Quality Control Microbiology Technician

Staq-Pharma; Columbus (OH); On-site; USD 28,000 - 39,000; Full time

Job summary

STAQ Pharma, Inc. is seeking a Quality Control Microbiology Technician in Columbus, OH to support clean room operations and batch production.

The role emphasizes adherence to cGMP, gowning, and routine environmental monitoring across ISO 7 classified areas, with collaboration on investigations and data reporting.

Qualifications

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

Responsibilities

• Ensure clean rooms and related areas meet cleanliness standards as per procedures.
• Adhere to gowning and personal hygiene practices to prevent contamination.
• Monitor clean room equipment and perform environmental monitoring in ISO 7 areas.
• Collaborate with production to resolve quality issues and ensure documentation is complete.
• Collect, submit, and manage microbiological samples to testing laboratories.
• Generate data reports from internal EM results or external tests.

Skills

cGMP aseptic manufacturing

Attention to detail

Fast-paced environment adaptability

Pharmaceutical experience preferred

MS Office proficiency

21 CFR Part 11 familiarity

Education

Associate or Bachelor’s degree in Microbiology or Biology

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Microsoft Outlook

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Quality Control Microbiology Technician

Quality Full Time Columbus, OH, US

2 days ago Requisition ID: 1402

Job Summary:

Quality Control Microbiology Technician 1 will provide clean room support for batch production and ensuring procedure adherence during filling of product. Utilize appropriate controlled documents and assist in quality control deviations/investigations.

Responsibilities:

• Ensure clean rooms and associated areas meet the required cleanliness standards as per company procedures.
• Adhere to strict gowning and personal hygiene practices to prevent contamination and maintain integrity of the clean room environment.
  • Perform gowning qualification training for individuals from all departments who must enter ISO 7 classified areas.
• Monitor and maintain clean room equipment such as viable and non-viable samplers to ensure optimal performance and compliance with established standards.
  • Perform and lead routine environmental monitoring activity in ISO 7 Classified Areas
• Work with production to resolve Quality issues and ensure documentation is complete.
• Perform routine and non-routine viable, non-viable and surface environmental monitoring in all classified areas of the facility.
• Incubation and enumeration of samples related to environmental monitoring processes.
  • Train new personnel on enumeration activities
• Evaluate organisms by colony morphology and perform subculturing.
  • Train new personnel on colony morphology assessment and subculturing activities.
• Continuous improvement activities for environmental monitoring program.
• Provide quality control and microbiology support for operations.
• Collect, submit and manage microbiological samples to third party testing laboratories.
• Generate data reports and/or other compliant documentation from internal EM resultsor external testing results.
• Maintain timely assembly, reporting,and review of all routine and production environmental monitoring results and release testing resultsgenerated.
• Assist with QC Microbiologists (and other investigators) with investigations as they relate to environmental monitoring or other quality control deviations.
• Assist QC Microbiologists with data trending and data reporting as they relate to environmental monitoring or other data-generating processes.
• Perform routine testing or cleaning associated with the BioSafety Cabinet.
  • Lead and train new personnel on the cleaning procedures and testing procedures carried out in the BioSafety Cabinet
• Assist in process, procedural, equipment issues via experimentation or revision of procedures.
• Other duties as assigned.

Required Skills/Abilities: (examples)

• Experience with cGMP aseptic manufacturing environment.
• Strong attention to detail.
• Comfortable in a fast-paced, small company environment and able to adjust workload based upon changing priorities.
• Preferred previous pharmaceutical experience.
• Proficient in using Microsoft Word, Excel, PowerPoint, Outlook.
• Familiarity with 21 CFR Part 11/210/211

Education and Experience:

• 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.

Physical Requirements:

• Prolonged periods of sitting at a desk or laboratory bench and working on a computer.
• Must be able to lift up to 50 pounds at times.

The application window for this position is anticipated to be open at least 25 days