Senior Validation Specialist

Quality Assurance Technician – Validations (Process and Cleaning Validation) Location: Greater Madrid area Sector: Pharmaceutical Manufacturing Type: Full-time, permanent About the Role We’re looking for an experienced Quality Assurance Technician to take a leading role in process and cleaning validation activities at a well-established pharmaceutical production site. This is a key quality role supporting both sterile and non-sterile product lines, offering strong long-term career potential. You’ll act as a technical reference within the Validation team, planning and executing validation protocols in compliance with GMP standards, working cross-functionally with Production, Quality Control, and Engineering teams, and supporting inspections and improvement initiatives across the site. Key Responsibilities Develop and execute Validation Master Plans for process and cleaning validation Prepare validation protocols, reports, and supporting documentation Ensure validation activities meet GMP standards and internal quality policies Work closely with Production, QC, and Projects teams to implement validation strategy Perform risk assessments, contribute to CAPAs and change controls Support site audits and inspections (internal, client, and regulatory) Contribute to quality system improvement and revalidation of ISO certifications What You’ll Need Degree in Pharmacy or Life Sciences 5 years of experience in pharmaceutical validation (ideally with sterile products) Strong understanding of GMP requirements Experience with systems like TrackWise, SAP, or similar QMS tools High level of English (spoken and written) Excellent attention to detail, technical writing skills, and ability to work cross-functionally Link to GxPeople Global Privacy Policy - https://www.gxpeople.com/cm/privacy

Location: Madrid, Community of Madrid, ES

Posted Date: 11/24/2025