MS&T Specialist I

Job Title: MS&T Specialist I
Location: Davie, FL 33314
Duration: 9 Months+ (Possible Extension)
 
Shift Schedule: Monday to Friday, 8:00 AM – 5:00 PM
Temp to Perm: Possibility based on worker performance and openings
 
Core Essential Skill Sets:

• 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

1. Medical Screenings:
   • Vision Screen – Near, Far, Color, Depth, and Peripheral
   • Spirometry & OSHA Respirator Questionnaire
2. Basic Background
3. Drug Screening:
   • 11-panel drug test with Fentanyl

• 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.
• Focuses on sampling execution, data documentation, and on-floor support, risk assessments, investigations, working under the guidance of MS&T scientists and engineers to ensure equipment cleanliness, contamination control, and inspection readiness.

• 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.

• Master’s degree in Microbiology, Biology, or Biotechnology

• 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

• 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
• Ability to reach high points in equipment, tanks, towers and use 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.