Cleanroom Inspector $24/hr

AppleOne Employment Services; Camarillo (CA); On-site; USD 66,125,000 - 77,146,000; Full time

Benefits offered by this job

Direct hire

Overtime opportunities

Job summary

AppleOne Employment Services in Camarillo, CA is seeking experienced Cleanroom Inspectors and Quality Control Inspectors to join a medical device manufacturing team. This direct-hire role emphasizes accuracy, GMP documentation, and adherence to cleanroom protocols in a regulated production setting.

The position requires 3+ years in quality control inspection, use of calipers/gauges, and strong attention to detail.

Qualifications

• High School Diploma or equivalent.
• Minimum 3 years of quality control inspection or related inspection experience.
• Experience using calipers, gauges, rulers, and other inspection tools.
• Knowledge of GMP practices and quality documentation.
• Experience in a cleanroom environment and wearing PPE.

Responsibilities

• Inspect incoming materials, in-process products, assemblies, components, and finished goods for quality and compliance.
• Perform visual inspections, measurements, and quality checks using documented procedures and tools.
• Review production paperwork, work instructions, inspection records, and quality documentation for accuracy.
• Document inspection findings and quality concerns per GMP and internal standards.
• Support nonconformance reporting, investigations, corrective actions, and improvements.
• Work in a cleanroom environment following gowning, PPE, GMP, and quality system requirements.

Skills

Quality inspection

GMP documentation

Measuring tools

Cleanroom experience

Attention to detail

Education

High School Diploma or equivalent

Tools

Calipers

Gauges

Rulers

Job description

Job Summary

A growing medical device manufacturing team in Camarillo, CA is hiring experienced Cleanroom Inspectors and Quality Control Inspectors for direct hire opportunities. This role is ideal for detail-oriented professionals with experience in medical device assembly inspection, cleanroom manufacturing, GMP documentation, and regulated production environments.

As a Cleanroom Inspector, you will help ensure medical device assemblies, components, materials, and production documentation meet strict quality and compliance standards. This is a great opportunity to join a quality-focused workplace with supportive leadership, clear procedures, strong teamwork, and a culture built around accuracy, accountability, and doing things the right way.

Candidates who take pride in precision, enjoy working in structured manufacturing environments, and want to contribute to products used in healthcare and life sciences will be well-positioned for success.

Key Responsibilities

• Inspect incoming materials, in-process products, medical device assemblies, components, and finished goods for quality and compliance.
• Perform visual inspections, measurements, and quality checks using documented procedures and inspection tools.
• Review manufacturing paperwork, work instructions, inspection records, and quality documentation for accuracy and completeness.
• Document inspection findings, quality concerns, and inspection results in accordance with GMP and internal quality standards.
• Support nonconformance reporting, quality investigations, corrective actions, and continuous improvement activities.
• Work in a cleanroom environment while following gowning, PPE, GMP, and quality system requirements.

Compensation and Benefits

• Direct hire opportunity.
• 1st Shift: $24.00 per hour.
• Start times between 5:30 AM and 6:00 AM.
• Overtime opportunities available.
• Multiple openings available.
• Immediate interviews for qualified candidates.

Required Qualifications and Skills

• Inspect medical device assemblies, components, materials, work-in-process products, and finished goods.
• Perform incoming, in-process, and final inspections in a regulated manufacturing environment.
• Review production documentation, work instructions, inspection records, and quality paperwork.
• Support nonconformance reporting, corrective actions, and quality improvement activities.
• High School Diploma or equivalent required.
• Minimum 3 years of quality control inspection, manufacturing inspection, or related inspection experience required.
• Experience using calipers, gauges, rulers, and other inspection or measurement tools required.
• Knowledge of GMP practices and quality documentation required.
• Comfortable working in a cleanroom environment.
• Experience wearing PPE, including gowning, gloves, masks, and eye protection.
• Strong attention to detail and ability to follow written procedures accurately.
• Strong documentation, communication, organizational, and computer skills.
• Must be legally eligible to work in the United States.
• Experience in medical device, pharmaceutical, biotech, life sciences, or other regulated manufacturing environments.
• Familiarity with nonconformance reporting, quality investigations, and corrective action processes.
• Experience working in a quality-focused production, cleanroom, or operations environment.
• Medical device assembly inspection experience.

Equal Opportunity Employer / Disabled / Protected Veterans

The Know Your Rights poster is available here: https://www.eeoc.gov/sites/default/files/2023-06/22-088_EEOC_KnowYourRights6.12.pdf

The pay transparency policy is available here: https://www.dol.gov/sites/dolgov/files/ofccp/pdf/pay-transp_%20English_formattedESQA508c.pdf

For temporary assignments lasting 13 weeks or longer, AppleOne is pleased to offer major medical, dental, vision, 401k and any statutory sick pay where required.

We are committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation for any part of the employment process, please contact your staffing representative who will reach out to our HR team.

AppleOne participates in the E-Verify program in certain locations as required by law. Learn more about the E-Verify program. https://e-verify.uscis.gov/web/media/resourcesContents/E-Verify_Participation_Poster_ES.pdf

We also consider for employment qualified applicants regardless of criminal histories, consistent with legal requirements, including, if applicable, the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance. Pursuant to applicable state and municipal Fair Chance Laws and Ordinances, we will consider for employment-qualified applicants with arrest and conviction records, including, if applicable, the San Francisco Fair Chance Ordinance. For Los Angeles, CA applicants: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.