Staffing Resource Group, Inc
Entry Level Microbiology and Cleaning Validation Associate
Staffing Resource Group, Inc, Florida, New York, United States
Entry Level Microbiology and Cleaning Validation Associate
Posted: 01/09/2026
Employment Type: Contract
Division: Life Sciences
Job Number: JN -012026-20898
State: Florida
Job Description Title:
Microbiology & Cleaning Validation Associate
Pay Rate:
$35.00/hr.
Location:
Davie, FL (local candidates only)
Shift Schedule:
Monday to Friday 8am-5pm
Duration:
Contract up to 9 months with possible extension
Overview 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, 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.
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.
Qualifications
Master’s degree in microbiology, biology, or biotechnology.
Entry‑level experience: 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 understanding of microbiology principles and contamination control, aseptic and low‑bioburden handling practices.
Aware 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.
Personal Attributes
Hands‑on, detail‑oriented, and quality‑focused.
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 of lift/ladder/tools to sample difficult to reach locations.
ADA/EOE
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Job Description Title:
Microbiology & Cleaning Validation Associate
Pay Rate:
$35.00/hr.
Location:
Davie, FL (local candidates only)
Shift Schedule:
Monday to Friday 8am-5pm
Duration:
Contract up to 9 months with possible extension
Overview 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, 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.
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.
Qualifications
Master’s degree in microbiology, biology, or biotechnology.
Entry‑level experience: 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 understanding of microbiology principles and contamination control, aseptic and low‑bioburden handling practices.
Aware 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.
Personal Attributes
Hands‑on, detail‑oriented, and quality‑focused.
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 of lift/ladder/tools to sample difficult to reach locations.
ADA/EOE
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