Lead Engineer, Process Optimization

Lead Engineer, Process Optimization BioTissue Holdings Inc Miami, FL Job Details Full-time $124,500 - $155,000 a year 19 hours ago Qualifications Statistics Operational analysis Performance improvement leadership Program design Microsoft Outlook Production data analysis Defect resolution root cause analysis Requirements design Automation Workflow management (operations management method) ISO standards Spreadsheets Engineering Regulatory compliance Six Sigma methodology implementation Value stream mapping Engineering process optimization GMP Process mapping Key Performance Indicators Statistical analysis Analysis skills Bachelor's degree in engineering Industrial Engineering Requirements analysis Mentoring Project task coordination Industrial engineering Leading team collaboration initiatives Quality control problem-solving Full Job Description Position Summary The Senior Engineer, Process Optimization is a key technical leader responsible for developing and driving BioTissue's Continuous Improvement (CI) program. This expert-level role owns the creation and execution of the 12‑month CI pipeline—including Kaizens, 5S, statistical analysis, training, and other core CI methodologies—and plays a central role in shaping CI culture across the organization. Operating with significant autonomy, this position identifies improvement opportunities through both quantitative analysis and on‑the‑floor observation. The Senior Engineer partners closely with Operations, Engineering, Development, Production, Supply Chain, Distribution, Facilities, IT, and Quality to optimize manufacturing and operational processes, enhance product quality, and strengthen daily operational performance. This role is highly hands‑on and requires strong technical depth, cross‑functional collaboration, and the ability to lead change in a regulated GMP environment. Essential Duties & Responsibilities Process Optimization & Analysis Analyze existing workflows, equipment, and systems to identify bottlenecks, inefficiencies, and improvement opportunities. Conduct root cause analysis (RCA) to resolve production, quality, and operational issues. Identify opportunities to reduce scrap, waste, and raw material usage. Gather and translate business requirements into actionable improvement plans. Continuous Improvement Leadership Develop, manage, and execute the 12‑month Continuous Improvement Program plan. Lead CI initiatives using Lean, Six Sigma, and related methodologies (e.g., value stream mapping, 5S, Kaizen). Mentor teams in the application of CI principles, including early product development activities. Drive change management efforts to ensure adoption and sustainability of improvements. Cross‑Functional Support Partner with Operations leaders to develop and refine KPIs supporting inventory, productivity, quality, safety, and delivery goals. Support ERP/MES end‑users and contribute to system optimization efforts. Collaborate with Engineering, Manufacturing, Supply Chain, Distribution, Facilities, IT, and QA on cross‑functional improvement projects. Compliance & Quality Ensure all CI activities comply with BioTissue's Quality Management System and applicable regulatory requirements, including cGMP, FDA, ISO, and GTP standards. Skills & Abilities Technical Expertise Significant applied Continuous Improvement experience. Strong understanding of workflow optimization and process engineering. Experience with automation and AI‑assisted workflows. Proficiency with ERP and MES systems. Strong troubleshooting and analytical skills. Advanced proficiency in Microsoft Excel, Word, PowerPoint, and Outlook. Leadership & Behavioral Competencies Demonstrated ability to lead change, remove barriers, and promote CI culture. Strong communication and collaboration skills across diverse teams. Ability to coordinate multiple tasks with attention to detail and follow‑through. Tenacious, data‑driven, and proactive in identifying and addressing improvement needs. Regulatory & Quality Knowledge Thorough understanding of GTP, cGMP, quality systems, and compliance requirements. Position Expertise/Qualifications Bachelor's degree in engineering or similar required. Six Sigma black belt preferred 5 years process optimization/industrial engineering experience in a GMP manufacturing environment, preferred. Physical Requirements Sedentary work that generally requires sitting and/or standing