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CGMP Cleaning Technician

Job in Longmont, Boulder County, Colorado, 80502, USA
Listing for: Kelly Services
Full Time position
Listed on 2026-10-09
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Manufacturing & Industrial Operations
Salary/Wage Range or Industry Benchmark: 24 - 30 USD Hourly USD 24.00 30.00 HOUR
Job Description & How to Apply Below
Job Description

Job Description Kelly Science and Clinical is leading the search for a capable cGMP clean-room cleaning technician to support Manufacturing Operations for a game-changing biotech customer. Work will be done in a newly constructedearly-stagecell/gene therapyGMPmanufacturing facility.

Job Title:cGMP Cleaning Technician
Location:Louisville, Colorado (80027)
Rate
: $24-30/hr. (commensurate with experience)
Duration
: 9-12 months
Shift
: 6am-2pm | Mon-Fri

POSITION SUMMARY
Ensuring that we produce products in a highly controlled environment of which cleaning is an essential duty.

Primary job responsibilities include, butarenot limited to following SOPs to prepare cleaning solutions, perform dailyroutinecleaningas well as return to service cleaning of clean-room areas and document cleaning on area logbooks.

The role requires attention to detail, the ability to read and directly follow Standard Operating Procedures as well ascomply with Safety procedures and work practices.

Under the supervision of the Manufacturing supervisor, the cleaning team will coordinate scheduling of cleaning activities and work with Quality to ensure tasks are completed and documented per the procedures.

CORE ACCOUNTABILITIES
Specific responsibilities include:

  • Prepare, execute and clean-up after required cleaning activities within the Controlled spaces of the CLIMB.
  • Directly follow and execute the role percontrolleddocumentsand standard operating procedures on behalf of Manufacturing Operations
  • Ability to work wearing clean-roomgowning materials
  • Adheres to Standard Operating Procedures, good manufacturing practices, and good documentation practices
  • Performsandparticipatesin equipment,process,and systemvalidationactivities including Environmental Monitoring Performance Qualification  (EMPQ) and return to service activities
  • PerformscGMP cleaningin an asepticclean-room environment (ISO5, ISO7, ISO8, ISO9)
  • Maintains inventory and performsstocking activities for gowning, cleaning, and consumable materials to ensure sufficient inventory is available to support manufacturing operations
  • Ensures development of operating schedules and ensures schedule adherence for manufacturing taskexecution
  • Other duties as needed

Required Qualifications:

  • High schooldegreeor equivalent
  • 1 yearof cGMPclean-room cleaning experience in the pharmaceutical, biologics and/or medical device field is desired or equivalent in work experience or education

Preferred Qualifications:

  • Demonstrated experience working on results-oriented teams where contribution and collaboration were critical to project success
  • Proficient in computer applications such as word processing, spreadsheets, and web-based applications
  • Self-motivatedwithstrongorganization and communication skills and can work independently

Physical Requirements:

  • Ability togown asepticallyandwork in a Clean Room environment
  • Ability to work while gowned for extended periods oftime
  • Ability to work while reaching and working overhead performing repetitive tasks
  • Extensive useandhandlingofchemicals and biological materials
  • Must have the ability to work around laboratories, manufacturing areasand equipment, and regularly lift 10-20lbs. andperiodicallylift upto 50lbs.
  • Abilityto work nights and weekends as needed
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