BEPC is actively looking for an Automation Engineer in San Angelo, TX area!3+ years of experience in automation engineering within a regulated industry (preferably medical devices or pharmaceuticals).1 Year contract with possible extensions!Benefits include medical, dental, vision, and life insurance We are seeking a detail-oriented and innovative Automation Engineer to support the design, development, implementation, and optimization of automated manufacturing and test systems for medical device production. The ideal candidate will work closely with cross-functional teams to improve operational efficiency, ensure regulatory compliance, and maintain the highest quality standards in a highly regulated environment. Summary of Duties and Responsibilities:Design, develop, and implement automated equipment and control systems (PLC, HMI, SCADA) to support manufacturing and quality processes.Lead automation projects from concept through validation, including equipment selection, integration, and commissioning.Collaborate with Manufacturing, Quality, R&D, and Regulatory teams to ensure automation systems meet technical, safety, and compliance requirements (FDA, ISO 13485, GMP).Author and execute validation protocols (IQ, OQ, PQ) for new or modified equipment and processes by internal procedures and industry regulations.Perform root cause analysis and implement corrective and preventive actions (CAPA) for process deviations or equipment failures.Support continuous improvement initiatives by identifying opportunities to automate manual operations or enhance existing automation systems.Manage system documentation, including design specifications, user requirements (URS), functional specifications (FS), and software lifecycle documents (SDS, FAT, SAT).Train maintenance and operations staff on new automation systems, troubleshooting techniques, and safety procedures.Maintain compliance with site policies, procedures, and safety regulations, including EHS guidelines.Participate in risk assessments (FMEA, Hazard Analysis) to identify and mitigate potential failure modes in automated systems.Perform other duties as required.Qualifications: Bachelor’s degree in Electrical Engineering, Mechatronics, Automation, Biomedical Engineering, or a related field.3+ years of experience in automation engineering within a regulated industry (preferably medical devices or pharmaceuticals).Hands-on experience with PLC programming (Allen-Bradley, Siemens, etc.), robotics, vision systems, and HMI/SCADA interfaces.Strong knowledge of equipment validation (IQ/OQ/PQ), GAMP5, and FDA 21 CFR Part 11.Familiarity with ISO 13485, ISO 14971, and Good Manufacturing Practices (GMP).Proficient in technical documentation, troubleshooting, and data analysis tools (e.g., Minitab, Excel).Excellent project management and cross-functional collaboration skills.Effective verbal and written communication.Preferred Qualifications: Experience in cleanroom or aseptic manufacturing environments.Six Sigma Green Belt or Black Belt certification.Experience with MES, SCADA, or ERP integration.