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Maintenance Supervisor (Night Shift)
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QX Global Services Private Limited
Concord, NC (In Person)
$106,912 Salary, Full-Time
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Job Description
Maintenance Supervisor (Night Shift) QX Global Services Private Limited Concord, NC Job Details Full-time $48.80 - $54.00 an hour 1 hour ago Benefits Health insurance Dental insurance 401(k) Paid time off Life insurance Qualifications Manufacturing facility HVAC Water systems Full Job Description Job Overview As a Technical Supervisor, you will lead a team that supports senior technical business leaders through administrative coordination, process improvement, financial oversight, and technical execution within a cGMP-regulated pharmaceutical manufacturing environment. This role combines leadership and technical expertise to ensure preventive maintenance, repairs, documentation, and operational excellence across equipment, building systems, and utility infrastructure that support pharmaceutical manufacturing operations. What You'll Do Act as liaison with technical business leaders, facilities managers, quality, manufacturing, engineering, and other internal and external clients to forecast workload demand, maintenance priorities, shutdown windows, and project deliverables within a regulated pharmaceutical manufacturing facility. Manage, plan, coordinate, schedule, and oversee the workload, deadlines, and day-to-day activities of the support team members to ensure effective delivery of services in accordance with site procedures, safety requirements, cGMP expectations, and operational needs. Support operation, maintenance, troubleshooting, and repair activities for utilities and facility infrastructure, which may include boilers, plant steam, chilled water, heating hot water, compressed air, cooling towers, wastewater systems, domestic water, HVAC support systems, pumps, valves, piping, and related utility equipment. Work with business leaders, manufacturing stakeholders, engineering, and quality representatives to resolve conflicting priorities while minimizing impact to pharmaceutical production, validated systems, and site compliance requirements. Coordinate and supervise the team's daily activities, ensuring work is performed safely, efficiently, and in compliance with applicable SOPs, work instructions, permits, lockout/tagout requirements, and cGMP expectations. Apply advanced knowledge to seek and develop new, better methods for accomplishing both individual and department objectives while maintaining compliance with pharmaceutical manufacturing standards and site quality systems. What You'll Need Experience working in a pharmaceutical, biotechnology, medical device, food, chemical, or other regulated manufacturing environment preferred. Prior experience supporting facility utilities, dark utilities, mechanical systems, or industrial maintenance operations in a manufacturing or critical facility environment preferred Working knowledge of cGMP, Good Documentation Practices, SOP compliance, work order documentation, and regulated maintenance expectations preferred. Meet the physical requirements of this role including stooping, standing, walking, climbing stairs/ladders, working in mechanical spaces, and the ability to lift/carry heavy loads of 50 lbs. or more.