Overview We are seeking a highly skilled and experienced Software Validation Engineer (MES) to join our dynamic team. The ideal candidate will possess a strong blend of technical expertise and soft skills, ensuring the reliability and quality of our software products. Responsibilities Lead and execute software validation activities, ensuring compliance with CSV-SDLC standards. Develop and maintain professional documentation, including validation plans, protocols, and reports. Perform validation tasks using JIRA, tracking progress and resolving issues efficiently. QA & PD IRIS change control Traceability Matrix (TM) UAT (User Acceptance Test) Matrix Design Specification documentation Creation and completion of CP, CSCA, Test Protocols, and Test Reports Provide expertise in ThinManager (preferred) to enhance validation processes Support and validate MES (Manufacturing Execution Systems), preferably within medical device environments, ensuring alignment with regulatory and quality standards Communicate effectively in advanced English, both written and verbal, to articulate technical concepts and collaborate with global teams Basic Qualifications Bachelor's degree in Computer Science, Engineering, or a related field Minimum of 3 years of experience in software validation or a related role Experience working with MES platforms in medical devices or similarly regulated industries is highly desirable Strong analytical and problem-solving skills Excellent communication and interpersonal skills Knowledge of ThinManager (preferred) Advanced proficiency in English Seniority level Not Applicable Employment type Contract Job function Consulting, Engineering, and Manufacturing Industries Medical Equipment Manufacturing, Manufacturing, and Business Consulting and Services Note: This description reflects the responsibilities and qualifications for the Software Validation Engineer role and is intended for applicants in relevant regulated environments. J-18808-Ljbffr