QC Microbiologist

QC Microbiologist Location: Gulfport, MS (fully onsite; relocation required) Pay: $28.00–$35.00/hour About the Role We're looking for experienced QC Microbiologists to join a GMP-regulated pharmaceutical laboratory supporting the manufacture of human and veterinary drug products. This hands-on position involves microbiological testing of raw materials, in-process materials, finished products, environmental samples, and stability samples. Strong attention to detail, sound microbiological technique, and familiarity with cGMP practices are essential. What You'll Do Perform routine microbiological testing on raw materials, in-process materials, finished products, stability samples, water, and other samples Conduct environmental monitoring, including sampling, testing, documentation, and interpretation of results Perform microbial enumeration, microbial limits, bioburden, and other required assays Prepare culture media, reagents, and solutions; perform media sterilization and growth promotion/suitability testing Support microbial identification and related investigations Perform sterility, endotoxin, or other microbiological quality control testing as applicable Participate in method qualifications, validations, and transfers Operate, clean, and maintain laboratory equipment and instrumentation Accurately document lab activities, observations, and results per established procedures Review analytical and microbiological data for accuracy and compliance Investigate and troubleshoot unexpected results, test issues, or equipment problems Support lab investigations, deviations, change controls, and CAPAs Maintain lab cleanliness, organization, and contamination control Collaborate with Quality, QC, and Manufacturing teams Train and mentor newer laboratory staff as needed What You'll Need 3+ years of hands-on microbiology lab experience, ideally in a pharmaceutical, biopharmaceutical, veterinary pharmaceutical, or other GMP-regulated setting Practical experience with microbiological testing in a QC lab Experience in one or more of: environmental monitoring, microbial limits, bioburden, sterility testing, endotoxin testing, microbial identification, or water testing Working knowledge of cGMP laboratory practices Understanding of quality systems, including deviations, investigations, change controls, and CAPAs Strong aseptic technique and contamination control awareness Accurate documentation skills and strong written/verbal communication Solid organizational skills, attention to detail, and ability to manage multiple priorities Ability to work independently and as part of a team Education & Experience Degree in Microbiology, Biology, Biochemistry, or a related field preferred (equivalent hands-on experience considered) GMP-regulated pharmaceutical or life sciences lab experience strongly preferred Familiarity with laboratory information systems and Microsoft Office is a plus Physical Requirements Able to lift up to 50 lbs. as needed Able to stand, walk, or sit for extended periods (8+ hours/day) Able to work in a lab environment following safety and contamination‑control procedures #J-18808-Ljbffr