Microbiology QC Analyst – cGMP & Sterility Testing

ADP, Inc.; Philadelphia (Philadelphia County); On-site; USD 55,000 - 75,000; Full time

Job summary

ADP, Inc. in Navy Yard, Philadelphia, PA, is seeking a Quality Control Microbiology Associate to support drug safety, quality, and regulatory compliance through routine microbiological testing and monitoring activities.

You will perform in-process environmental monitoring, endotoxin and sterility testing, and stability assessments, while ensuring SOPs and cGMP requirements are followed. The role requires a Bachelor's or Associates degree in a related field and 0–3 years of GMP lab experience.

Qualifications

• GMP knowledge applicable to a quality control lab setting.
• Experience with microbiology methods and data trending.
• Strong attention to detail and ability to maintain data integrity.

Responsibilities

• Perform in-process environmental monitoring of cGMP manufacturing suites.
• Execute endotoxin and sterility testing per SOPs.
• Conduct stability testing to assess product quality over time.
• Ensure laboratory activities comply with cGMP, FDA and regulatory requirements.
• Document, analyze, and report test results timely with data integrity.
• Assist investigations related to excursions, OOS results, or deviations; support CAPA.
• Collaborate with Manufacturing, QA, and Technical Operations for batch release and regulatory submissions.
• Maintain laboratory equipment and aseptic practices for a safe work environment.

Skills

GMP knowledge

Data analysis

Attention to detail

Documentation

Education

Bachelor’s or Associates degree in Molecular Biology, Biomedical Sciences, Microbiology, or related field

Tools

LIMS

MODA

Job description

ADP, Inc. in Navy Yard, Philadelphia, PA, is seeking a Quality Control Microbiology Associate to support drug safety, quality, and regulatory compliance through routine microbiological testing and monitoring activities.

You will perform in-process environmental monitoring, endotoxin and sterility testing, and stability assessments, while ensuring SOPs and cGMP requirements are followed. The role requires a Bachelor's or Associates degree in a related field and 0–3 years of GMP lab experience.