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Biotech Cleanroom Jobs in Raleigh, NC (NOW HIRING)

Sterility Assurance Lead

Raleigh, NC · On-site

$90K - $110K/yr

Bachelor's or Master's degree in Microbiology, Pharmaceutical Sciences, Biotechnology, Engineering ... Strong knowledge of microbiology principles, contamination control, and cleanroom manufacturing

Senior Project Manager

Durham, NC · On-site

$108K - $201K/yr

... biotechnology, or other GMP-regulated manufacturing environments. * Proven success managing ... and cleanroom environments. * Demonstrated ability to manage budgets, schedules, risks, change ...

... Cleanroom facilities. Astro Pak provides services to over 15 sectors including: Data Centers, Biotechnology, Pharmaceutical, Aerospace, Semiconductor, and other selected Industrial markets. The ...

... biotechnology, or other GMP-regulated manufacturing environments. * Proven success managing ... and cleanroom environments. * Demonstrated ability to manage budgets, schedules, risks, change ...

Field Technician

Raleigh, NC

$19.25 - $26.25/hr

... Cleanroom facilities. Astro Pak provides services to over 15 sectors including: Data Centers, Biotechnology, Pharmaceutical, Aerospace, Semiconductor, and other selected Industrial markets. The ...

Field Technician

Raleigh, NC · On-site

$19.25 - $26.25/hr

... Cleanroom facilities. Astro Pak provides services to over 15 sectors including: Data Centers, Biotechnology, Pharmaceutical, Aerospace, Semiconductor, and other selected Industrial markets. The ...

... Cleanroom facilities. Astro Pak provides services to over 15 sectors including: Data Centers, Biotechnology, Pharmaceutical, Aerospace, Semiconductor, and other selected Industrial markets. The ...

Showing results 41-60

Biotech Cleanroom information

See Raleigh, NC salary details

$11

$21

$39

How much do biotech cleanroom jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for biotech cleanroom in Raleigh, NC is $21.40, according to ZipRecruiter salary data. Most workers in this role earn between $16.83 and $23.37 per hour, depending on experience, location, and employer.

What is a biotech cleanroom?

A Biotech Cleanroom is a specially designed, controlled environment used in biotechnology labs and manufacturing facilities to minimize contamination from dust, microbes, or other airborne particles. These rooms maintain strict temperature, humidity, and particle count standards to protect sensitive biological samples and processes. Workers in biotech cleanrooms follow rigorous gowning and hygiene protocols, and equipment is regularly sterilized. Cleanrooms are essential in producing pharmaceuticals, medical devices, and other biotech products that require high levels of purity and safety.

What are the key skills and qualifications needed to thrive as a biotech cleanroom technician?

To thrive as a Biotech Cleanroom Technician, you need knowledge of aseptic techniques, good laboratory practices (GLP), and a background in biology or biotechnology, often with an associate’s or bachelor’s degree. Familiarity with cleanroom protocols, environmental monitoring equipment, and compliance systems like GMP (Good Manufacturing Practice) is typically required. Attention to detail, reliability, and effective communication are critical soft skills for maintaining sterile environments and following strict procedures. These skills ensure product safety, regulatory compliance, and consistent quality in sensitive biotech manufacturing processes.

What are some common challenges faced when working in a biotech cleanroom environment?

One of the main challenges in a biotech cleanroom is maintaining strict adherence to contamination control protocols while performing complex tasks. Employees must follow rigorous gowning procedures, regularly sanitize equipment, and be vigilant about minimizing particle generation. The controlled environment can feel restrictive due to specialized attire and limited personal items, but it's essential for ensuring product quality and safety. Teamwork and clear communication are crucial, as tasks often require coordination with colleagues to maintain workflow efficiency and compliance with regulatory standards.

What is the difference between Biotech Cleanroom vs Laboratory Technician?

AspectBiotech CleanroomLaboratory Technician
Required CredentialsCleanroom certification, life sciences trainingAssociate degree or relevant certification, lab safety training
Work EnvironmentControlled cleanroom environment, strict contamination controlStandard laboratory setting, varied equipment
Industry UsageBiotech manufacturing, pharmaceutical productionResearch labs, clinical testing

Biotech Cleanroom specialists focus on maintaining contamination-free environments for biotech and pharmaceutical manufacturing, requiring specialized cleanroom protocols. Laboratory Technicians support research and testing in general lab settings. While both roles require scientific knowledge, cleanroom roles emphasize contamination control and certification, whereas lab technicians focus on testing and data collection.

