Assistant Manager- Assembly

Assistant Manager -Assembly

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