QC Microbiologist

Location: Gulfport MS (fully onsite; relocation required)
Pay: $28.00$35.00/hour

Were 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.

• 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

• 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

• 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

• 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