QC Microbiologist

Microbiologist Position Type: Contract Location: Onsite Cary, IL (100% Onsite Laboratory) Schedule: Sunday Thursday, 9:00 AM 5:00 PM Job Overview We are seeking a detail-oriented Contract QC Microbiologist to join our Quality Control team in Cary, IL. This role is 100% onsite and primarily focused on executing hands‑on, routine microbiological testing of raw materials, in‑process solutions, and finished pharmaceutical products within a cGMP laboratory environment. This position involves high-volume, standardized compendial testing (~80% hands‑on laboratory work and ~20% administrative data entry/documentation). Depending on candidate qualifications, responsibilities may also extend to data review and laboratory investigation support. Key Responsibilities Microbiological Testing: Perform routine and non‑routine testing, including bioburden analysis, growth promotion testing (GPT), antimicrobial effectiveness testing (AET), and microbial identifications. cGMP Documentation: Accurately document all test procedures, raw data, and results in real time in strict compliance with cGMP, USP, and data‑integrity standards. Lab Maintenance & Readiness: Maintain laboratory equipment, stock testing reagents/supplies, and ensure general laboratory organization and safety compliance. Data Review & Investigations: Support peer data review, out‑of‑specification (OOS) results, and laboratory deviation investigations based on experience and qualification. Communication & Collaboration: Track testing timelines and proactively communicate test status, equipment issues, or potential delays to laboratory leadership. Qualifications & Requirements Minimum Qualifications Education: Bachelor's Degree in Microbiology, Biology, or a related scientific discipline (Required). Note: Candidates holding a Master's degree or higher will be considered, but must be comfortable with high-volume, repetitive bench execution without research/development duties. Compliance & Detail: Strong understanding of cGMP regulations, data integrity, and strict adherence to standard operating procedures (SOPs). Work Style: High attention to detail, strong technical writing skills, and the ability to work independently following training and qualification. Schedule & Location: Ability to work 100% onsite in Cary, IL on a fixed Sunday through Thursday (9:00 AM 5:00 PM) schedule. Preferred Qualifications Prior hands‑on experience in a cGMP Quality Control microbiology laboratory. Familiarity with compendial testing methodologies (USP/EP/JP). Experience with laboratory data review and OOS/OOT investigation procedures. #J-18808-Ljbffr