Microbiology & Cleaning Validation Associate

This range is provided by Aequor. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range : $25.00/hr - $35.00/hr Location : Davie, FL Duration : 09+ months with possible extension Shift Schedule : Monday to Friday 8am – 5 pm Temp to Perm role : Possibility based on worker’s performance and openings Core essential skill sets candidates must have to be considered for the role: Recent Master’s graduate Digital literacy with exposure to basic AI/ML and use in day-to-day work Foundational understanding of: Microbiology principles, contamination control, aseptic and low-bioburden handling practices Awareness of: Swab and rinse sampling techniques including environmental monitoring, TOC (Total Organic Carbon) principles and applications in cleaning verification, rapid analytical techniques Strong documentation, attention to detail, and data integrity mindset Job Description The 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; and more. The Associate works under the guidance of MS&T scientists and engineers to ensure equipment cleanliness, contamination control, and inspection readiness. Key Responsibilities Perform 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. Education Master’s degree in Microbiology, Biology, or Biotechnology. Qualifications Entry-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. Foundational knowledge of microbiology principles, contamination control, aseptic and low-bioburden handling practices. Proficiency in swab and rinse sampling techniques, environmental monitoring, TOC principles, and rapid analytical techniques. Strong documentation, attention to detail, and data integrity mindset. Comfortable working in manufacturing and controlled environments. Strong communication and teamwork skills. Willingness to support off‑shift or weekend activities as needed during validations or campaigns. Physical ability to reach high points in equipment, tanks, towers, and use lift/ladder/tools to sample difficult locations. Desire to grow within MS&T, gaining exposure to microbiology, cleaning validation, and lifecycle process support in a regulated pharmaceutical environment. Seniority level : Associate Employment type : Contract Job function : Science, Manufacturing and Engineering Industries : Pharmaceutical Manufacturing, Chemical Manufacturing, and Medical Equipment Manufacturing

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