VALIDATION ENGINEER

ALTEN Spain, a leading force in the IT, Engineering and Life Sciences industries. We are currently seeking a dedicated and detail-oriented Validation Engineer to involve in a 100% full remote position.ALTEN GroupWithin 30 years, ALTEN has become leader in both outsourced Engineering and IT Enterprise Services. ALTEN, composed of 54,000 employees (88% engineers), carries out complex and highly technical projects throughout the value chain of 6,500 clients, the most prestigious companies in all sectors of industry, services and telecommunications. We work with key actors in the Aeronautics & Space, Defense & Naval, Security, Automotive, Rail, Energy, Life Sciences, Finance, Retail, Telecommunications and Services sectors.Do you want to work in exciting projects at renowned clients? At ALTEN we believe that knowing and meeting the expectations of our consultants is a key factor in our success. Our consultants make the difference. Do you want to make the difference too?As a Validation Engineer, you will responsible for planning, executing, and documenting tests to ensure that products and systems meet established quality requirements, regulations, and standards, ensuring their safe and efficient operation.Responsibilities:Develop, execute, and document validation protocols (IQ, OQ, PQ) for equipment, systems, and processes, ensuring compliance with regulatory requirements.Collaborate in planning and managing validation projects, working with other departments to define and optimize processes.Perform risk analysis and assess validation process changes when necessary.Ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulations (FDA, EMA, etc.).Review and maintain validation documentation, including procedures, reports, and action plans.Support internal and external audits by providing necessary documentation and information to demonstrate compliance of systems and processes.Requirements:Bachelor’s degree in Engineering, Quality Sciences, Pharmaceutical Sciences, or related fields.Minimum of 6 years of experience in validation of processes, equipment, and/or systems in regulated industries (pharmaceutical, biotechnology, or similar).Knowledge of industry regulations such as GMP, FDA, EMA, and validation guidelines.Strong data analysis and problem-solving skills, with a collaborative team-oriented approach.Excellent verbal and written communication skills to work effectively with multidisciplinary teams.Minimum English level C1.Why Join Us?Possibility to work with cutting-edge technology in the Life Sciences industry.Collaborative and dynamic work environment.Possibility to join a top-leading company in the industry.Continuous trainings.Possibility to join different and interesting projects.If you want to embrace in a new and challenging opportunity and are excited about the opportunity to contribute to our team, we want to hear from you!