Integrated Resources, Inc ( IRI )
Integrated Resources, Inc ( IRI ) provided pay range
This range is provided by Integrated Resources, Inc ( IRI ). Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $35.00/hr - $35.00/hr
Recruitment Manager | Driving Pharma & Biotech Hiring Success | Talent Strategy & Leadership. About the Company 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.
About the Role 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.
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, Biotechnology.
Required Skills
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 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.
Preferred Skills
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.
Seniority level Associate
Employment type Contract
Job function Research
Industries Pharmaceutical Manufacturing
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Base pay range $35.00/hr - $35.00/hr
Recruitment Manager | Driving Pharma & Biotech Hiring Success | Talent Strategy & Leadership. About the Company 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.
About the Role 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.
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, Biotechnology.
Required Skills
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 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.
Preferred Skills
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.
Seniority level Associate
Employment type Contract
Job function Research
Industries Pharmaceutical Manufacturing
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