Validation Technician

Description

Job Summary: We are seeking a Validation Technician to manage and execute equipment and process validation projects within a global healthcare company. Key Highlights: 1. Work in an internationally oriented environment 2. Opportunity for professional development and continuous training 3. Integration into a team of professionals where every contribution matters 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 plasma-derived 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.** Within the Validation Department at Instituto Grifols, we require a *Validation Technician* for equipment and processes, whose primary mission will be to manage and execute assigned validation projects in accordance with applicable regulations, ensuring the validity of manufacturing processes. **Your responsibilities will include:** * Drafting, reviewing, and approving qualification protocols and reports. * Drafting, reviewing, and approving validation protocols and reports. * Executing qualification and validation studies. * Updating validation protocols to reflect current regulatory requirements. * Documenting deviations, tracking CAPAs, and assessing change controls. **Who You Are** To perform this role successfully, a candidate must be capable of fulfilling the responsibilities satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the position. * Bachelor’s degree in Technical or Industrial Engineering, or a Bachelor’s degree in Health Sciences; a Master’s degree in the Pharmaceutical Industry is desirable. * 1–3 years of experience in a similar position. * Advanced level of English (minimum B2.2). * Proficiency in Microsoft Office and basic user-level knowledge of SAP. * Willingness and availability for occasional travel. **What We Offer** Joining Grifols means the opportunity to work in an internationally oriented environment that promotes equal opportunities. It means the opportunity to develop professionally, access continuous training, and integrate into a team of professionals where each individual’s contribution counts. Our commitment is to maintain an environment that fosters the professional development of our employees within a positive workplace atmosphere. Grifols’ human capital is key both to carrying out daily activities and to the company’s expansion process. We believe in diverse talent and aim to eliminate any barrier that might hinder your participation. If you require any accommodation during our selection process, please do not hesitate to inform us when applying. We are here to support you. If you are interested in growing with us and your profile matches this professional opportunity, please send us your CV. **Flexible schedule:** Monday–Thursday: 7–10 a.m. and 4–7 p.m.; Friday: 8 a.m.–3 p.m. **Employment contract:** Permanent **Benefits package** **Flexibility for U Program:** 1 remote working day per week **Location: Parets del Vallès.** #LI-AC3