Microbiologist

QualificationsMaster’s degree in Microbiology, Biology, Biotechnology.About the RoleThe Microbiology & Cleaning Validation Associate supports MS&T activities related to microbiological control, cross contamination, cleaning validation and verification, and TOC-based cleanliness assessment for pharmaceutical manufacturing equipment and facilities. This is a hands-on, entry-level role ideal for a recent Master’s graduate with strong microbiology fundamentals and an interest in applied GMP manufacturing environments.The role focuses on sampling execution, data documentation, and on-floor support, risk assessments, investigations, etc. working under the guidance of MS&T scientists and engineers to ensure equipment cleanliness, contamination control, and inspection readiness.ResponsibilitiesPerform microbiological and cleaning validation sampling, including swab and rinse samples.Create and execute protocols for routine cleaning verification and TOC sampling.Apply proper aseptic and low-bioburden handling techniques during sampling activities.Develop and execute TOC-based cleaning validation, including sample handling, data review, and coordination with QC or external laboratories.Assist with microbial and chemical cleanliness risk assessments for equipment and processes.Document sampling activities and results in compliance with GMP and data integrity (ALCOA+) requirements.Support validation, PPQ, and process verification activities during new product introductions and equipment changes.Participate in deviations, investigations, and CAPA support related to cleaning or microbiological events.Collaborate cross-functionally with MS&T, QA, QC, Engineering, and Manufacturing teams. Required SkillsEntry-level position; internships, academic research, or co-op experience in microbiology or GMP environments preferred.Exposure to pharmaceutical manufacturing, quality, validation, or laboratory operations is a plus.Digital literacy with exposure to basic AI/ML and use in day to day work.