Assistant Manager - Maintenance
Location: Goa, India
Employment Type: Full-Time
Company: Pfizer
Position Summary
The Assistant Manager - Maintenance is responsible for ensuring the reliability, availability, and optimal performance of manufacturing equipment and facility systems within a GMP-regulated pharmaceutical environment. The role focuses on preventive and predictive maintenance, equipment reliability, root cause investigations, asset lifecycle management, engineering projects, and compliance with cGMP, EHS, and quality standards.
Key Responsibilities
Maintenance & Reliability Engineering
Oversee maintenance and reliability activities for manufacturing equipment and facility systems.
Execute preventive, predictive, and breakdown maintenance programs.
Ensure high equipment uptime and operational efficiency.
Develop and optimize maintenance strategies for critical assets.
Equipment Performance & Troubleshooting
Lead Root Cause Failure Analysis (RCFA) investigations for equipment failures.
Implement Corrective and Preventive Actions (CAPA) to improve reliability.
Troubleshoot equipment issues and support rapid problem resolution.
Monitor equipment performance and identify improvement opportunities.
Asset Management & Engineering Support
Support equipment installation, modification, and engineering projects.
Prepare technical specifications and scopes of work for new equipment.
Manage equipment lifecycle activities including commissioning and decommissioning.
Support qualification activities including IQ, OQ, and PQ.
Operational Excellence & TPM
Drive Total Productive Maintenance (TPM) initiatives.
Improve Overall Equipment Effectiveness (OEE) and asset utilization.
Support continuous improvement and reliability engineering programs.
Contribute to energy optimization and cost reduction initiatives.
Compliance & Documentation
Ensure compliance with cGMP, SOPs, and regulatory requirements.
Prepare and maintain maintenance records and technical documentation.
Develop and review SOPs, risk assessments, and engineering procedures.
Support audit readiness and inspection activities.
Safety & Cross-Functional Collaboration
Promote Environmental Health & Safety (EHS) standards and safe work practices.
Conduct risk assessments including FMEA and Quality Risk Assessments (QRA).
Collaborate with Production, QA, QC, Engineering, and external vendors.
Support facility and fire & life safety compliance programs.
Educational Qualification
Bachelor's Degree in Mechanical Engineering.
Experience Required
6–8 years of experience in pharmaceutical manufacturing or GMP-regulated industries.
Hands-on experience with maintenance of pharmaceutical manufacturing equipment.
Experience with tablet compression machines, granulation systems, and packaging equipment.
Exposure to reliability engineering and maintenance management systems preferred.
Technical Skills
Maintenance Engineering
Reliability Engineering
Preventive Maintenance (PM)
Predictive Maintenance (PdM)
Breakdown Maintenance
Root Cause Failure Analysis (RCFA)
Root Cause Analysis (RCA)
Corrective & Preventive Actions (CAPA)
Equipment Troubleshooting
Equipment Lifecycle Management
Asset Management
Total Productive Maintenance (TPM)
Overall Equipment Effectiveness (OEE)
Equipment Reliability Programs
Commissioning & Qualification
GMP Manufacturing Equipment Maintenance
Validation & Compliance
cGMP Compliance
SOP Management
IQ (Installation Qualification)
OQ (Operational Qualification)
PQ (Performance Qualification)
Quality Risk Assessment (QRA)
Failure Modes and Effects Analysis (FMEA)
Audit Readiness
Regulatory Compliance
Equipment Expertise
Tablet Compression Machines
Granulation Systems
Packaging Equipment
Utility Systems
Facility Infrastructure
Manufacturing Equipment
HVAC Systems (Preferred)
Utility Equipment (Preferred)
Software & Systems
AutoCAD
Maintenance Management Systems (CMMS)
Microsoft Excel
Microsoft Word
Microsoft Outlook
P&ID Interpretation Tools
Automation & Process Control Systems (Basic Knowledge Preferred)
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