Laboratory Validation Assistant I+D

Description

Job Summary: We are seeking a Laboratory Validation Assistant to conduct tests, maintain instrumentation, and prepare reagents in an international healthcare setting. Key Highlights: 1. Join an international team improving global health. 2. Be part of a leading company in hemoderived medicines. 3. Professional development and continuous training in a positive environment. Would you like to join an international team working to improve the future of the healthcare sector? Do you want to contribute to improving the lives of millions of people? Grifols is a global healthcare company that has been enhancing people's health and well-being worldwide since 1909. We are leaders in hemoderived medicines and transfusion medicine, and we develop, manufacture, and market innovative medicines, solutions, and services in over 110 countries and regions. We believe diversity adds value to our business, our teams, and our culture. We are committed to equal opportunities and our mission is to provide an inclusive environment where differences strengthen our company. Join Diagnostic Grifols! Diagnostic Grifols SA is a company dedicated to the research, development, and manufacturing of high-technology products for in vitro clinical diagnostics. The IVD Systems Validation Department, located within the Instrument Development \& LCM area of Diagnostic Grifols S.A., seeks to hire a *Laboratory Validation Assistant.* **Your responsibilities will include:** * Conducting tests described in validation or verification protocols for systems (instruments and associated reagents) and documenting obtained data to demonstrate compliance with established acceptance criteria. * Maintaining instrumentation used, performing defined maintenance and calibration operations. * Preparing and handling reagents and/or materials required for conducting tests, including inventory monitoring, identification, and proper storage. * Performing calculations related to measurements using equipment or computer software when necessary. * Ensuring documentation remains current at all times. * Applying existing Quality, Safety, and Health standards applicable in your area. * Drafting analysis reports or related records to communicate obtained results, as well as ensuring proper preservation and archiving of such documents. * Monitoring trends in controls performed across different analyses to support continuous improvement. * Conducting verification and calibration tests on instruments and standards. * Executing validation or verification protocols for instruments and associated reagents, and documenting obtained data to demonstrate compliance with established acceptance criteria. **Who You Are** * You hold a Higher Vocational Training Degree in Clinical and Biomedical Laboratory. * You have knowledge of Microsoft Office suite. * Intermediate English proficiency is valued. * Experience in a clinical laboratory is valued. * Experience in the functions described is valued. **What We Offer** * Working hours: Afternoon shift * Employment contract: Temporary Being part of Grifols means the opportunity to work in an internationally oriented environment that promotes equal opportunities. It means the opportunity to develop professionally, benefit from continuous training, and integrate into a team of professionals where each individual contribution matters. Our commitment is to maintain an environment that supports the professional development of our employees in a positive workplace. Human capital is key both to carrying out Grifols' activities and to the company's expansion process. If you are interested in growing with us and your profile matches this professional opportunity, please send us your CV. **Location:** **SPAIN : Spain : Parets del Valles****:****\[\[cust\_building]]** Learn more about Grifols