5 goods and materials production jobs found in karnataka.

Understanding of Engineering Drawings.Understanding of GD&T (Geometric Dimensioning and Tolerancing). Knowledge of developing assembly and sub-assembly for automotive vehicle body and welding parts. Knowledge of automotive parts assemblies and sub-assemblies related to body and welding. Knowledge of PPAP documents like; PFD (Process Flow Diagram), FMEA (Failure Mode and Effects Analysis) and CP (Control Plan). Knowledge of JIG specifications and Design

● Strategic Process Transformation & Standardization○ Identify, standardize, and automate high-impact processes across GBS, ensuringalignment with enterprise goals and customer experience standards. Leverage bestpractices to create a cohesive, unified approach to operational excellence.● Portfolio Management & Prioritization○ Develop a portfolio of improvement projects that drive tangible cost savings,process efficiencies, and customer satisfaction.

As Production Supervisor, you will be accountable for shift-level execution and workforce supervision. 1. Shift & Line Execution•Execute daily production plans assigned by Production Management.•Ensure timely startup and closure of production lines.•Monitor batch progress and output targets. 2. Workforce Supervision & Discipline•Allocate operators and helpers to workstations.•Monitor attendance, punctuality, and conduct.•Provide on-the-job guidance and

Job Description :Check and confirm material availability for all WIP and planned projects.Conduct a meeting with production managers for previous day’s performance and update today’s production schedule.Review project wise Factory Orders (FOs) releases.Review project-wise material readiness and update shortage list.Coordinate with Buyers for prioritization of material procurement.Coordinate with key stakeholders - Design, Project Management, Procurement,

Required Attributes :Master’s degree/Ph.D in Biomedical Engineering, Life Sciences, Biotechnology, or a related field. 6-10 years of experience in regulatory affairs and quality management within the IVD or medical device industry. In-depth knowledge of global regulatory standards and quality management systems, including ISO 13485, ISO 14971, EU IVDR, US FDA 21 CFR 820, and CDSCO.Proven experience in leading regulatory submissions and successful product