?????? ???????????????????????????????? Deliver key improvements in Quality, Service, and Cost through structured engineering initiatives. Act as technical lead on product and process issues and drive root cause analysis. Drive process validation activities: IQ, OQ, PQ, VP, Gauge R&R, etc. Develop SOPs, work instructions, and documentation aligned to GMP. Lead cross-functional Continuous Improvement Programs (CIP). Transfer processes across facilities and support New Product Introduction (NPI). Provide engineering mentorship to technicians, operators, and engineers. Lead Value Stream and Cross-Functional Projects as assigned. Support audit readiness as a Subject Matter Expert (SME). Ensure strict adherence to EHS and Quality Management Systems (QMS). ???????????????? ???????????????????????????? Level 8 Degree in Mechanical Engineering or related field. 24 years of experience in a regulated manufacturing environment (preferably Med Tech). Proven Project Management capabilities. Hands-on experience in Process Validation and Problem Solving (Six Sigma). Strong documentation and communication skills. Autonomous, driven, and collaborative mindset. Excellent leadership, decision-making, and influencing abilities. Skills: Manufacturing engineering IQ OQ PQ VP GMP