QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you'll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA. Responsibilities: + Support the maintenance, operation, and repair of all manufacturing equipment within the client's facility + Provide support to engineering and operations in the design, installation, testing, operation, and maintenance of manufacturing and support equipment + Ensure all assigned equipment and associated subsystems are maintained in accordance with Federal, State, Local, and Amgen regulations, procedures, and policies + Maintain all assigned equipment areas in a constant state of inspection readiness + Identify training deficiencies and provide recommendations and training where applicable + Continuously evaluate and improve maintenance practices and documentation + Perform troubleshooting of electrical, pneumatic, and mechanical equipment + Complete preventive maintenance and assigned paperwork following all cGMP documentation guidelines + Coordinate contractors for repairs, modifications, and installations of equipment + Work directly with Manufacturing, Engineering, and Quality organizations on new system installations or modifications + Attend all required cGMP and Safety training Qualifications: + Associate degree and 4 years of experience + Thorough working knowledge of pharmaceutical packaging equipment operation, maintenance, and repair + Full working knowledge of pumps, valves, motors, and proper lubrication + Full working knowledge of cGMP and Predictive Maintenance philosophy and techniques + Ability to create, read, interpret, and revise engineering documents + Strong writing skills for preparing technical reports and documentation + Ability to identify and implement process improvements + Ability to read and understand P&IDs, work from SOPs, and use basic computer skills + Knowledge of and ability to use Computerized Maintenance Management Systems (Maximo) + Ability to lift up to 50 pounds, climb ladders, and work at elevations up to 15 feet + 2+ years of experience in manufacturing maintenance is ideal. + Experience in a GMP-regulated environment. + Day shift - 7-3:30 or 8-4:30 + The team may shift to 12-hour days working 3-4 days per weeks. + Flexible within day shift hours. Potential overtime opportunities. Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law. Powered by JazzHR
Job ID: 473594937
Originally Posted on: 4/16/2025
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