Job Title: Executive – Production
Location: Turbhe, Navi Mumbai, Maharashtra
Business Unit: Piramal Pharma Solutions (PPS)
Employment Type: Full-Time
Department: Production
About Piramal Pharma Solutions
Piramal Pharma Solutions (PPS) is a leading Contract Development and Manufacturing Organization (CDMO) providing integrated drug development and manufacturing services across the pharmaceutical product lifecycle. Through a global network of facilities across North America, Europe, and Asia, PPS supports innovator and generic pharmaceutical companies with comprehensive solutions ranging from drug discovery to commercial manufacturing.
Position Overview
We are seeking a highly motivated Executive – Production to support and oversee day-to-day manufacturing operations within the production department. The role is responsible for ensuring smooth production execution, regulatory compliance, manpower management, documentation accuracy, and adherence to GMP and safety standards.
The ideal candidate should possess strong production operations knowledge, experience in pharmaceutical manufacturing environments, and a thorough understanding of batch documentation and compliance requirements.
Key Responsibilities
Production Operations
Execute and supervise daily manufacturing activities as per approved production plans.
Ensure production activities are completed within defined timelines and quality standards.
Monitor shop-floor operations to maintain productivity, safety, and operational efficiency.
Coordinate production schedules to achieve departmental objectives.
Manpower Management
Allocate manpower based on production priorities and operational requirements.
Assign work responsibilities according to employee skills and competencies.
Monitor workforce utilization and productivity on the production floor.
Guide and support operators and workmen during manufacturing activities.
Material Management
Issue raw materials as per approved production requirements.
Ensure proper documentation of material issuance and consumption.
Monitor material utilization and minimize wastage during manufacturing.
Coordinate with warehouse and planning teams for material availability.
Documentation & Compliance
Maintain production records and documentation in compliance with GMP requirements.
Issue, review, and control production-related documents.
Ensure documentation is accurate, complete, and audit-ready.
Adhere to internal quality systems and regulatory guidelines.
Batch Record Review
Review executed Batch Manufacturing Records (BMR).
Verify Batch Equipment Cleaning Records (BECR) for completeness and accuracy.
Ensure compliance with regulatory and quality standards during record review.
Identify documentation discrepancies and coordinate corrective actions.
Equipment Cleaning & Line Clearance
Monitor equipment cleaning activities and ensure compliance with approved procedures.
Verify cleaning records and line clearance documentation.
Ensure production equipment is maintained in a validated state.
Safety & Work Permit Management
Process and manage work permits in accordance with plant safety requirements.
Ensure all activities are properly authorized before execution.
Promote a strong safety culture across production operations.
Ensure compliance with EHS (Environment, Health & Safety) guidelines.
Quality & Regulatory Compliance
Ensure adherence to cGMP, GDP, SOPs, and regulatory requirements.
Support internal audits, customer audits, and regulatory inspections.
Participate in deviation investigations, CAPA implementation, and continuous improvement initiatives.
Maintain high standards of quality and compliance throughout manufacturing operations.
Required Qualifications
Education
B.Pharm
M.Pharm
B.Sc Chemistry
M.Sc Chemistry
Chemical Engineering
Pharmaceutical Technology
Related Science Discipline
Experience
2–6 Years of experience in pharmaceutical production/manufacturing operations.
Experience in API, formulation, or regulated manufacturing environments preferred.
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