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 _Quality Evaluation Specialist_ to join Quality department at Biomat SA, company dedicated to analyzing and controlling the plasma used by Instituto Grifols SA as raw material for the production of plasma derivatives. **What your responsibilities will be** + Coordinate the change control process for processes, facilities and equipment, both for Biomat S.A. and for change communications from suppliers. + Coordinate the deviation, complaints and CAPA management process, taking on the role of process manager who directs the workflows and coordinates the editing and execution of tasks in the computer system. + Update process indicators of Change Control, deviations, CAPA and complaints oriented towards continuous improvement. + Prepare documentation requested in audits carried out by national and international organizations and by other companies. **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 (Pharmacy, Biology, Chemistry), being valuable to have a Master or Postgraduate degree in the pharmaceutical sector. + You have 2 years of experience in similar position within pharma quality. + Knowledge in GMP. + You have knowledge in Basic Statistics. + You have knowledge of MS Office and SAP program. + You have advanced level of English. **** **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 **** **Flexible schedule:** Monday-Thursday 8h to 17h and Friday 8-15h. **** **Benefits package** **** **Contract of Employment:** Permanent position **Location:** Parets del Vallès www.grifols.com Learn more about Grifols (http://www.grifols.com/es/web/international/home) **Req ID:** 523389 **Type:** Indefinido tiempo completo **Job Category:** TECNICA