The incumbent is responsible for perform mechanical preventive, corrective and predictive maintenance and troubleshooting pharmaceutical manufacturing equipment. Compliance with industry regulations and participating in the production process. They may perform equipment adjustments / calibrations, assist in validation processes, and contribute to quality control measures within the pharmaceutical manufacturing environment. This role requires a proactive approach, strong problem-solving skills, and the ability to work in a highly regulated environment to support the continuous operation of pharmaceutical manufacturing equipment attention to detail, and adherence to safety protocols. Typical Accountabilities Equipment Maintenance: Responsible for performing mechanical preventive, corrective and predictive maintenance and troubleshooting pharmaceutical manufacturing equipment. Responsible for performing routine maintenance task on manufacturing equipment, including cleaning, lubricating, and adjusting machinery to ensure optimal performance. Assist in the setup and installation of new manufacturing equipment according to specifications and safety guidelines. Conduct regular inspections of machinery to identify potential issues and address them proactively to prevent breakdowns. Collaborate with other team members to complete preventive maintenance schedules and prioritize tasks based on production needs. Assist to coordinate with contractors, the maintenance activities for the above-mentioned equipment’s or support ancillary infrastructure. Troubleshooting: Assist to diagnose and resolve issues with complex mechanical, electrical, and automation systems to minimize downtime and ensure the reliability of pharmaceutical manufacturing processes. Troubleshoot equipment malfunctions and perform repairs as needed to minimize downtime and maintain production efficiency. Documentation: Maintain accurate records of maintenance activities, including logbooks, work orders, and equipment history, ensuring compliance with regulatory standards and GMP requirements. Knowledge of SAP system and transactions required to perform the assigned maintenance activities. Knowledge in the mobile device is required. Collaboration: Work closely with production and quality control teams to address equipment-related concerns, providing technical support and contributing to cross-functional problem-solving efforts. Safety Compliance: Adhere to safety protocols and guidelines while performing maintenance activities, actively promoting a culture of safety within the facility. Training: Stay updated with evolving pharmaceutical technologies and participate in ongoing training programs to enhance knowledge and skills related to equipment maintenance and others development initiatives. Continuous Improvement: Find opportunities for process improvement and efficiency gains, collaborating with engineering teams to implement upgrades or modifications to equipment. Support continuous improvement efforts by providing input on equipment performance and suggesting process enhancements to increase efficiency and quality. Regulatory Compliance: Stay informed about changes in regulatory requirements related to pharmaceutical manufacturing equipment and ensure that all maintenance activities align with industry standards. Emergency Response: Respond promptly to equipment breakdowns and emergencies, implementing corrective actions to minimize production disruptions. The respond includes support to storm emergency site strategy. Spare Parts Management: Maintain an organized inventory of spare parts and collaborate with procurement to ensure timely availability when needed. Systems and digital: Knowledge of SAP system and transactions required to perform the assigned maintenance activities. Knowledge in the mobile device is required. Work with the site Building Management Systems (BMS) to check equipment conditions. Assist technician level 2 and 3 on troubleshooting when the utilities' area is within the assigned scope. Actively promotes compliance with and supports the governance process for deploying standard AZ processes and practices within IPR Lean program and Lean Maturity site strategy.
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Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree
Number of Employees
5,001-10,000 employees