Bachelor's degree in Engineering (Mechanical, Industrial, Electronics, Manufacturing, or a related field), Minimum 5 years of experience in Manufacturing or Process Engineering within a regulated medical device environment, including at least 3 years in a leadership position, Excellent command of English, both oral and written, Strong knowledge of medical device quality systems and regulations, including ISO 13485, EU MDR, FDA 21 CFR Part 820, ISO 14971, and MDSAP, Proven experience leading complex manufacturing investigations, CAPA activities, root cause analysis, and quality improvement initiatives, Hands-on experience with manufacturing risk management, PFMEA, process validation, and technology/design transfer projects, Strong analytical and statistical problem-solving skills; experience with Minitab or similar statistical software is preferred, Knowledge of manufacturing technologies such as injection molding, extrusion, automation, assembly, bonding, or sealing processes is an advantage, Lean Six Sigma Green Belt or Black Belt certification is preferred, Excellent leadership, communication, stakeholder management, and cross-functional collaboration skills, Willingness to travel domestically and internationally as required, Living in Antalya or willing to relocate. Within our Care Enablement segment, we develop and provide life-sustaining medical products, digital health solutions, and therapies that empower clinical teams and improve patient outcomes.