
Maintenance Engineer
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At a glance
Job overview
Amneal Pharmaceuticals is hiring a Maintenance Engineer. The Maintenance Engineer owns maintenance, troubleshooting, and continuous improvement of manufacturing equipment for oral solid dosage and transdermal systems, ensuring equipment reliability, operational excellence, and cGMP compliance through collaboration with production, quality, engineering, and EHS teams.
Key focus areas include Develop, implement, and optimize preventive and corrective maintenance programs, Diagnose and resolve complex mechanical, electrical, pneumatic, hydraulic, and automation failures, and Lead maintenance, troubleshooting, and repair of manufacturing equipment and utilities.
Important skills include Preventive Maintenance, Troubleshooting, Mechanical Systems, Electrical Systems, Pneumatic Hydraulic, and Automation.
Skills & qualifications
Skills
Full job description
Description:
The Maintenance Engineer will take ownership in all the maintenance, troubleshooting, and continuous improvement of manufacturing equipment and maintenance activities. They play a crucial part in ensuring smooth production of oral solid dosage forms and transdermal systems, including birth control patches. This role demands strong technical expertise, leadership in troubleshooting, and collaboration across departments to ensure operational excellence, equipment reliability, and compliance with cGMP standards.
Essential Functions:
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Develop, implement, and optimize preventive and corrective maintenance programs to maximize equipment uptime and reliability.
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Diagnose and resolve complex mechanical, electrical, pneumatic, hydraulic, and automation-related failures independently.
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Lead the maintenance, troubleshooting, and repair of sophisticated manufacturing equipment including tablet presses, coaters, mixers, dryers, slitters, packaging machines, and utilities.
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Manage and ensure accurate documentation of maintenance activities, maintenance plans, and equipment history within Blue Mountain Regulatory software adhering strictly to GMP and regulatory requirements.
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Lead or assist in equipment installation, qualification, and validation (IQ/OQ/PQ) activities, working closely with validation and quality teams.
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Support root cause analysis (RCA) and lead implementation of corrective and preventive actions (CAPA) related to equipment failures.
Additional Responsibilities:
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Collaborate closely with production, quality assurance, engineering, and EHS teams to support seamless manufacturing operations.
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Manage external contractors and vendors, ensuring adherence to safety and regulatory standards.
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Maintain spare parts inventory levels and suggest reordering as needed.
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Ensure compliance with all health, safety, and environmental standards and company policies.
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Identify and implement continuous improvement initiatives related to equipment reliability, efficiency, and safety.
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