PurposeTo execute validation activities in compliance with regulatory requirements and company standards. The Validation Engineer supports the Validation Team Lead in implementing the Validation Master Plan, maintaining validation-related SOPs, and performing validation for processes, cleaning, equipment, analytical instruments, and utilitieResponsibilitiesDevelop, execute, and document validation protocols and reports for process, cleaning, equipment, analytical instruments, and utilities.Ensure validation activities comply with GMP, regulatory guidelines, and internal procedures.Support technology transfers and new product introductions through validation activities.Maintain accurate and complete validation documentation in accordance with SOPs and regulatory requirements.Assist in updating and implementing validation-related SOPs under the guidance of the Validation Team Lead.Ensure validation records are audit-ready and support internal and external inspections.Identify opportunities to improve validation processes and enhance efficiency.Contribute to initiatives that align validation practices with evolving regulatory expectations.Work closely with manufacturing, quality, engineering, and analytical teams to coordinate validation activities.Provide technical support during troubleshooting and investigations related to validation.RequirementsDegree in Engineering, Pharmaceutical Science, or related discipline.2-4 years in validation within a GMP-regulated environment.Experience in process, cleaning, and equipment validation preferred.Strong understanding of GMP and validation principles.Excellent documentation and organizational skills.Ability to work collaboratively across functions.Solid knowledge of validation methodologies and regulatory requirements.Ensures accuracy and completeness in validation documentation.Ability to troubleshoot and resolve validation-related issues.Works effectively with cross-functional teams.Commitment to maintaining high standards of quality and regulatory compliance.