AM/Manager Engineering Operations & Maintenance - Sterile - Pune

Emcure Pharmaceuticals Limited

Pune District

On-site

INR 4,000,000 - 5,500,000

Full time

3 days ago
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Job summary

Emcure Pharmaceuticals Limited is seeking an Engineering Manager to lead Sterile Manufacturing engineering operations, maintenance and asset lifecycle management for PFS, ADC and vial filling lines in Pune. You will drive reliability, compliance with MHRA/EU GMP/WHO GMP and oversee qualification, validation and capex projects with a strong focus on safety and GMP adherence.

You will manage a team of engineers, supervisors and technicians, coordinating with QA, production and regulatory teams to

Qualifications

  • Experience in regulated pharmaceutical companies such as Injectable, Biologics, Sterile, Vaccine, PFS or ADC manufacturing facilities.
  • Hands-on exposure to filling lines.
  • Experience handling engineering support for sterile facilities inspected by MHRA, EMA or equivalent regulatory bodies.

Responsibilities

  • Lead preventive, predictive, breakdown and reliability maintenance for sterile manufacturing equipment.
  • Monitor KPIs such as MTBF, MTTR, OEE, downtime and maintenance compliance.
  • Manage utilities including HVAC, water systems, pure steam, compressed air, chillers and electrical distribution.
  • Lead qualification and validation activities (DQ/IQ/OQ/PQ) for equipment and utilities.
  • Drive capex projects, vendor selection, budgeting and execution.
  • Lead installation, commissioning, start-up of new equipment and facilities.
  • Lead engineering team performance reviews and development, ensuring GMP practices.

Skills

Sterile Manufacturing Engineering
PFS, ADC & Vial Line Operations
HVAC & Cleanroom Systems
WFI & Pure Steam Systems
Equipment Qualification & Validation
CAPEX Project Management
Reliability Engineering
GMP Compliance
Regulatory Audit Handling
Team Leadership
Root Cause Analysis
SAP PM / CMMS

Education

BE / BTech (Mechanical, Electrical, Instrumentation or Equivalent)

Tools

SAP PM / CMMS

Job description

Job Description Engineering Manager (Sterile Manufacturing)

Position: Engineering Manager
Department: Engineering
Location: Pune
Qualification: B.E. / B.Tech (Mechanical, Electrical, Instrumentation or Equivalent)
Experience: Minimum 10 Years in Pharmaceutical Manufacturing Engineering, including at least 2 Years in a Managerial Role within a Regulated Pharmaceutical Company.

Job Purpose

To lead engineering operations and maintenance activities for Sterile Manufacturing facilities, ensuring maximum equipment reliability, regulatory compliance, asset lifecycle management, and uninterrupted production support for PFS (Pre-Filled Syringes), ADC (Antibody Drug Conjugate), and Vial Filling Lines.

Key Responsibilities
Engineering Operations & Maintenance
  • Lead preventive, predictive, breakdown, and reliability maintenance activities for sterile manufacturing equipment.
  • Ensure high equipment uptime and operational efficiency of:
    • Pre-Filled Syringe (PFS) Lines
    • Vial Filling & Stoppering Lines
    • Isolators and RABS Systems
    • Lyophilizers
    • Autoclaves
    • CIP/SIP Systems
    • Visual Inspection Machines
    • Packaging Equipment
  • Monitor engineering KPIs such as MTBF, MTTR, OEE, downtime, and maintenance compliance.
Utilities & Facility Management
  • Manage critical utilities including:
    • HVAC Systems
    • Water Systems (PW & WFI)
    • Pure Steam Generators
    • Compressed Air Systems
    • Chillers & Cooling Towers
    • Electrical Distribution Systems
    • BMS & EMS Systems
  • Ensure uninterrupted utility support for sterile manufacturing operations.
Regulatory & Compliance Management
  • Ensure compliance with:
    • MHRA
    • EU GMP
    • WHO GMP
    • Schedule M
    • Data Integrity Requirements
  • Support and lead engineering activities during regulatory audits and customer inspections.
  • Ensure compliance of maintenance and engineering documentation.
Qualification & Validation
  • Lead execution of:
    • DQ, IQ, OQ and PQ activities
    • Equipment Qualification
    • Utility Qualification
    • Facility Qualification
  • Support Validation, Quality Assurance and Production teams during qualification projects.
Projects & Automation
  • Lead installation, commissioning, qualification, and startup of new equipment and facilities.
  • Manage capex projects, vendor selection, budgeting, and execution.
  • Drive automation and digitalization initiatives to improve operational efficiency.
Team Management
  • Lead and develop engineering team members, supervisors, and technicians.
  • Conduct performance reviews, capability development and succession planning.
  • Ensure adherence to safety and GMP practices across the engineering team.
EHS & Risk Management
  • Ensure compliance with safety standards and engineering best practices.
  • Participate in risk assessments, HAZOP studies, and investigation of engineering-related deviations.
Desired Experience
  • Experience in regulated pharmaceutical companies such as Injectable, Biologics, Sterile, Vaccine, PFS, or ADC manufacturing facilities.
  • Hands-on exposure to filling lines
  • Experience handling engineering support for sterile facilities inspected by MHRA, EMA or equivalent regulatory bodies.
Key Skills
  • Sterile Manufacturing Engineering
  • PFS, ADC & Vial Line Operations
  • HVAC & Cleanroom Systems
  • WFI & Pure Steam Systems
  • Equipment Qualification & Validation
  • CAPEX Project Management
  • Reliability Engineering
  • GMP Compliance
  • Regulatory Audit Handling
  • Team Leadership
  • Root Cause Analysis
  • SAP PM / CMMS
Reporting

Reports To: Engineering Head

Team Size

Managing Engineering Team comprising Engineers, Supervisors, Technicians and Utility Personnel.

Preferred Industry: Injectable, Biologics, Vaccines, Oncology, ADC, Sterile Pharma Manufacturing Facilities.

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