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Biotech Cleanroom Jobs in Puerto Rico (NOW HIRING)

Techengpr

HVAC Systems Utilities Engineer

Carolina, PR · On-site

$80 - $100/hr

Minimum 5+ years of experience supporting HVAC systems in pharmaceutical, biotechnology, medical device, or regulated manufacturing environments. * Strong knowledge of: * Cleanroom HVAC systems * Air ...

Veg Group

Project Manager

Gurabo, PR · On-site

$90 - $120/hr

... biotechnology, medical device, or other FDA‑regulated industries. * Experience supporting manufacturing, packaging, facilities, utilities, process equipment, cleanroom environments, and regulated ...

Pinnaql

Project Engineer

Gurabo, PR · On-site

... biotechnology, medical device, or other FDA-regulated industries. * Experience supporting manufacturing systems, packaging equipment, facilities, utilities, process equipment, cleanroom environments ...

Veg Group

Project Engineer

Humacao, PR · On-site

$75 - $100/hr

... biotechnology, medical device, or other FDA‑regulated industries. * Experience supporting manufacturing systems, packaging equipment, facilities, utilities, process equipment, cleanroom ...

Pinnaql

Project Engineer

Juncos, PR · On-site

... biotechnology, medical device, or other FDA-regulated industries. * Experience supporting manufacturing systems, packaging equipment, facilities, utilities, process equipment, cleanroom environments ...

Pinnaql

Project Engineer

Humacao, PR · On-site

... biotechnology, medical device, or other FDA-regulated industries. * Experience supporting manufacturing systems, packaging equipment, facilities, utilities, process equipment, cleanroom environments ...

Veg Group

Project Engineer

Gurabo, PR · On-site

$70 - $90/hr

... biotechnology, medical device, or other FDA‑regulated industries. * Experience supporting manufacturing systems, packaging equipment, facilities, utilities, process equipment, cleanroom ...

Pinnaql

Project Engineer

Humacao, PR · On-site

... biotechnology, medical device, or other FDA-regulated industries. * Experience supporting manufacturing systems, packaging equipment, facilities, utilities, process equipment, cleanroom environments ...

Pinnaql

Project Engineer

Punta Santiago, PR · On-site

... biotechnology, medical device, or other FDA-regulated industries. * Experience supporting manufacturing systems, packaging equipment, facilities, utilities, process equipment, cleanroom environments ...

Pinnaql

Project Manager

Gurabo, PR · On-site

... biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing, packaging, facilities, utilities, process equipment, cleanroom environments, and ...

Pinnaql

Project Manager

Humacao, PR · On-site

... biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing, packaging, facilities, utilities, process equipment, cleanroom environments, and ...

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Showing results 1-20

All JobsBiotech Cleanroom JobsBiotech Cleanroom Jobs in Puerto Rico

Biotech Cleanroom information

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 job categories do people searching Biotech Cleanroom jobs in Puerto Rico look for?

The top searched job categories for Biotech Cleanroom jobs in Puerto Rico are:

Biotech Cleanroom jobs near you
Infographic showing various Biotech Cleanroom job openings in Puerto Rico as of August 2026, with employment types broken down into 1% As Needed, 92% Full Time, 3% Part Time, and 4% Contract. Highlights an 80% Physical, 4% Hybrid, and 16% Remote job distribution.

Contamination Control and Sterility Assurance Sr. Specialist

Danaher

Fajardo, PR • On-site

$79K - $109K/yr

Full-time

Medical, Life, PTO

Posted 4 days ago

Danaher rating

7.7

Company rating: 7.7 out of 10

Based on 31 frontline employees who took The Breakroom Quiz

193rd of 546 rated manufacturers

Job description

Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.
You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
The Contamination Control & Sterility Assurance Sr. Specialist (P2) is responsible for driving contamination control strategies, supporting sterility assurance programmes and ensuring compliance with regulatory requirements and internal quality standards.
The role provides technical leadership for contamination control, environmental monitoring, microbiological laboratory testing, cleanroom qualification, and sterility assurance activities to support product quality, Quality and Regulatory compliance across manufacturing and laboratory operations.
This position reports to the Senior Manager, CCSA and is part of the Global CCSA team located in Fajardo site.
Work arrangement to be confirmed as on-site.
What you will do:
  • Develop, implement, and maintain contamination control strategies and sterility assurance programmes in alignment with global regulatory requirements and internal quality standards to support product quality, patient safety, and compliance.
  • Lead and support microbiological lifecycle and qualification activities, including test method management, cleanroom qualification and requalification programmes, protocol execution, technical assessments, deviation management, and report approval.
  • Provide oversight of microbiological and environmental monitoring programmes, including endotoxin, bioburden, sterility, and non-viable particulate monitoring, while analysing and trending data to identify risks and drive continuous improvement.
  • Lead investigations related to contamination events, environmental monitoring excursions, deviations, and out-of-specification results, utilizing root cause analysis and ensuring the implementation of effective corrective and preventive actions (CAPAs).
  • Collaborate with Quality, Operations, Engineering, and other cross-functional teams to conduct GEMBA walks, execute Quality Risk Management activities (including FMEA), support audits and inspections, and advance continuous improvement initiatives.

Who you are:
  • Bachelor's degree in microbiology or a related scientific discipline.
  • Minimum 5 years of relevant experience in contamination control, environmental monitoring, cleanroom management and sterility assurance within pharmaceutical, medical device or biotechnology industries.
  • Proven experience with cleanroom qualification and environmental monitoring programmes.
  • Strong capability in data analysis, environmental monitoring trending and interpretation of microbiological and particulate data.
  • Knowledge of relevant standards, such as ISO 14644, ISO 11137, ISO 11737 and EN 17141, and experience with quality systems including corrective and preventive action, change control and deviation management.
Travel, Motor Vehicle Record & Physical/Environment Requirements:
  • Ability to travel as required to support site's contamination control, sterility assurance, supplier audit or project activities.
It would be a plus if you also possess previous experience in:
  • Experience with endotoxin, bioburden, sterility, and particulate testing programmes.
  • Experience supporting sterilisation validation, dose audits, or sterility assurance programmes.
  • Acting as a subject matter expert during regulatory inspections, customer audits, and internal quality audits.

Work Arrangement
This position is based at Cytiva's Fajardo, Puerto Rico site and is an on-site role. The successful candidate will be expected to work regularly in manufacturing, laboratory, and cleanroom environments and collaborate closely with site and global cross-functional teams.
Benefits
Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.
The U.S. EEO posters are available here.
For candidates who are based outside of New York City or who are applying for roles outside of New York City, for more information about conditions of any job offer please click here.
We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or applyassistance@danaher.com.

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About Danaher

Sourced by ZipRecruiter

We are a science and technology innovator committed to helping our customers solve complex challenges, and improving quality of life around the world. A global family of more than 20 operating companies, we drive meaningful innovation in some of today's most dynamic, growing industries.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Washington, DC, US

Year founded

1984

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