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Quality Control Inspector

Job in Ventura, Ventura County, California, 93006, USA
Listing for: Jobot
Full Time position
Listed on 2026-03-08
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control / Manager, Quality Technician/ Inspector
  • Manufacturing / Production
Salary/Wage Range or Industry Benchmark: 25 USD Hourly USD 25.00 HOUR
Job Description & How to Apply Below

Job details:
Salary: $25 - $25 per hour.

Hosted by:
Mathew Fallon.

Are you a fit? Easy Apply now by clicking the "Easy Apply" button and submitting your resume.

About us

A top Medical Device Manufacturer in Southern California focused on engineering and manufacturing of high‑quality medical devices.

Benefits
  • 401(k)
  • 401(k) matching
  • Dental insurance
  • Health insurance
  • Life insurance
  • Paid time off
  • Parental leave
  • Vision insurance
Responsibilities
  • Conduct regular inspections and audits of the production process to ensure adherence to quality standards and regulatory requirements.
  • Identify any issues or deviations in quality and report them promptly to the management team.
  • Collaborate with production and operations teams to implement corrective actions and quality improvement strategies.
  • Maintain detailed records of inspection results, documenting any issues and the steps taken to resolve them.
  • Ensure that all products meet company specifications and customer expectations.
  • Perform regular reviews of quality control processes and make recommendations for continuous improvement.
  • Assist in the development and implementation of quality control training programs for staff.
  • Collaborate with management to establish quality benchmarks and standards for each product.
  • Stay updated on industry trends and emerging technology that could enhance quality control efforts.
Qualifications
  • High School Diploma or equivalent is required.
  • A minimum of 5 years’ experience in a quality control or quality assurance role.
  • Proficient in basic computer skills, including data entry and report generation.
  • Comprehensive understanding of FDA and ISO 13485 regulations.
  • Solid knowledge of Good Manufacturing Practices (GMP).
  • Familiarity with quality and inventory systems, with the ability to quickly learn new software and technologies.
  • Strong attention to detail, with the ability to identify small discrepancies or errors.
  • Excellent problem‑solving skills and the ability to develop effective solutions to quality issues.
  • Strong communication skills, with the ability to clearly and effectively convey complex information to a variety of audiences.
  • Ability to work independently and as part of a team, managing multiple tasks and projects simultaneously.
  • Ability to stand for extended periods and lift up to 50 lbs.

Join our team and play a pivotal role in maintaining the quality that our customers have come to expect. Apply today and start making a difference!

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