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Assistant Production Manager

Job in 600001, Chennai, Tamil Nadu, India
Listing for: Aurolab
Full Time position
Listed on 2026-09-19
Job specializations:
  • Manufacturing / Production
    Production QC/QA, Production Manager, Pharmaceutical Manufacturing, Quality Engineering
Job Description & How to Apply Below
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
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