GMP Facility Services Associate

The GMP Facility Services Associate performs cleaning, disinfection, sanitation, and room-readiness activities within Abzena's classified and controlled GMP manufacturing areas.

The role executes approved procedures and completes associated controlled documentation to ensure production spaces remain safe, compliant, organized, and ready to support scheduled manufacturing operations.

The associate works closely with Manufacturing, Quality Assurance, Materials Management, Warehouse Operations, Engineering, Facilities, and other site functions.

This team member is also required to provide trained and authorized assistance within manufacturing and warehouse spaces as operational needs arise, while following all applicable gowning, safety, documentation, material-status, segregation, and contamination-control requirements

· Perform routine, campaign, turnover, and periodic cleaning and disinfection of classified and controlled GMP areas in accordance with approved SOPs, schedules, and area-specific requirements.

· Prepare, label, handle, rotate, and use cleaning agents and disinfectants in accordance with approved procedures, safety data sheets, expiration requirements, and established contact times.

· Complete cleaning records, logbooks, checklists, labels, and other controlled documentation accurately, legibly, contemporaneously, and in accordance with data-integrity expectations.

· Inspect assigned areas before and after cleaning and promptly report damage, residue, leaks, pest activity, supply shortages, documentation errors, or other conditions that could affect safety, compliance, or room readiness.

· Use dedicated tools and equipment correctly and maintain required segregation between classified areas, process areas, and non-classified spaces.

· Clean, inspect, store, and maintain mops, buckets, vacuums, carts, floor-care equipment, and other assigned tools in accordance with approved procedures.

· Maintain cleaning supplies, PPE, consumables, and disinfectant inventory at designated points of use and notify the supervisor of shortages or expiring materials.

· Follow cleanroom behavior, gowning, material-transfer, line-clearance, waste-removal, and access-control requirements for each assigned area.

· Immediately notify the supervisor and Quality Assurance of missed cleaning, spills, excursions, damaged equipment, documentation errors, or other potential quality events.

· Participate in investigations, retraining, corrective actions, change controls, risk assessments, and continuous-improvement activities related to GMP facility services.