Assistant Manager- Assembly

Job Description

Job Description Mediplus India Ltd. is looking for a Assistant Manager -Assembly with deep experience in production and cleanroom operations. The ideal candidate should have over 10 years of experience in the medical device industry and be capable of leading shift-wise production execution, manpower handling, and maintaining regulatory compliance in cleanroom environments. Key Responsibilities Ensure preventive maintenance of machines as per defined schedules. Supervise and monitor cleanroom conditions and maintain all related records. Maintain and audit BMRs and cleanroom documentation. Assess and allocate manpower across direct and indirect production areas. Optimize machine and manpower utilization for maximum efficiency. Motivate and guide supervisors and workmen to ensure high team performance. Oversee entire production operations during shift and ensure execution of customer orders. Achieve daily production targets within the stipulated timeframe. Prepare work instructions and check sheets , and ensure proper documentation. Implement and monitor effective production planning in alignment with PPC requirements. Maintain control over inventory levels and raw material usage. Take corrective and preventive actions on in-process quality issues and customer complaints. Conduct on-the-job training for supervisor, junior staff, and workers. Handle administrative responsibilities for shift-level staff. Ensure smooth product movement from assembly to finished goods . Enforce strict adherence to SOPs, GMP, and ISO 13485 standards. Drive productivity improvement through lean ideas and process enhancements. Motivate workers and communicate shift-wise work goals and targets . Train operators on quality standards and safety protocols . Maintain production records, controlled documentation, rejection sheets, and traceability logs . Monitor rejection rates hourly , analyze trends, and implement improvements. Analyze and report low production reasons and machine breakdowns . Ensure batch-wise traceability and compliance throughout production. Provide accurate input in Material Management (M.M) data systems . Desired Candidate Profile Minimum 10 years of experience in a supervisory or shift incharge role in a medical device manufacturing environment . Strong knowledge of cleanroom operations, GMP, ISO 13485 , and PPC coordination . Proven ability to manage teams , maintain records, and ensure on-time delivery. Skilled in root cause analysis , production planning, and documentation. Is comfortable to work in shifts as the job involves shift rotation Key Skills Production Supervision, Clean Room Operations, GMP, Preventive Maintenance, BMR, ISO 13485, Rejection Analysis, Shift Management, Inventory Control, Team Leadership, Quality Compliance, PPC Coordination, Documentation, Medical Device Manufacturing