Bepc inc. provides specialized engineering solutions and it project management services to fortune 500 companies in the life science and technology industries. Bepc mexico, a division of bepc incorporated, provides and manages consulting services for automotive and medical device companies throughout mexico and around the globe. We are seeking avalidation engineer iii (sdlc)to support validation activities in a regulated medical device environment. This role will focus on software development life cycle (sdlc) validation, ensuring that software systems, processes, and technologies meet regulatory, quality, and internal compliance standards throughout the entire lifecycle. The senior validation engineer will be responsible for developing and executing computer software validation (csv) documentation, supporting validation activities in systems such as mes, and collaborating with cross-functional teams including engineering, it, quality, and cybersecurity. The position plays a key role in ensuring that validation deliverables meet established standards and project requirements.key responsibilities: develop, review, and execute computer software validation (csv) documentation aligned with sdlc principles. Ensure validation activities comply with software development life cycle (sdlc) requirements and regulatory standards. Support validation activities for software systems integrated with mes environments. Perform and document user acceptance testing (uat) and validation test protocols. Conduct and document computer system change assessments (csca). Generate and maintain validation and asset management documentation according to project and quality requirements. Execute validation workflows and documentation tracking using jira. Collaborate with engineering, it, ot, quality, and cybersecurity teams to support validation deliverables. Provide project updates and escalate risks or issues to project leadership when necessary. Ensure validation deliverables meet internal quality standards and regulatory expectations.main qualifications: bachelor's degree in engineering, computer science, or a related technical field. 4+ years of experience in the medical device industry. Proven experience in software development life cycle (sdlc) validation. Strong experience in computer software validation (csv) in regulated environments. Experience working with mes systems. Hands-on experience with user acceptance testing (uat) and validation documentation. Experience performing computer system change assessments (csca). Experience using jira for validation documentation and workflow management. Intermediate english proficiency (written and conversational). Availability to work flexible hours.