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!

-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.

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