Cleanroom Microbiology QC Technician

STAQ Pharma

Columbus (OH)

On-site

USD 52,000 - 68,000

Full time

14 days+

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Job summary

STAQ Pharma in Columbus, OH, seeks a Quality Control Microbiology Technician 1 to support clean room operations during batch production and ensure adherence to procedures. You will assist in deviations/investigations and engage in environmental monitoring activities in ISO 7 areas.

The role requires cGMP experience, strong attention to detail, and the ability to work in a fast-paced, small company environment. Proficiency in MS Office and familiar with 21 CFR Part 11 is preferred.

Qualifications

  • Associate or Bachelor's degree in Microbiology, Biology, or related life sciences.
  • Experience in microbiology or quality control preferred.
  • Experience in a cGMP or cleanroom setting preferred.

Responsibilities

  • Ensure clean rooms meet required cleanliness standards.
  • Adhere to gowning and personal hygiene practices to prevent contamination.
  • Perform environmental monitoring in ISO 7 Classified Areas.
  • Support QC investigations and data trending related to environmental monitoring.
  • Train new personnel on enumeration and colony morphology procedures.
  • Assist with data reporting and documentation in investigations.

Skills

cGMP aseptic
Attention to detail
Fast-paced environment
Pharmaceutical experience
MS Office suite
21 CFR Part 11 familiarity

Education

Associate or Bachelor's degree in Microbiology
Quality control experience preferred

Tools

Microsoft Word
Microsoft Excel
PowerPoint
Outlook

Job description

STAQ Pharma in Columbus, OH, seeks a Quality Control Microbiology Technician 1 to support clean room operations during batch production and ensure adherence to procedures. You will assist in deviations/investigations and engage in environmental monitoring activities in ISO 7 areas.

The role requires cGMP experience, strong attention to detail, and the ability to work in a fast-paced, small company environment. Proficiency in MS Office and familiar with 21 CFR Part 11 is preferred.

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