Microbiologist Job at Integrated Resources, Inc ( IRI ), Davie, FL

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  • Integrated Resources, Inc ( IRI )
  • Davie, FL

Job Description

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.

Job Tags

Internship, Shift work, Weekend work,

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