (maximum 30%).

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.

Benefits package

Contract of Employment: Permanent position

Location: Sant Cugat del Vallès

www.grifols.com

#LI-LS1

Location: SPAIN : España : Sant Cugat del Valles:SC3

Learn more about Grifols