Quality Evaluation Specialist

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.

<span 72="">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.

<span 72="">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

• <span 72="">Coordinate the change control process for processes, facilities and equipment, both for Biomat S.A. and for change communications from suppliers.
• <span 72="">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.
• <span 72="">Update process indicators of Change Control, deviations, CAPA and complaints oriented towards continuous improvement.
• <span 72="">Prepare documentation requested in audits carried out by national and international organizations and by other companies.

Who you are

<span 72="">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<span 72="">)<span 72="">.

• <span 72="">Bachelor's degree in Health Sciences (Pharmacy, Biology, Chemistry), being valuable to have a Master or Postgraduate degree in the pharmaceutical sector.
• <span 72="">You have 2 years of experience in similar position within pharma quality.
• <span 72="">Knowledge in GMP.
• <span 72="">You have knowledge in Basic Statistics.
• <span 72="">You have knowledge of MS Office and SAP program.
• <span 72="">You have advanced level of English.

<span 72="">What we offer

<span 72="">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. 

<span 72="">Information about Grifols is available at <span 72="">www.grifols.com.<span 72=""> 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! 

<span 72="">We look forward to receiving your application! 

<span 72="">Grifols is an equal opportunity employer. 

<span 72="">Flexibility for U Program: <span 72="">Hybrid

<span 72="">Flexible schedule: <span 72="">Monday-Thursday 8h to 17h and Friday 8-15h.

<span 72="">Benefits package

<span 72="">Contract of Employment:<span 72=""> Permanent position

Location: <span 72="">Parets del Vallès

<span 72="">www.grifols.com

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

Learn more about Grifols