1

Biotech Cleanroom Jobs in Texas (NOW HIRING)

Quality Assurance Specialist IV

Houston, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Bachelor's degree in Biology, Biotechnology, Life Sciences, Engineering, or a related scientific ... Knowledge of aseptic processing, cleanroom operations, and gowning requirements is required.

New

Senior Manufacturing Associate

Houston, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Associate's or Bachelor's degree in a scientific field (e.g., biology, biotechnology, or related ... Demonstrated experience executing aseptic processing and working in cleanroom environments (Grade A ...

Field Technician

Houston, TX · On-site

$18.75 - $25.75/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

Houston, TX · On-site

$18.75 - $25.75/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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

Commercial Strategies Lead - Life Sciences

Houston, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This role supports large, capitalintensive facilities such as pharmaceuticals, biotechnology and ... skids, cleanroom systems, GMPrelated equipment, validated utilities, specialty piping, and ...

Environmental Monitoring Technician will support activities in the cleanroom, laminar flow hoods ... Demonstrated relevant experience in a microbiology laboratory (Q.C., pharmaceutical, biotech or ...

... 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 ...

Project Technician

Beaumont, TX · On-site

$16.50 - $22.50/hr

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

New

Project Technician

Houston, TX · On-site

$16.50 - $22.50/hr

  • Medical

  • Retirement

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

New

Showing results 21-40

Biotech Cleanroom information

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 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 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 popular job titles related to Biotech Cleanroom jobs in Texas? For Biotech Cleanroom jobs in Texas, the most frequently searched job titles are:
What job categories do people searching Biotech Cleanroom jobs in Texas look for? The top searched job categories for Biotech Cleanroom jobs in Texas are:
What cities in Texas are hiring for Biotech Cleanroom jobs? Cities in Texas with the most Biotech Cleanroom job openings:
Infographic showing various Biotech Cleanroom job openings in Texas as of August 2026, with employment types broken down into 84% Full Time, 8% Part Time, and 8% Contract. Highlights an 100% In-person job distribution.

Quality Assurance Specialist IV

Lonza

Houston, TX • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted yesterday

New


Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

25th of 86 rated pharmaceutical


Job description

Quality Assurance Specialist IV
Location: This is an on-site position located in Pearland, TX.
Available shift: 8:00 am to 5:00 pm Monday through Friday.
The Quality Assurance Specialist IV serves as a senior quality representative supporting Cell Therapy manufacturing operations and associated support functions. This role provides Quality Assurance oversight for GMP manufacturing activities, quality systems, investigations, and documentation while ensuring compliance with cGMP regulations and company procedures. The position partners closely with Manufacturing, Quality Control, and Quality Systems teams to support production activities, review and approve quality records, drive issue resolution, and maintain a state of inspection readiness. The role also serves as a key quality resource for internal and external stakeholders while supporting continuous improvement initiatives and product quality objectives.
What you will get:
This is a competitive, salary position. In addition, below you will find a comprehensive summary of the benefits package we offer:
Performance-related bonus.
Medical, dental and vision insurance.
401(k) matching plan.
Life insurance, as well as short-term and long-term disability insurance.
Employee assistance programs.
Paid time off (PTO).
Compensation for this role will be determined by the candidate's qualifications, skills, experience, and relevant knowledge.
What you will do:
Perform Quality Assurance review and approval of GMP documents, including master documents, executed production records, deviations, investigations, CAPAs, change controls, and controlled documents.
Provide QA support and oversight for Cell Therapy manufacturing operations to ensure compliance with cGMP requirements and site procedures.
Conduct QA walkthroughs and on-the-floor quality oversight activities; partner with manufacturing and support groups to identify, investigate, and resolve operational issues.
Support deviation management, CAPA development, investigation activities, and change control processes as either record owner or QA approver.
Review and approve GMP documentation generated by Manufacturing, QC, Material Management, Facilities & Engineering, and other supporting departments.
Perform material release and lot disposition activities in accordance with approved procedures and quality requirements.
Represent Quality Assurance in internal and external client meetings to ensure quality expectations and regulatory requirements are met.
Track and manage quality system records to support timely closure and compliance objectives.
Support internal audits, customer audits, regulatory inspections, and inspection readiness initiatives.
Provide QA support regarding aseptic manufacturing activities, including gowning, cleanroom operations, and aseptic processing requirements as needed.
Collaborate cross-functionally with Manufacturing, QC, and Quality Systems teams to drive compliance, process improvements, and operational excellence.
Perform other duties as assigned.
What we are looking for:
Experience from 5+ years in Quality Assurance within a GMP-regulated biopharmaceutical, cell therapy, or related manufacturing environment.
Bachelor's degree in Biology, Biotechnology, Life Sciences, Engineering, or a related scientific discipline is required.
Experience supporting GMP manufacturing operations is required.
Experience in Cell Therapy manufacturing is strongly preferred.
Demonstrated experience with deviations, investigations, CAPAs, and change controls is required.
Knowledge of aseptic processing, cleanroom operations, and gowning requirements is required.
Experience with TrackWise and electronic quality management systems is preferred.
Strong understanding of cGMP requirements, FDA regulations, quality systems, and compliance expectations.
Experience reviewing and approving GMP documentation and quality records.
Strong technical writing, root cause analysis, risk management, and problem-solving skills.
Ability to work independently, prioritize multiple activities, and make sound quality decisions in a fast-paced manufacturing environment.
Strong communication and collaboration skills with the ability to effectively partner across multiple departments.
Proficiency in Microsoft Office applications and quality-related systems such as Documentum, SAP, and LIMS is preferred.
About Lonza:
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.

What Lonza employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom