Review and validate engineering drawings for Manufacturability, Accuracy and Completeness as per the latest Engineering standards.
Apply knowledge of medical device regulations and execute gap assessments, manufacturing print reviews and remediation activities.
Participate in ideation activities to assess project scoping and viability through economic analysis, conflict analysis and supplier quote validation.
Experienced in product sustenance engineering activities with expertise across design, manufacturing, production processes and regulatory compliance. Skilled in coordinating with suppliers to resolve technical queries, ensuring timely and high-quality project delivery.
Conduct, review and update models for tol-stackup studies and dimensional variation analysis (1D/2D) using Creo-CETol OR other tools.
Apply project management skills to plan, schedule, and monitor project activities efficiently ensuring FTR & OTD excellence.
Qualification & Experience
Bachelor’s degree in mechanical/production engineering with Min 10–13 years of relevant experience.
Strong expertise in DFM&A principles and manufacturing methods for plastics, metals, and packaging components & Systems.
Proven experience in analyzing project feasibility for cost savings and efficiency improvements.
Proficiency in CAD - Creo/SolidWorks and PLM/PDM tools (preferably Windchill).