Pharma QC Microbiology Analyst - Quality Impact

ACTalent; Cincinnati (OH); On-site; USD 34,000 - 41,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Paid time off

Job summary

ACTalent seeks a QC Microbiology Analyst to perform microbiological testing on raw materials, in-process and finished products, and environmental samples in a GMP/GLP environment. The role involves media preparation, culture maintenance, and participation in method development and validation projects.

You will collaborate with cross-functional teams to support quality objectives and maintain compliant laboratory records while adhering to safety protocols.

Qualifications

• Bachelor's degree in Microbiology or related field.
• Knowledge of GMP/GLP principles and their application in a lab.
• Experience with microbiology testing and environmental monitoring.
• Strong documentation and data integrity skills.
• Ability to work in a regulated laboratory environment.

Responsibilities

• Perform microbiological testing on raw materials, in-process samples, finished products, and environmental samples in accordance with SOPs, GMP, and GLP requirements.
• Prepare microbiological media and reagents with accurate formulation, labeling, and sterility.
• Maintain and handle microbial cultures following aseptic techniques and safety protocols.
• Conduct environmental monitoring including sampling of air, surfaces, and personnel and interpret results against limits.
• Calibrate, operate, and maintain laboratory equipment to ensure reliable test results.
• Document all laboratory activities and results clearly in notebooks and electronic systems.

Skills

GMP/GLP knowledge

Microbiology testing

Laboratory maintenance

Documentation & record-keeping

Environmental monitoring

Aseptic techniques

LIMS/SAP knowledge

MS Office

Education

Bachelor's degree in Microbiology

Tools

LIMS

SAP

Job description

ACTalent seeks a QC Microbiology Analyst to perform microbiological testing on raw materials, in-process and finished products, and environmental samples in a GMP/GLP environment. The role involves media preparation, culture maintenance, and participation in method development and validation projects.

You will collaborate with cross-functional teams to support quality objectives and maintain compliant laboratory records while adhering to safety protocols.