Quality Control Analyst, Microbiology Lab

Johnson & Johnson; Athens (GA); On-site; USD 55,000 - 85,000; Full time

Job summary

Johnson & Johnson in Athens, Georgia seeks an Analyst Quality Control to support environmental monitoring and microbiology testing. The role involves operating lab equipment, maintaining records, ensuring cGMP compliance, and contributing to continuous improvement within the QC unit.

The successful candidate will have a 4-year degree in microbiology or 0–2 years of related experience, strong technical writing, and the ability to work with cross-functional teams to uphold product quality and

Qualifications

• Requires 0–2 years of experience or commensurate 4 year degree in microbiology or closely related field of study.
• Familiarity with cGMPs, FDA regulations, and quality systems is preferred.
• Strong analytical and documentation skills in a controlled environment.

Responsibilities

• Designs, executes, and documents environmental and water system monitoring programs.
• Operates and maintains laboratory equipment with calibrated precision.
• Prepares microbiological media, reagents, and maintains lab records.
• Ensures compliance with cGMP and safety policies; supports investigations and CAPA actions.
• Interprets test results and communicates findings to manufacturing and QA teams.
• Assists in training microbiology personnel and performs data reviews.
• Oversees inventory of lab supplies and proper handling of controlled substances.
• Prepares environmental monitoring reports and risk assessments.

Skills

Quality control

Aseptic techniques

cGMP compliance

Education

B.S. in Microbiology

Tools

Microsoft Office

Job description

Johnson & Johnson in Athens, Georgia seeks an Analyst Quality Control to support environmental monitoring and microbiology testing. The role involves operating lab equipment, maintaining records, ensuring cGMP compliance, and contributing to continuous improvement within the QC unit.

The successful candidate will have a 4-year degree in microbiology or 0–2 years of related experience, strong technical writing, and the ability to work with cross-functional teams to uphold product quality and