Junior Microbiologist - Hands-On QC in Pharma (Full-Time)

Core Environmental Monitoring Lab LLC; Harrisburg (Dauphin County); On-site; USD 17,000 - 25,000; Full time

Job summary

Core QC in Harrisburg, PA is seeking a motivated Microbiologist to join our Quality Control laboratory team. The role offers hands-on training in pharmaceutical microbiology, testing, and laboratory operations, ideal for recent graduates.

You will work alongside experienced professionals, perform routine microbiological testing per USP workflows, maintain records, and contribute to cGMP compliance in a clean, safety-focused environment.

Qualifications

• Bachelor's or master's degree in Microbiology, Biology, Biotechnology, or related life science field.
• Basic knowledge of microbiology and aseptic laboratory techniques.
• Familiarity with cGMP and GLP is preferred.

Responsibilities

• Assist with routine microbiological testing, including USP <797> workflows, bioburden, sterility testing, antimicrobial effectiveness testing (AET), growth promotion testing, and environmental monitoring.
• Prepare culture media, reagents, and laboratory materials following established SOPs.
• Collect, prepare, and process laboratory samples using aseptic techniques.
• Maintain accurate laboratory records and testing documentation.
• Operate, clean, and maintain laboratory equipment.
• Follow cGMP guidelines and laboratory safety procedures.
• Support quality control activities and laboratory investigations.
• Maintain a clean and organized laboratory environment.

Skills

Microbiology basics

Aseptic techniques

Attention to detail

Education

Bachelor's or Master's in Microbiology or related life science

Job description

Core QC in Harrisburg, PA is seeking a motivated Microbiologist to join our Quality Control laboratory team. The role offers hands-on training in pharmaceutical microbiology, testing, and laboratory operations, ideal for recent graduates.

You will work alongside experienced professionals, perform routine microbiological testing per USP workflows, maintain records, and contribute to cGMP compliance in a clean, safety-focused environment.