Descripción de la oferta
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, fostering an inclusive environment where diversity makes us outstanding. This position is for a Validation Specialist in the IVD (In Vitro Diagnostic) Systems Department within the Instruments Development & LCM (Life Cycle Management) Area at Diagnostic Grifols S.A. The role supports validation activities and complementary studies, ensuring compliance with applicable guidelines, procedures and regulations for IVD systems and the analytical laboratory. Responsibilities Perform IVD system validation activities, including planning, drafting, and supervision of protocol execution; collaborate in obtaining and analysing study data; contribute to the drafting of final validation reports for new products or product changes. Analyze deviations identified during validations and identify corrective and improvement actions related to IVD systems. Participate in cross‑functional/interdepartmental working meetings. Investigate root‑cause studies related to complaints concerning IVD systems. Analyse design requirements and specifications to identify and determine critical aspects related to user actions. Review IVD System Risk Analyses. Manage laboratory instrumentation, including relevant applications (databases, repositories) and monitor compliance with verification, calibration and qualification activities. Manage reagents and samples, including placing orders, stock control and expiration date monitoring. Ensure that laboratory instrumentation is used properly and responsibly. Qualifications Bachelor's degree in Health Sciences (Biotechnology, Biochemistry, Pharmacy, Biology, Chemistry Engineering, etc.) or equivalent (Diagnostic, Clinical Laboratory, etc.). Previous experience in a related field within the pharmaceutical sector is an advantage. Knowledge of statistical analysis. Proficiency with MS Office, especially Excel. Knowledge or experience with SAP or similar management software. Intermediate level of English. Ability to perform each essential duty satisfactorily; reasonable accommodations may be made for individuals with disabilities to perform the essential functions. Benefits Permanent employment contract. Opportunity for professional development in an excellent working environment. Schedule Afternoon shift. Location Parets del Vallès, Spain. Grifols is an equal opportunity employer. #J-18808-Ljbffr