What are popular job titles related to Biotech Cleanroom jobs in Raleigh, NC?

For Biotech Cleanroom jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Biotech Cleanroom jobs in Raleigh, NC look for?

The top searched job categories for Biotech Cleanroom jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Biotech Cleanroom jobs?

Cities near Raleigh, NC with the most Biotech Cleanroom job openings:

Infographic showing various Biotech Cleanroom job openings in Raleigh, NC as of August 2026, with employment types broken down into 73% Full Time, 7% Part Time, 13% Contract, and 7% Nights. Highlights an 100% In-person job distribution, with an average salary of $44,504 per year, or $21.4 per hour.

Sterility Assurance Lead

Kelly Services

Raleigh, NC • On-site

$90K - $110K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 10 days ago


Job description

The Sterility Assurance Lead is responsible for leading and maintaining site-wide sterility assurance and contamination control programs within a sterile pharmaceutical manufacturing environment. This role provides technical leadership and oversight for terminally sterilized and injectable drug product operations, ensuring compliance with FDA aseptic processing guidance, EU Annex 1, cGMP standards, and global regulatory requirements. The position serves as the site Subject Matter Expert (SME) for sterility assurance, environmental monitoring, microbiological risk management, and contamination control strategies while supporting process validation, regulatory inspections, and continuous improvement initiatives.
Location: Raleigh NC
Salary: $90,000-$110,000/year
Direct Hire role
No relocation assistance offered

Key ResponsibilitiesSterility Assurance & Contamination Control
  • Develop, implement, and maintain sterility assurance and contamination control programs for sterile manufacturing operations
  • Lead the site Contamination Control Strategy (CCS) and ensure alignment with regulatory expectations and industry best practices
  • Serve as SME for sterility assurance, microbiological oversight, and contamination control activities
  • Define and monitor microbiological and particulate alert/action limits
  • Ensure environmental monitoring programs are effectively designed, executed, evaluated, and maintained throughout the product lifecycle
  • Support inspection readiness and participate in regulatory inspections and audits as the sterility assurance SME
  • Prepare and support responses to regulatory observations related to sterility assurance and contamination control
Process Oversight, Validation & Qualification
  • Provide oversight for terminal sterilization and aseptic manufacturing processes across development, validation, and commercial operations
  • Review and approve critical manufacturing and sterilization activities including washing, filling, sterilization cycles, and environmental controls
  • Review and approve validation strategies, protocols, and reports including IQ/OQ/PQ activities
  • Ensure appropriate microbiological and particulate control strategies are established and maintained
  • Support ongoing process verification and continued process monitoring activities
Investigations, Risk Assessment & CAPA
  • Lead or support investigations involving microbiological deviations, contamination events, and sterility-related nonconformances
  • Conduct and review risk assessments related to sterility assurance and contamination control
  • Drive development and implementation of CAPAs to mitigate contamination and sterility risks
  • Monitor trends and recurring issues to identify and address systemic risks
Cross-Functional Collaboration & Training
  • Partner with Manufacturing, Engineering, Validation, Quality Control Microbiology, and Quality Assurance teams to ensure effective sterility assurance integration
  • Provide coaching, training, and guidance on contamination control principles, aseptic behaviors, and sterility assurance best practices
  • Support development and revision of SOPs, work instructions, and training materials
  • Promote a strong quality culture focused on compliance, contamination control, and operational excellence
Continuous Improvement & Operational Support
  • Participate in operational excellence and continuous improvement initiatives
  • Support technology transfers, new product introductions, and cross-functional projects
  • Assist with internal audits, gap assessments, and periodic reviews of sterility assurance systems
  • Support departmental and site objectives as assigned
QualificationsEducation
  • Bachelor’s or Master’s degree in Microbiology, Pharmaceutical Sciences, Biotechnology, Engineering, or related scientific discipline
Experience
  • Minimum 5 years of experience in sterile pharmaceutical manufacturing, injectable products, or terminal sterilization environments
  • Experience supporting aseptic processing and/or terminal sterilization operations
  • Strong knowledge of microbiology principles, contamination control, and cleanroom manufacturing
  • Experience supporting validation, qualification, and regulatory compliance activities

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
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