Production Manager at Lorache Consulting Limited

The Production Manager will ensure the delivery of goods and services that meet our stringent quality standards, in the right quantities, and at the right times, all while minimizing costs. This ideal candidate will play a pivotal role in optimizing our production processes and improving efficiency across the board.

Responsibilities:

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• Oversee the smooth functioning of day-to-day operations within the production unit.
  
• Accountable for achieving quality production standards and meeting production targets.
  
• Plan and control inventory of raw materials and packing materials.
  
• Develop daily, weekly, and monthly material requirements based on production plans.
  
• Create and implement production plans in coordination with logistics, planning, and procurement.
  
• Lead new product development initiatives.
  
• Monitor dispatches of finished goods as per marketing requirements.
  
• Prepare MRM (Material Requirement Matrix) and QRM (Quality Requirement Matrix).
  
• Verify Batch Manufacturing Record (BMR) and Batch Packing Record (BPR) upon completion of each batch
  
• Ensure timely completion of production documentation, including batch records,
  
• SOPs (Standard Operating Procedures), and compliance records, maintaining accuracy and completeness.
  
• Collaborate with various service departments such as Engineering, QCQA, HR/Admin, Logistics, Planning, and Procurement.
  

Required Skills / Experience:

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• Min. B. Pharm.
  
• Minimum of 10 years of experience working in pharmaceutical manufacturing with at least 5 years of experience in a managerial role
  
• Good knowledge of local language & Excellent communication skills
  
• Strong analytical and excellent presentation skills
  
• Minimum of 10 years of experience in pharmaceutical manufacturing of Syrups, Capsules, Tablets and Infusions, with at least 5 years in a supervisory or managerial role.
  
• Thorough understanding of cGMP regulations, pharmaceutical manufacturing processes, quality systems.
  
• Sound knowledge of regulatory requirements and must be conversant with WHO GMP standards.
  
• Willingness to work in shifts as needed to support production operations.