Microbiologist

Accentuate Staffing is partnering with a leading pharmaceutical manufacturing company that is hiring for a Microbiologists to join their team. This is a contract-to-hire opportunity offering competitive pay and the opportunity to work in a highly regulated GMP manufacturing environment. The ideal candidate has strong environmental monitoring experience, hands‑on sterility and endotoxin testing expertise, and experience conducting investigations within a pharmaceutical setting. Multiple shifts available: 1st shift: Monday to Friday 6am to 2:30pm 2nd shift: Monday to Friday 10am to 6:30pm 3rd shift: Monday to Friday 6pm to 2:30am Responsibilities Perform microbiological testing including bioburden, endotoxin (kinetic turbidimetric & gel clot), particulate matter, and 14-day sterility testing in accordance with USP and internal SOPs. Conduct environmental monitoring in classified cleanroom environments (viable/non-viable air sampling, surface sampling, personnel monitoring). Perform facility water system and clean steam sampling, including microbial and endotoxin testing. Enter, review, and trend laboratory data within LIMS; identify atypical results and elevate as needed. Conduct OOS, OOT, and deviation investigations; support root cause analysis and documentation. Assist with CAPA implementation and continuous improvement initiatives. Support cleaning validation, process validation, and special microbiological studies. Maintain laboratory equipment including autoclaves, glassware washers, particle counters, and isolator systems. Participate in internal audits and regulatory inspections as required. Train and mentor junior analysts on microbiological techniques and GMP compliance. Requirements Bachelor’s degree in Microbiology, Biology, or related life science. 4+ years of microbiology laboratory experience in a GMP-regulated pharmaceutical or biotech environment. Hands‑on experience with environmental monitoring in cleanrooms (ISO classified environments preferred). Experience with LAL testing (kinetic & gel clot), sterility testing, filtration methods, and particulate matter testing. Strong working knowledge of cGMPs, USP standards, FDA regulations, and GLPs. Experience conducting investigations (OOS/OOT), writing reports, and supporting CAPAs. Proficiency with LIMS systems and Microsoft Office (Excel, PowerPoint, etc.). Strong written and verbal communication skills with ability to collaborate cross‑functionally. #J-18808-Ljbffr