GMP QC Microbiology Analyst I (Contract)

Kelly Services; Winston-Salem (NC); On-site; USD 33,000 - 41,000; Full time

Job summary

Kelly Services is seeking a QC Microbiology Analyst I on a contract basis in Winston-Salem, NC. The role supports routine microbiological testing and environmental monitoring within a GMP-regulated manufacturing environment.

You will perform EM, bioburden, endotoxin, and sterility testing, maintain accurate GMP documentation, and assist with equipment qualification; strong attention to detail and teamwork are essential.

Qualifications

• High School Diploma required; degree in Microbiology a plus.
• 1–2 years of relevant microbiology experience.
• GMP-regulated lab experience strongly preferred.
• Basic understanding of cGMP and cleanroom practices.
• Experience with Environmental Monitoring, bioburden, endotoxin, or sterility testing.

Responsibilities

• Perform Environmental Monitoring of GMP-controlled areas.
• Support personnel monitoring during manufacturing operations.
• Perform microbiological testing including bioburden, endotoxin, and sterility testing.
• Enumerate, Gram stain, streak, and isolate recovered organisms.
• Collect and test environmental and utility samples.
• Follow SOPs, work instructions, protocols, and safety requirements.
• Maintain GMP documentation accurately and timely.
• Assist with lab equipment qualification and process improvements.
• Maintain QC laboratory inventory and coordinate material requests.
• Maintain hygiene and aseptic practices for GMP cleanrooms.
• Collaborate with Manufacturing and Quality to support testing and reporting.

Skills

Environmental Monitoring

Documentation skills

Team collaboration

GMP compliance

Microsoft Office

Education

High School Diploma

Associate/Bachelor in Microbiology

Tools

Microsoft Office

LIMS

Job description

Kelly Services is seeking a QC Microbiology Analyst I on a contract basis in Winston-Salem, NC. The role supports routine microbiological testing and environmental monitoring within a GMP-regulated manufacturing environment.

You will perform EM, bioburden, endotoxin, and sterility testing, maintain accurate GMP documentation, and assist with equipment qualification; strong attention to detail and teamwork are essential.