ZipRecruiter

Log In

1

Cleanroom Engineer Jobs in California (NOW HIRING)

Capstan Medical, Inc.

Quality Engineer

Santa Cruz, CA · On-site

$83K - $107K/yr

The Product Quality Engineer is responsible for providing quality engineering support to the ... Oversee product quality during all stages of production in a cleanroom manufacturing environment.

H-Square Corp

Be Seen First

Mechanical Engineer I

Santa Clara, CA · On-site

... in cleanroom facilities throughout the world. At H-Square, our philosophy has always been to ... Create, update, and maintain Engineering Change (EC) documentation and libraries. * Collaborate ...

H-Square Corp

Be Seen First

Mechanical Engineer I

Santa Clara, CA · On-site

... in cleanroom facilities throughout the world. At H-Square, our philosophy has always been to ... Create, update, and maintain Engineering Change (EC) documentation and libraries. * Collaborate ...

Teledyne

Process Integration Engineer

Camarillo, CA

$141K - $189K/yr

This position requires working together with the wafer processing team in the cleanroom to sustain ... Collaboration with cross-functional engineering team to solve material growth and processing issues ...

Teledyne FLIR LLC

Process Integration Engineer

Camarillo, CA · On-site

$141K - $189K/yr

This position requires working together with the wafer processing team in the cleanroom to sustain ... Collaboration with cross-functional engineering team to solve material growth and processing issues ...

JenaValve

Engineer I, Quality (THV)

Irvine, CA · On-site

$81K/yr

Irvine, CA- Corporate office / Controlled Cleanroom Environment Summary: * Provide regular Quality Engineering support to transcatheter Heart Valve (THV) manufacturing and relevant areas including ...

Acara Solutions

Lab Service Engineer

Fremont, CA

$32.29/hr

Job Title: Lab Service Engineer Location: Fremont, CA Employment Type: Contract Industry ... Work Environment: 100% onsite laboratory and cleanroom environment. * Personal Protective Equipment:

INOVIO PHARMACEUTICALS INC

Quality Engineer I

San Diego, CA · On-site

$39.42 - $45.67/hr

Provide quality engineering support and guidance for cleanroom environmental operations to ensure compliance with applicable requirements. * Document, manage, and drive investigations and resolutions ...

INOVIO PHARMACEUTICALS INC

Quality Engineer I

San Diego, CA · On-site

$39.42 - $45.67/hr

Provide quality engineering support and guidance for cleanroom environmental operations to ensure compliance with applicable requirements. * Document, manage, and drive investigations and resolutions ...

Bosch Group

Associate Equipment Engineer

Roseville, CA · On-site

$80K - $90K/yr

An Associate Equipment Engineer is an individual contributor responsible for applying knowledge of ... Researches and adheres to all safety and cleanroom policies. * Train maintenance technicians as ...

previous page

Showing results 41-60

All JobsCleanroom Engineer JobsCleanroom Engineer Jobs in California

Cleanroom Engineer information

See California salary details

$38.5K

$100.4K

$135.7K

How much do cleanroom engineer jobs pay per year?

As of Aug 7, 2026, the average yearly pay for cleanroom engineer in California is $100,420.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,900.00 and $115,000.00 per year, depending on experience, location, and employer.

What is the difference between Cleanroom Engineer vs Quality Control Technician?

AspectCleanroom EngineerQuality Control Technician
CertificationsISO 14644, cleanroom safetyISO 9001, inspection certifications
Work EnvironmentCleanroom facilities, controlled environmentsManufacturing or lab settings, inspection areas
Industry UsagePharmaceuticals, biotech, electronicsPharmaceuticals, manufacturing, biotech

Both roles often require knowledge of industry standards and work in controlled environments. While Cleanroom Engineers focus on designing, maintaining, and ensuring cleanroom conditions, Quality Control Technicians primarily perform inspections and testing to ensure product quality. The roles complement each other in maintaining high standards in regulated industries.

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

To thrive as a Cleanroom Engineer, you need a solid background in engineering or applied sciences, with expertise in contamination control and cleanroom standards such as ISO 14644. Familiarity with monitoring systems, HEPA/ULPA filtration, and cleanroom certification protocols is typically required, along with relevant certifications like IEST or similar. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for ensuring procedures are followed and issues are resolved quickly. These skills and qualities are vital for maintaining stringent environmental standards, ensuring product quality, and supporting regulatory compliance in critical manufacturing environments.

