Production Manager needed at Lorache Consulting Limited

Job Description

• 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

• 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.

Requirements

• 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.