eTeam
Get AI-powered advice on this job and more exclusive features.
This range is provided by eTeam. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $34.00/hr - $35.00/hr
Job Title Microbiology & Cleaning Validation Associate
Location Davie, FL 33314
Duration 09 months
Pay Range $(34.00 - 35.00)/hr on W2 all-inclusive without benefits
Shift Schedule Monday to Friday 8am - 5pm
Core essential skill sets candidates must have to be considered for the role
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, 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
Education:
Master’s degree in Microbiology, Biology, Biotechnology.
Experience:
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.
Technical Knowledge & Skills:
Foundational understanding of microbiology principles and 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.
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.
This role involves physical need to reach high points in equipment, tanks, towers and use of lift / ladder / tools to sample difficult to reach locations.
This role offers an excellent entry point into MS&T, providing exposure to microbiology, cleaning validation, and lifecycle process support in a regulated pharmaceutical environment.
Seniority level
Associate
Employment type
Contract
Job function
Research and Science
Industries
Biotechnology Research, Medical Equipment Manufacturing, and Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at eTeam by 2x
Get notified about new Microbiology Specialist jobs in Davie, FL.
#J-18808-Ljbffr
This range is provided by eTeam. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $34.00/hr - $35.00/hr
Job Title Microbiology & Cleaning Validation Associate
Location Davie, FL 33314
Duration 09 months
Pay Range $(34.00 - 35.00)/hr on W2 all-inclusive without benefits
Shift Schedule Monday to Friday 8am - 5pm
Core essential skill sets candidates must have to be considered for the role
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, 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
Education:
Master’s degree in Microbiology, Biology, Biotechnology.
Experience:
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.
Technical Knowledge & Skills:
Foundational understanding of microbiology principles and 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.
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.
This role involves physical need to reach high points in equipment, tanks, towers and use of lift / ladder / tools to sample difficult to reach locations.
This role offers an excellent entry point into MS&T, providing exposure to microbiology, cleaning validation, and lifecycle process support in a regulated pharmaceutical environment.
Seniority level
Associate
Employment type
Contract
Job function
Research and Science
Industries
Biotechnology Research, Medical Equipment Manufacturing, and Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at eTeam by 2x
Get notified about new Microbiology Specialist jobs in Davie, FL.
#J-18808-Ljbffr