What are some common challenges cleanroom engineers face in maintaining contamination control standards?

Cleanroom Engineers often encounter challenges such as managing airborne particle contamination, ensuring all personnel adhere to strict gowning and entry protocols, and maintaining precise environmental conditions like temperature and humidity. They must also regularly validate and calibrate equipment, troubleshoot HVAC or filtration system issues, and coordinate with production teams to minimize disruptions during maintenance or upgrades. Effective communication and proactive problem-solving are essential to uphold compliance and ensure product quality in this controlled environment.

What is a cleanroom engineer?

Cleanroom Engineers are professionals who design, maintain, and monitor cleanroom environments, which are controlled spaces used in industries such as pharmaceuticals, biotechnology, and electronics manufacturing. Their responsibilities include ensuring that the cleanroom meets strict standards for air quality, temperature, humidity, and particle control. They also troubleshoot equipment, implement contamination control protocols, and ensure compliance with industry regulations. Cleanroom Engineers play a key role in maintaining product quality and safety by minimizing contamination risks.
What are popular job titles related to Cleanroom Engineer jobs in California? For Cleanroom Engineer jobs in California, the most frequently searched job titles are:
What job categories do people searching Cleanroom Engineer jobs in California look for? The top searched job categories for Cleanroom Engineer jobs in California are:
Cleanroom Engineer jobs near you
Infographic showing various Cleanroom Engineer job openings in California as of August 2026, with employment types broken down into 92% Full Time, 2% Part Time, and 6% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $100,420 per year, or $48.3 per hour.

Quality Engineer

Capstan Medical, Inc.

Santa Cruz, CA • On-site

$83K - $107K/yr

Full-time

Re-posted 19 days ago

Job description

The Product Quality Engineer is responsible for providing quality engineering support to the manufacturing line and supporting finished goods release for structural heart implant, delivery, and robotic devices.
Product and Operations Quality responsibilities include:
  • Collaborate with R&D and Regulatory Affairs teams to ensure that biocompatibility requirements are met for medical devices.
  • Provide guidance on sterilization processes and validations to ensure product safety and compliance.
  • Facilitate sterilization activities including batch release, sterilization validation, and coordination with third party sterilizers.
  • Oversee packaging validation activities to ensure product integrity and stability during storage and transportation.
  • Participate in finished goods release processes, ensuring compliance with release criteria and applicable regulatory requirements.
  • Oversee product quality during all stages of production in a cleanroom manufacturing environment.
  • Lead and support investigations into nonconforming materials and products (NCRs), working closely with cross-functional teams including Manufacturing and Engineering, identifying root causes, ensuring timely resolution, and implementing effective corrective and preventive actions (CAPAs) to prevent recurrence.
  • Participate in materials decision making as a member of Material Review Board
  • Collaborate with cross-functional teams, including Manufacturing and Engineering, to resolve quality issues and identify opportunities for process improvement and efficiency gains within the manufacturing environment.
  • Perform audits of manufacturing processes, including inspections, testing, and documentation, to identify areas for improvement and ensure adherence to quality standards.

Documentation and Compliance responsibilities include:
  • Maintain accurate and up-to-date documentation related to quality control processes, inspection results, metrology records, nonconformance reports, and corrective actions.
  • Ensure compliance with relevant regulatory requirements, such as FDA QSR and ISO 13485 standards.
  • Support internal and external audits, including preparation of documentation, participation in audits, and implementation of audit findings.

Skills:
  • Strong understanding of quality management systems.
  • Excellent problem-solving skills and ability to apply root cause analysis methodologies.
  • Detail-oriented with effective organizational and documentation skills.
  • Strong communication and collaboration skills to work cross-functionally and interact with technicians, engineers, auditors, and third parties.
  • Attention to detail, with a focus on accuracy and precision in quality-related activities.
  • Ability to work independently in a fast-paced organization with competing priorities.

Requirements:
  • Bachelor's degree in Engineering or a related technical field. Master's degree is a plus.
  • Knowledge of FDA regulations, ISO 13485, and other relevant quality standards for medical devices.
  • Experience working in a cleanroom manufacturing environment.
  • Experience with nonconforming material investigations and implementing effective CAPAs.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Apply