Assistant Manager, Mechanical Engineering

Amneal Pharmaceuticals LLC

India

On-site

INR 1,500,000 - 2,100,000

Full time

6 hours ago

Be an early applicant

Get more replies from employers

Send a job-specific resume in minutes.

Job summary

Amneal Pharmaceuticals LLC is seeking an Assistant Manager of Mechanical Engineering in Ahmedabad. You will lead mechanical systems design, installation, operation and maintenance for pharma manufacturing, ensuring validated, audit-ready equipment and adherence to quality and safety standards.

Responsibilities span project governance, URS preparation, vendor coordination, and continuous improvement, with a focus on GMP compliance and timely delivery across greenfield and brownfield sites.

Qualifications

Bachelor's degree in engineering (B.E./B.Tech) required; Master's degree preferred.
8–12 years of experience in mechanical engineering for pharma/manufacturing.
Knowledge of GMP, EHS, validation and engineering standards.

Responsibilities

Lead multiple greenfield and brownfield projects for equipment, utilities, automation, and facilities.
Define scope, URS, capital approval, planning and governance.
Coordinate with cross-functional teams and consultants for detailed engineering.
Review design-basis docs, P&IDs, and equipment specs.
Manage schedules, procurement, installation, commissioning, and qualification milestones.
Ensure GMP compliance, safety, and quality throughout the project lifecycle.

Skills

Equipment Operation & Maintenance

Change parts & Maintenance

Hazard Identification & Risk

Maintenance Management via CMMS

Mechanical System Troubleshooting

Mechanical Systems Fundamentals

P&ID Design

Preventive & Predictive Maintenance

Process & Trend Analysis

Process Optimization

Safety & Hygiene Practices

Troubleshooting & Maintenance

Education

Bachelor's Degree (B.E/ B.Tech)

Master Degree (M.E)/ M.Tech

Tools

CMMS

Job description

Assistant Manager, Mechanical Engineering

Ahmedabad City, Gujarat, India

Trending

Job Description

Description:

The role is responsible for leading and managing mechanical engineering activities supporting pharmaceutical manufacturing operations. The role ensures design, installation, operation, maintenance, and optimization of mechanical systems and utilities in compliance with quality, safety, regulatory, cost, and performance standards. It involves interpreting engineering drawings, plans, and specifications, overseeing execution, and ensuring validated and audit-ready systems. The role supports resource planning, team guidance, vendor coordination, and continuous improvement initiatives. It contributes to reliable production operations, timely project execution, and engineering governance, while ensuring adherence to established engineering standards, SOPs, and regulatory requirements.

Essential Functions:

Manage multiple greenfield and brownfield engineering projects covering manufacturing equipment, utilities, automation, facility modifications and capacity-expansion initiatives.

Lead project initiation, scope definition, URS preparation, capital approval, project planning, risk assessment and governance.

Participate in conceptual, basic and detailed engineering with user functions, CFTs, engineering consultants and PMC.

Coordinate preparation and review of design-basis documents, layouts, P&IDs, utility requirements, equipment specifications and detailed engineering deliverables.

Lead vendor technical discussions, technical bid evaluation, vendor recommendation, drawing review and execution coordination.

Develop and monitor project schedules, procurement plans, delivery schedules, installation plans, commissioning plans and qualification milestones.

Conduct regular progress reviews, maintain project dashboards and provide structured updates to site and corporate leadership.

Coordinate site readiness, equipment installation, utility integration, automation, commissioning, qualification and formal handover.

Monitor project scope, cost, schedule, risks, changes, safety, quality and documentation throughout the lifecycle.

Ensure compliance with applicable GMP, EHS, validation, company engineering and statutory requirements.

Facilitate timely resolution of cross-functional and vendor-related issues and implement recovery plans for schedule deviations.

Complete project closure through punch-point resolution, as-built documentation, training, spares, warranty and lessons-learned review.

To prepare, review, and approve any document required for design, development, implementation of any of the Projects or required during execution of any activity as per roles and responsibility.

To perform additional tasks as directed by Reporting Manager.

Additional Responsibilities:

Qualifications

Education: