Manager - Production
Piramal Pharma Limited
All India • 2 months ago
Experience: 5 to 9 Yrs
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Job Description
Role Overview:
As a Manager - Production, your primary responsibility will be to oversee various production activities and ensure adherence to quality, health, and safety standards. You will be required to manage a wide range of tasks related to batch manufacturing, quality management, compliance, and departmental coordination. Your role will involve maintaining cleanliness, implementing QEHS policies, determining internal and external issues, ensuring worker participation, and continuous improvement projects. Additionally, you will be responsible for productivity optimization, quality assurance, data integrity, and sanitation activities.
Key Responsibilities:
- Review batch manufacturing records
- Prepare QMS documents and upload them in the TrackWise system
- Handle change control, SOP, incident, deviation, and CAPA in TrackWise
- Maintain department cleanliness
- Implement QEHS policy & objectives
- Ensure worker participation and consultation
- Identify and communicate incidents, QEHS nonconformities, and take corrective actions
- Ensure work permit system during maintenance activities
- Implement QEHS continual improvement projects and monitor progress
- Prepare and review departmental SOPs and documents
- Coordinate, monitor, and control departmental activities as per cGMP norms
- Verify raw materials and packing materials
- Monitor dispensing, granulation, compression, and coating activities
- Update departmental documents and records
- Train operators and workers, and maintain training records
- Maintain inventory of machine accessories and change parts
- Provide requisition & review of BMRs and BPRs to the QA department
- Update KPIs and investigate root cause analysis of identified problems
- Report near miss incidents to Human Resources and safety department
- Plan manpower requirements under the guidance of HOD
- Utilize resources effectively for higher productivity
- Ensure product quality, cleanliness, and compliance with safety measures
- Complete monthly production plan and verify weighing balances
- Coordinate external parties for calibration of instruments
- Prepare documents for ISO 9001:2015, 14001:2015 & 18001:2007 compliance
- Ensure effective sanitation & hygiene activities at all levels
- Report hazards, incidents, accidents, and near misses
Qualifications Required:
- Bachelor of Pharmacy (B.Pharm)
- Full-time availability
(Note: No additional details about the company were provided in the job description.) Role Overview:
As a Manager - Production, your primary responsibility will be to oversee various production activities and ensure adherence to quality, health, and safety standards. You will be required to manage a wide range of tasks related to batch manufacturing, quality management, compliance, and departmental coordination. Your role will involve maintaining cleanliness, implementing QEHS policies, determining internal and external issues, ensuring worker participation, and continuous improvement projects. Additionally, you will be responsible for productivity optimization, quality assurance, data integrity, and sanitation activities.
Key Responsibilities:
- Review batch manufacturing records
- Prepare QMS documents and upload them in the TrackWise system
- Handle change control, SOP, incident, deviation, and CAPA in TrackWise
- Maintain department cleanliness
- Implement QEHS policy & objectives
- Ensure worker participation and consultation
- Identify and communicate incidents, QEHS nonconformities, and take corrective actions
- Ensure work permit system during maintenance activities
- Implement QEHS continual improvement projects and monitor progress
- Prepare and review departmental SOPs and documents
- Coordinate, monitor, and control departmental activities as per cGMP norms
- Verify raw materials and packing materials
- Monitor dispensing, granulation, compression, and coating activities
- Update departmental documents and records
- Train operators and workers, and maintain training records
- Maintain inventory of machine accessories and change parts
- Provide requisition & review of BMRs and BPRs to the QA department
- Update KPIs and investigate root cause analysis of identified problems
- Report near miss incidents to Human Resources and safety department
- Plan manpower requirements under the guidance of HOD
- Utilize resources effectively for higher productivity
- Ensure product quality, cleanliness, and compliance with safety measures
- Complete monthly production plan and verify weighing balances
- Coordinate external parties for calibration of instruments
- Prepare documents for ISO 9001:2015, 14001:2015 & 18001:2007 compliance
- Ensure effective sanitation & hygiene activities at all levels
- Report hazards, incidents, accidents, and near misses
Qualifications Required:
- Bachelor of Pharmacy (B.Pharm)
- Full-time availability
(Note: No additional details about the company were provided in the job description.)
Skills Required
Batch manufacturing
Change control
SOP
Deviation
CAPA
PPE
Work permit system
Waste disposal
SOPs
Quality management
Data integrity
Dispensing
Granulation
Compression
Training
Inventory management
Root cause analysis
Manpower planning
Resource utilization
Quality control
Preventive maintenance
Production planning
GMP
QMS documents
QEHS policy
QEHS issues
QEHS nonconformities
Continual improvement projects
cGMP norms
Productivity optimization
Sanitation activities
Manpower allocation
Raw materials verification
Packing materials verification
Coating activities
SAP system
Change parts
BMRs
BPRs
KPIs
Near miss incident reporting
Material segregation
Weighing balances verification
Calibration of instruments
ISO 90012015
ISO 140012015
ISO 180012007
Sanitization
Hygiene activities
Hazards reporting
Accident reporting
Posted on: March 16, 2026
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