Bachelor's degree in Mechanical/Electrical Engineering or a related field with 3-5 years of facilities engineering experience. Experience in medical device manufacturing, ideally within cGMP facilities (food, pharma, med devices). Strong knowledge of facilities systems and preventive maintenance programs. In-depth understanding of local building codes, government regulations, and GMP. Experience leading projects, adhering to schedules, and managing timelines. Ability to manage competing priorities in a fast-paced environment. Experience managing critical systems such as Deionized Water, ISO Clean Rooms, Power & Gas, Compressed Gases, Life Safety, Fire Protection, and EBO Building Management. Expertise in system upgrades, end-of-life assessments, and improvements. Knowledge of ISO14644, ISO13408, Clean Room Design, Commissioning, and Qualifications. Familiarity with energy management programs, including ISO50001 and conducting energy audits. Experience preparing for and participating in internal and external quality system audits. Proficiency in preparing design estimates, coordinating with contractors, and managing project execution. Ability to work with engineering firms to develop design criteria and prepare layout and detail drawings.
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