Assistant Production Manager

Aurolab; Madurai District; On-site; INR 600,000 - 900,000; Full time

Job summary

Aurolab in Tamil Nadu (Madurai district) seeks an experienced production professional with B.Pharm to manage batch production, ensure GMP/compliance, and maintain batch records.

You will coordinate with QA, R&D and production teams, implement SOPs, perform validations, audits, and ensure uninterrupted material availability for continuous manufacturing.

Qualifications

• Bachelor of Pharmacy is required.
• 5–8 years of experience in pharmaceutical manufacturing.
• Experience with batch records, SOPs, and GMP compliance.

Responsibilities

• Plan and execute batch production based on marketing requirements and production plans.
• Weigh ingredients and prepare batches per approved procedures.
• Monitor production processes and ensure compliance with CE/ISO/WHO-GMP standards.
• Establish, review, and implement SOPs related to manufacturing and maintenance.
• Participate in validations and ensure proper completion of BPRs.

Skills

Batch production

Documentation

SOPs

GMP compliance

Quality audits

Education

B.Pharm

Job description

Key Responsibilities:

• Plan and execute batch production based on marketing requirements and production plans.


• Perform weighing of ingredients/raw materials according to batch size and prepare batches as per approved procedures.


• Monitor overall production processes. Sanitization of packing materials and production equipment, Clean room operations and environmental conditions, Filtration and filling processes, Steam and dry heat sterilization, In-process and final product checks, Packing, finished goods storage, and shipment activities.


• Establish, review, and implement Standard Operating Procedures (SOPs) related to manufacturing, maintenance, and production processes.


• Participate in and document validation activities, including clean room, sterilizer, packaging, and other production-related validations.


• Ensure accurate completion, verification, and approval of Batch Production Records (BPRs) for each batch.


• Conduct internal quality audits for other divisions as per the audit schedule and participate as an auditee during internal and external audits.


• Ensure products are manufactured and maintained in compliance with applicable CE, ISO, and WHO-GMP requirements.


• Maintain effective document and data control for production and quality-related activities.


• Coordinate with the QA Manager to implement corrective and preventive actions related to production, quality, and customer requirements.


• Ensure adequate availability of raw materials, packing materials, consumables, and accessories required for uninterrupted production.


• Coordinate with R&D and Quality Assurance for new product introduction, product development, and improvement of production processes.


• Provide training to production staff on manufacturing procedures, GMP requirements, SOPs, and other production-related activities.


• Perform Equipment Performance Qualification (PQ) and prepare validation protocols in compliance with GMP and applicable regulatory requirements.


• Monitor production activities to ensure compliance with approved procedures, quality standards, and production schedules.


• Support continuous improvement initiatives to enhance productivity, process efficiency, product quality, and regulatory compliance.

Educational qualification: B.Pharm

Experience: 5 - 8 Years