Key Responsibilities:

• Responsible for executing the production Plan & control Production processes effectively with Safety, Quality & Productivity in mind & aligning with PAN India initiatives related to stent market.
• Establish daily/weekly production meeting in terms of Production performance, production short fall, quality metrics, manufacturing bottlenecks and inventory execute to attain the same including generating consumption reports.
• Manpower planning & allocation of people on the manufacturing lines during the shifts. Identify manpower requirements and Coordinating with HR for manpower recruitment.
• Team management: Manage and lead a direct team and work closely with QA/RA team. Communicate production status to team and to upper management on a regular basis.
• Documentation control: To write the production process SOPs and to ensure that the training is been delivered to all user on time and file is updated with current revision.
• BMR (Batch Manufacturing Records): Batch record Sheets, production logbooks, other documents required to meet GMP & HSE requirements.
• Meeting the production targets & delivering the target OEE's. Prepare and execute plans to scale up production keeping in view the long-term business objectives of the company
• Maintain & perform Good Manufacturing Practices.
• Perform the SAP transactions for accounting of material & FG's.
• Production process audit: Determining quality control standards in consultation with marketing and QA/RA and adhering to the same.
• Coordinate raw & packing material planning with the warehouse.
• Support new products development, trials, validation & CIP projects.
• Control material wastage & meet the expected yields. Overseeing production processes/
• Implement/develop existing processes to minimize wastage and drive down overall      manufacturing costs Selecting, ordering, and purchasing materials in coordinating with stores and   purchasing.
• Organizing the repair and routine maintenance of production equipment to ensure calibration status is always maintained.
• Liaison with buyers, marketing/purchase, and sales staff to ensure required materials is available to support all aspects of the production.
• Introducing innovative manufacturing processes.

Experience: Minimum 10 Years of working experience within production and manufucturing environment of class III medical devices.