Job ID: 1803210
Reference Code: VV-Quality-Inspector (medical mfg.)
Quality Control Inspector
-Department: Quality Control
-Industry: Pharmaceutical / Medical Device Manufacturing
-Shift: 1st shift, 5am-2:30pm with some OT
-Location: Camarillo, CA
-Job Summary
We are seeking an experienced Quality Control Inspector to inspect materials, components, and finished products throughout the manufacturing process. This position will perform incoming, first article, in-process, and final inspections to ensure products meet company quality standards and applicable regulatory requirements.
The ideal candidate is detail-oriented, quality-driven, and experienced working in a regulated pharmaceutical or medical device manufacturing environment.
-Qualifications
• High School Diploma or equivalent.
• Minimum 3 years of Quality Control/Inspection experience.
• At least 1 year of experience in a pharmaceutical, medical device, or other regulated manufacturing environment preferred.
• Knowledge of GMP, SOPs, and Good Documentation Practices.
• Familiarity with ISO 9001 and/or ISO 13485 preferred.
• Knowledge of FDA regulations, including 21 CFR Parts 210/211 and/or Part 820, preferred.
• Experience with quality inspections, nonconformance reporting, and corrective actions.
• Ability to use measuring tools such as calipers, tape measures, rulers, and pin gauges.
• Good math and computer skills.
• Experience with an ERP system.
• Strong organizational and communication skills.
• Excellent attention to detail and commitment to quality.
• Ability to work independently as well as effectively within a team environment.
***Please send contact and send resume to Veronica Vasquez-Gomez at AppleOne Ventura. Thank you!
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.
Key Responsibilities
• Perform incoming, first article, in-process, and final product inspections.
• Inspect and test materials and products to ensure compliance with quality standards.
• Identify and document non-conforming materials and initiate Nonconformance Reports (NCRs).
• Review and release job order documentation.
• Approve or reject raw materials based on established quality requirements.
• Support investigations related to non-conformances and quality findings.
• Ensure inspections, testing, and documentation are completed accurately and on time.
• Perform pre- and post-inspections associated with the gamma irradiation process.
• Record inspection results, observations, and recommendations.
• Prepare quality metrics and reports for the QC Supervisor or Lead.
• Support continuous improvement and process improvement initiatives.
• Follow all safety procedures and quality requirements.
• Work in an ISO-controlled environment while following appropriate PPE requirements.
• Perform other duties as assigned.