Assistant Manager, Mechanical Engineering
About this role
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:
Company at a glance
Amneal Pharmaceuticals, Inc. (NASDAQ: AMRX) is guided by a simple belief: essential medicines should be accessible to everyone. What began as a promise to deliver high-quality, affordable medicines has evolved into a diversified portfolio spanning complex generics and injectables, biosimilars, and specialty medicines, including more than 290 products, with scale and capabilities that help reach patients across the healthcare system while combining world-class precision with a deep sense of personal responsibility for every dose we deliver.
Content is for informational purposes only and 3rd party content does not reflect Amneal’s opinions.
Amneal has the right to remove comments that violate another’s copyright or intellectual property, mention an Amneal product, use profanity or are defamatory, promote and solicit for third-party sites, initiatives, or products, or are factually inaccurate or misleading or spam.
Amneal recommends that you consult with your healthcare provider regarding personal health matters. To report a product complaint or adverse event related to an Amneal product, contact Drug Safety at 877-835-5472, option 3 or [email protected]. If you are currently experiencing a life-threatening event, please immediately contact 911.
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