Work Flexibility: Hybrid

What you will do:

• Work closely with manufacturing locations in development & review of manufacturing process for new products / line extensions.
• Prepare Process Failure Mode & Effect Analysis (pFMEA) & Control Plans for new products / line extensions.
• Prepare inspection plans and guide sheets.
• Prepare, document, and facilitate qualification/validation of equipment, inspection methods, and manufacturing/assembly processes.
• Prepare/develop manufacturing assembly procedures and digital work instructions for complex electromechanical assemblies and tests
• Provide estimates of effort in an agile sprint-based project management setting on upcoming workload and identify cross-functional dependencies and blockers.  

What You will need: 

• Candidate should have Project Management experience in managing manufacturing process development for New Product.
• Proficient in preparing Process Flow Maps, Work Instructions/Standard Operating Procedures, pFMEA, and Process Control Plans
• Good knowledge of manufacturing process (preferable experience: assembly, torque applications, ESD-control, MES systems, Poka-Yoke techniques, test development for finished assemblies)
• Good knowledge of inspection methods of machined product
• Proficient in interpretation of drawing with GD&T
• Good Knowledge of Statistical Process Control techniques & Measurement System Analysis
• Knowledge of IQ, OQ, and PQ for equipment and processes in a medical device regulated industry
• Technical Writing

• Experience: 5~7 years in an engineering role.

• Education- B.E / B.Tech. - Mechanical Engineer

Preferred Skill Sets:

• Working knowledge of Valgenesis digital validation software
• Working knowledge of OnePLM for document change management

Travel Percentage: 20%