Quality Inspector – Pharma/Medical Device QC

AppleOne Employment Services

Camarillo (CA)

On-site

USD 54,000 - 78,000

Full time

14 days+
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Job summary

AppleOne Employment Services invites applications for a Quality Control Inspector in Camarillo, CA. The role involves inspecting materials, components and finished products throughout manufacturing under GMP/regulated environments.

1st shift, 5am–2:30pm with occasional OT; strong attention to detail and ability to work both independently and in teams are essential. Candidates should have 3+ years of QC/inspection experience, familiarity with ISO 9001/13485 and FDA regulations, and experience

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.

Education

High School Diploma
3+ years QC/inspection

Tools

Calipers
Tape measures
Rulers
Pin gauges
ERP system
GMP SOPs

Job description

AppleOne Employment Services invites applications for a Quality Control Inspector in Camarillo, CA. The role involves inspecting materials, components and finished products throughout manufacturing under GMP/regulated environments.

1st shift, 5am–2:30pm with occasional OT; strong attention to detail and ability to work both independently and in teams are essential. Candidates should have 3+ years of QC/inspection experience, familiarity with ISO 9001/13485 and FDA regulations, and experience

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