Position Summary

This position ensures the proper operation and maintenance of all utility systems; takes corrective action and repairs equipment as necessary; provides appropriate notification and documentation of all work performed.  General maintenance on mechanical, electrical, refrigeration and various maintenance and repairs within a GMP manufacturing facility. 

Essential Functions (ES) and Responsibilities

• Ensure utility areas are kept reasonably clean and free of debris or clutter.
• Perform routine Preventive Maintenance on boilers, stills, air compressors, pumps and other assigned equipment.  Generate and maintain the required documentation.
• Perform and document daily rounds observing utility instruments, mechanical, electrical and other various aspects of the facility. Create additional work orders for any abnormal issues observed.
• Assist in plumbing, mechanical, and/or electrical equipment such as: pumps, circuit panels, refrigeration, WFI, boilers, HVAC chillers, air compressors, motors, etc.,
• Handle repairs and maintenance on equipment, as well as assigned work orders.  Notification of appropriate personnel as needed.  Create and maintain necessary documentation of these repairs.
• Adhere to all ADMA SOPs, procedures, policies and federal regulations in the operations of these facilities.

Job Responsibilities or Job Requirements

Competencies

Experience Requirements

1-3 years previous general maintenance and/or construction experience needed, in the pharmaceutical/medical devices industry preferred.  GMPs and ISO regulations knowledge needed for this position. 

Preferred Experience

Compliance Requirements (ES)

• The minimum compliance expectation for this role entails strict adherence to FDA regulations and company policies governing sales and marketing activities. This includes completion of required compliance training, accurate documentation of sales interactions, and adherence to data privacy regulations. Additionally, the role requires proactive participation in compliance reviews, prompt reporting of any potential issues, and ongoing education to stay updated on relevant FDA regulations.