GMP Technician

Integrated Resources, Inc ( IRI )

Frederick (MD)

On-site

USD 25,000 - 33,000

Full time

12 hours ago
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Job summary

Integrated Resources, Inc (IRI) in Frederick, MD seeks a cGMP Cleaner to perform third-shift cleaning in ISO-classified cleanrooms and CNC lab areas. The role includes garment stocking, inventory management, and adherence to GMP procedures.

The position requires 1+ year in pharma/manufacturing, 100% onsite work, and successful completion of a 3-week training program. Training runs Monday–Friday, with a fixed night schedule.

Qualifications

  • AA degree or HS diploma with 1+ year in pharma/manufacturing.
  • Ability to work 100% onsite in Frederick, MD.
  • Willingness to complete a three-week first-shift training schedule.
  • Experience in cleanroom or cGMP environments preferred.

Responsibilities

  • Perform sanitary cleaning per SOPs and supervisor instructions.
  • Stock, stage, and shift garments in gowning rooms (FIFO).
  • Maintain cleaning/operational records with accuracy.
  • Attend and complete required training per SOPs and policies.
  • Maintain inventory of cleaning supplies and ensure availability.
  • Provide signoff on documentation as required.
  • Support other departments as needed.
  • Work safely per company/state/federal regs.
  • Perform extra tasks as assigned by management.
  • Demonstrate commitment to quality culture.

Skills

On-site work
Third shift
Gowning PPE
Cleanroom protocol
Documentation
Inventory management

Education

AA degree or HS diploma + 1 year exp

Job description

Job Duration: 12+ Months

Work Schedule: 5 Days a Week | 8-Hour Shifts | 3rd Shift

Shift Hours: 10:30 PM – 7:00 AM

Training Schedule: First 3 Weeks, Monday–Friday, 7:30 AM – 4:00 PM

Job Description

The cGMP Cleaner will be responsible for performing third-shift cleaning activities in accordance with cGMP requirements and established operating procedures. The role will also support sterile and non-sterile garment stocking, staging, and inventory management for ISO-classified cleanrooms and Controlled Non-Classified (CNC) laboratory areas.

Key Responsibilities
  • Perform sanitary cleaning activities in accordance with established operating procedures and instructions provided by the Manager/Supervisor.
  • Perform sterile and non-sterile garment stocking, staging, and shifting (FIFO) across multiple gowning rooms.
  • Maintain accurate and complete cleaning and operational records.
  • Attend and complete all required training in accordance with company SOPs, procedures, and policies.
  • Maintain accurate inventory of cleaning supplies and ensure supplies are consistently available.
  • Review documentation and provide signatory signoff as required.
  • Provide accurate and complete support to other departments as needed.
  • Perform all activities safely and effectively in accordance with company, state, and federal regulations.
  • Perform additional tasks and duties as assigned by management.
  • Demonstrate a commitment to the company's quality culture.
Basic Qualifications
  • Associate degree (AA) OR High School Diploma/GED with at least 1 year of experience in operations, pharmaceutical, biotechnology, or manufacturing environments.
  • Ability to work 100% onsite in Frederick, MD.
  • Ability to work the assigned third-shift schedule, including one weekend day per week.
  • Ability to complete the required three-week first-shift training schedule.
Physical and Environmental Requirements
  • Ability to wear cleanroom and protective gowning, including goggles, face shields, gloves, and other required PPE.
  • Ability to wear a respirator when working with certain cleaning chemicals.
  • Ability to perform cleaning and operational activities within ISO-classified cleanrooms.
  • Ability to occasionally lift and/or move up to 40 pounds.
  • Ability to squat, bend, kneel, and reach for approximately 80% of the shift.
  • Ability to stand, walk, and move around for approximately 80% of the shift.
Preferred Qualifications
  • Previous cleanroom sanitization or cleaning experience.
  • Experience working in a cGMP-regulated pharmaceutical, biotechnology, or manufacturing environment.
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