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Contamination Control Engineer Jobs in Florida (NOW HIRING)

... engineers to ensure equipment cleanliness, contamination control, and inspection readiness. Key Responsibilities * Perform microbiological and cleaning validation sampling, including swab and rinse ...

Trend and interpret microbiological data to support contamination control and sterility assurance ... Collaborate closely with Quality, Manufacturing, Engineering, and Validation teams to support ...

Principal Electrical Engineer

Cape Canaveral, FL ยท On-site

$117K - $144K/yr

Mentor junior engineers and contribute to continual process improvement. * Generate requirements ... Knowledge of satellite/spacecraft system reliability, contamination control, EMI, space ...

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Contamination Control Engineer information

See Florida salary details

$41.1K

$72.2K

$97.9K

How much do contamination control engineer jobs pay per year?

As of Aug 15, 2026, the average yearly pay for contamination control engineer in Florida is $72,169.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,400.00 and $80,700.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a contamination control engineer?

A successful Contamination Control Engineer typically holds a degree in engineering or a related scientific field and possesses expertise in contamination control protocols, cleanroom practices, and environmental monitoring. Familiarity with relevant standards (such as ISO 14644), particulate and microbial detection systems, and certification in contamination control or cleanroom operations are often essential. Excellent attention to detail, problem-solving abilities, and strong communication skills help these engineers implement rigorous protocols and collaborate with multidisciplinary teams. These competencies are crucial to ensuring compliance with regulatory requirements, maintaining product quality, and protecting critical manufacturing or laboratory environments from contamination risks.

What is a contamination control engineer?

A Contamination Control Engineer is responsible for identifying, mitigating, and preventing contamination in controlled environments such as cleanrooms, manufacturing facilities, and laboratories. They develop and enforce protocols to control particles, microbes, and other contaminants that could impact product quality and safety. Their role often involves collaborating with cross-functional teams to ensure compliance with industry regulations and standards. Additionally, they conduct risk assessments, implement contamination control strategies, and oversee facility cleanliness to maintain optimal working conditions.

What are the typical challenges faced by contamination control engineers in the workplace?

Contamination Control Engineers often encounter the challenge of identifying and mitigating sources of particulate and microbial contamination in highly regulated environments such as pharmaceutical, semiconductor, or aerospace facilities. They must stay updated with evolving industry standards and continuously optimize processes despite changes in production or facility design. Collaboration with quality assurance, production, and facilities teams is routine, requiring strong communication to implement preventive measures effectively. These challenges can be rewarding, as overcoming them is essential to ensuring product quality, regulatory compliance, and a safe working environment.

What are popular job titles related to Contamination Control Engineer jobs in Florida?

For Contamination Control Engineer jobs in Florida, the most frequently searched job titles are:

What cities in Florida are hiring for Contamination Control Engineer jobs?

Cities in Florida with the most Contamination Control Engineer job openings:

Infographic showing various Contamination Control Engineer job openings in Florida as of August 2026, with employment types broken down into 58% Full Time, and 42% Contract. Highlights an 60% In-person, and 40% Remote job distribution, with an average salary of $72,169 per year, or $34.7 per hour.

MS&T Specialist I

Unicon Pharma Inc.

Davie, FL โ€ข On-site

Contractor

Re-posted 9 days ago


Job description

Job Title: MS&T Specialist I
Shift Schedule: Monday to Friday 8 am – 5 pm
Temp to Perm role: Possibility based on workers performance and openings
Duration: 9 months with possible extension

Core essential skill sets candidates must have to be considered for the role:

  • 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.

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.

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:

o Microbiology principles and contamination control

o Aseptic and low-bioburden handling practices

  • Awareness of:

o Swab and rinse sampling techniques including environmental monitoring

o TOC (Total Organic Carbon) principles and applications in cleaning verification

o 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
  • 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.