Senior Validation Lead

Senior Validation Lead – Pharmaceutical Manufacturing Location: Sweden Contract: Minimum 12-Month Fixed-Term Contract Potential: Opportunity to extend Employment Type: Full-Time Language: Swedish and English About the Assignment We are seeking an experienced Senior Validation Lead to join a major global pharmaceutical organisation and take responsibility for qualification and validation activities within a technology-intensive manufacturing and packaging environment. This is a key role supporting packaging operations, technical investments, equipment lifecycle management, automation and continuous improvement initiatives. You will ensure that equipment, processes and technical changes are appropriately qualified and validated in accordance with GMP requirements, regulatory expectations and internal quality standards. You will work closely with a broad range of stakeholders including Production, Engineering, Quality, Automation, Project Management and external suppliers. The environment is fast-paced and project-driven, with ongoing investment in manufacturing technology and packaging capabilities. The successful candidate will be comfortable taking ownership of validation activities from initial requirements definition through to approved implementation and will be able to translate regulatory and quality requirements into practical solutions for manufacturing operations. Key Responsibilities:

• Lead qualification and validation activities for pharmaceutical packaging lines, equipment and associated systems.
• Take ownership of validation activities across technical changes, investment projects, equipment modifications and continuous improvement initiatives.
• Ensure qualification and validation activities comply with GMP, GAMP 5, internal quality standards and applicable regulatory requirements.
• Prepare, review and approve validation documentation, including:
• User Requirements Specifications (URS)
• Risk Assessments
• IQ/OQ/PQ documentation
• Validation Plans and Protocols
• Validation Reports
• Supporting technical and quality documentation
• Support requirements definition and technical assessments relating to the procurement, installation, modification and lifecycle management of manufacturing and packaging equipment.
• Lead validation activities associated with serialisation, vision systems, labelling, track-and-trace and automated packaging solutions.
• Coordinate cross-functional validation teams and ensure activities rema