ppWould 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 integral 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. /p pbWe 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. /b /p h3Mission /h3 pThe IT Validation Technician actively contributes to the execution of the defined validation methodologies which comply with company standards and regulatory requirements. This role also oversees teams and validation resources engaged in validation activities. /p h3What your responsibilities will be /h3 ul liRelationship Management, Planning, and Strategic Alignment ul liBuilds effective and trusting working relationships with all business and IT partners in areas of responsibility and collaboration. /li liContinuously improves knowledge of business processes, industry trends, and IT systems to better communicate IT capabilities and support IT solutions development. /li /ul /li liProject Delivery and Management ul liProactively identifies project risks and issues, helps determine necessary escalation, mitigation, and resolution steps. /li liRegularly communicates deliverables status, concerns, and issues to direct Manager, the Project Manager, and the project team. /li liParticipates in estimating project cost and time requirements,



assessing capabilities and support/resource requirements in area of responsibility. /li liCreates, reviews, updates, and may approve CSV documentation for changes and projects as assigned in accordance with IT Methodology: Validation Plans, Risk Analysis, Validation Test Designs and Reports. /li liAssures the compliance of the GxP relevant IT systems with the regulatory and data integrity requirements. /li /ul /li liIT Operational Support ul liEnsures IT quality and regulatory compliance through adherence to quality control standards in all activities. /li liContributes to the development, documentation, and evolution of IT policies, procedures, and tools to align with business and IT strategies and ensure sustainability of services /li liRegularly communicates individual task status, open issues, and challenges to impacted stakeholders and/or direct manager. /li /ul /li liKnowledge Sharing and Consulting ul liParticipates in the education of partners in industry and IT best practices in areas of responsibility and expertise. /li liMentors peers and junior level staff with both challenging and routine assignments by sharing knowledge and experience. /li liShares developing expertise of industry and IT best practices with peers and business partners. /li liMay participate in the development of ongoing training for IT staff in specific areas of knowledge.



/li liProvides support in the event of internal and external audits of validated systems, preparing supporting documentation as required. /li /ul /li liParticipates in the continuous enhancement of systems, technologies, methodologies, and services to improve IT effectiveness and system performance. /li /ul h3Who you are /h3 pTo 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 accommodation may be made to enable individuals with disabilities to perform the essential functions. /p ul liBachelor’s degree in Life Sciences (Biology, Pharmacy, Biotechnology, Chemical or a related discipline). /li liMinimum of 3 years of proven experience working within a regulated pharmaceutical environment, including GxP compliance. /li liSolid understanding of project management methodologies, tools, and best practices. /li liKnowledge of regulatory requirements and GxP standards applicable to computerized systems. /li liExperience supporting regulatory inspections and audit responses. /li liStrong attention to detail with the ability to manage multiple priorities simultaneously. /li liAbility to work both independently and collaboratively in cross‑functional and international teams. /li liExcellent organizational, communication, and problem‑solving skills. /li liAdvanced in English, with the ability to work effectively in an international environment. /li /ul h3Benefits package /h3 ul liFlexibility for U Program: Hybrid Model. /li liContract of Employment: Permanent position. /li /ul pGrifols is an equal opportunity employer. /p /p #J-18808-Ljbffr

📌 Validation Technician (Parets)
🏢 Grifols
📍 Parets