Assistant Manager - Production

5 - 8 years

6 - 8 Lacs

Posted:1 day ago| Platform: GlassDoor logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Complete Production Responsibility

Position Overview

We are seeking a dynamic and experienced Assistant Manager - Production at the level of Shift Incharge with complete responsibility for production operations. This critical role requires hands-on leadership in pharmaceutical manufacturing, ensuring optimal production efficiency, quality compliance, and team performance. The successful candidate will be responsible for end-to-end production management, from raw material utilization to finished product dispatch.

Location: India
Employment Type: Full-time, Permanent
Reporting To: Production Manager
Team Size: 15-25 people production team

Key Responsibilities

Production Operations Management

  • Take full ownership of all production activities
  • Ensure seamless production flow from raw material receipt to finished goods
  • Monitor and optimize production schedules to meet daily/weekly targets
  • Coordinate with all shifts for smooth handover and continuity
  • Manage production line changeovers and setup activities efficiently

Manufacturing Excellence

  • Oversee pharmaceutical manufacturing processes including dispensing, mixing, granulation, compression, coating, and packaging
  • Ensure optimal equipment utilization and minimize downtime
  • Monitor critical process parameters and maintain process control
  • Implement continuous improvement initiatives to enhance productivity
  • Manage production scheduling and resource allocation effectively

Batch Management

  • Review and approve batch manufacturing records (BMR)
  • Ensure accurate batch documentation and record maintenance
  • Monitor in-process controls and sampling procedures
  • Coordinate with QC for timely release of batches
  • Manage batch reconciliation and yield optimization

Quality Assurance & Compliance

  • cGMP Compliance
  • Ensure strict adherence to current Good Manufacturing Practices (cGMP)
  • Maintain cleanroom protocols and environmental monitoring
  • Implement and monitor Standard Operating Procedures (SOPs)
  • Conduct regular compliance audits and corrective actions
  • Ensure proper documentation and record-keeping practices
  • Quality Management
  • Monitor product quality parameters and specifications
  • Coordinate with Quality Control and Quality Assurance departments
  • Implement corrective and preventive actions (CAPA) as required
  • Ensure proper handling and storage of raw materials and finished products
  • Maintain traceability and batch genealogy records
  • Regulatory Compliance
  • Ensure compliance with Drug Controller General of India (DCGI) regulations
  • Maintain EU-GMP, WHO-GMP, and other international standards as applicable
  • Support regulatory inspections and audits
  • Implement regulatory updates and changes in manufacturing practices

Team Leadership & Management

  • People Management
  • Lead and motivate a team of production operators, technicians, and support staff
  • Conduct shift briefings and communicate daily objectives and priorities
  • Provide on-the-job training and skill development for team members
  • Manage attendance, performance, and disciplinary actions as required
  • Foster a positive work environment promoting teamwork and collaboration
  • Performance Management
  • Set clear performance expectations and KPIs for team members
  • Conduct regular performance reviews and provide constructive feedback
  • Recognize and reward outstanding performance
  • Address performance issues and implement improvement plans
  • Support career development and succession planning

Safety & Environment Management

  • Occupational Health & Safety
  • Ensure compliance with all safety protocols and procedures
  • Conduct safety briefings and promote safety awareness
  • Investigate accidents and incidents, implement corrective measures
  • Maintain safety equipment and emergency response procedures
  • Achieve zero-accident targets and promote safety culture
  • Environmental Compliance
  • Monitor environmental parameters and waste management
  • Ensure proper disposal of pharmaceutical waste
  • Implement environmental sustainability initiatives
  • Maintain compliance with pollution control board requirements
  • Monitor water and energy consumption optimization

Equipment & Maintenance Management

  • Equipment Operations
  • Ensure proper operation and maintenance of manufacturing equipment
  • Coordinate with maintenance team for preventive and corrective maintenance
  • Monitor equipment performance and identify improvement opportunities
  • Maintain equipment logs and performance records
  • Maintenance Coordination
  • Schedule and coordinate maintenance activities with minimal production impact
  • Ensure availability of critical spare parts and consumables
  • Monitor equipment efficiency and OEE (Overall Equipment Effectiveness)
  • Support equipment qualification and validation activities
  • Implement predictive maintenance strategies

Planning & Coordination

  • Production Planning
  • Participate in daily production planning meetings
  • Coordinate with Planning department for material requirements
  • Monitor inventory levels and ensure material availability
  • Optimize production sequences and batch sizes
  • Manage production priorities and urgent requirements
  • Cross-functional Coordination
  • Coordinate with Quality Control for sampling and testing
  • Liaise with Warehouse for material receipt and dispatch
  • Work with Engineering for technical support and improvements
  • Collaborate with other shifts for seamless operations
  • Support Supply Chain for delivery commitments

Required Qualifications

Educational Background

  • Essential: Bachelor's degree in Pharmaceutical Sciences, Other Science Streams, Chemical Engineering, or related field
  • Preferred: Master's degree in Pharmaceutical Technology, Industrial Pharmacy, or MBA

Experience Requirements

  • Minimum Experience: 5-8 years in pharmaceutical manufacturing operations
  • Leadership Experience: At least 2-3 years in supervisory or team leadership roles
  • Industry Experience: Solid oral dosage form or injectable manufacturing experience
  • Shift Management: Previous experience in shift operations and 24/7 manufacturing environment
  • Regulatory Experience: Exposure to regulatory inspections and compliance requirements

Technical Competencies

  • Manufacturing Processes: Deep understanding of pharmaceutical manufacturing processes and equipment
  • Quality Systems: Thorough knowledge of cGMP, ISO standards, and quality management systems
  • Equipment Knowledge: Familiarity with tablet compression, coating, packaging, and related equipment
  • Documentation: Proficiency in batch record review, deviation handling, and GMP documentation
  • Problem Solving: Strong analytical and troubleshooting skills for production issues

Leadership & Management Skills

  • Team Leadership: Proven ability to lead and motivate production teams
  • Communication: Excellent verbal and written communication skills in English and Hindi
  • Decision Making: Ability to make quick decisions under pressure
  • Conflict Resolution: Skills in handling team conflicts and personnel issues
  • Training: Experience in conducting training and development programs

Job Types: Full-time, Permanent, Fresher

Pay: ₹50,000.00 - ₹70,000.00 per month

Benefits:

  • Commuter assistance

Education:

  • Bachelor's (Required)

Experience:

  • pharmaceutical production: 2 years (Required)
  • Production management: 2 years (Preferred)

Work Location: In person

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