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Cleanroom Laboratory Technician

Job in Houston, Harris County, Texas, 77047, USA
Listing for: Katalyst Healthcares & Life Sciences
Full Time position
Listed on 2026-07-01
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Production QC/QA
Job Description & How to Apply Below
Job Description:
We are seeking a Cleanroom Laboratory Technician to support manufacturing and laboratory operations within a regulated production environment. This position is responsible for environmental monitoring, cleanroom support, equipment preparation, documentation, and general laboratory activities to ensure compliance with quality and safety standards.

The ideal candidate has hands-on laboratory experience, strong attention to detail, and the ability to work in a cleanroom while following established procedures.
Responsibilities:

  • Perform environmental monitoring activities in controlled cleanroom environments.
  • Collect, document, and maintain environmental and laboratory data.
  • Support routine laboratory and manufacturing operations using aseptic techniques when required.
  • Prepare buffers, media, and production components following standard procedures.
  • Operate laboratory and manufacturing equipment used in daily production activities.
  • Assist with cleanroom setup, stocking, organization, and maintenance.
  • Complete batch records, laboratory documentation, and production logs accurately.
  • Follow GMP, safety, and quality procedures while maintaining compliance.
  • Coordinate equipment readiness and support routine operational activities.
  • Assist with process improvements and other laboratory duties as assigned.

Requirements:

  • High School Diploma or GED with 1 3 years of laboratory, manufacturing, or cleanroom experience;
    or
  • Bachelor's degree in Biology, Microbiology, Biotechnology, Chemistry, Life Sciences, or a related scientific field.
  • Basic laboratory knowledge and documentation skills.
  • Ability to work in a cleanroom environment while following standard operating procedures.
  • Strong attention to detail and organizational skills.
  • Comfortable standing for extended periods and performing repetitive tasks.

Preferred Qualifications:

  • Experience working in GMP, GLP, pharmaceutical, biotechnology, medical device, or clinical manufacturing environments.
  • Experience with environmental monitoring or aseptic processing.
  • Familiarity with laboratory instruments and cleanroom monitoring equipment.
  • Knowledge of microbiology or cell culture techniques is a plus.
  • Experience completing manufacturing or batch documentation.
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