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Quality Technicians

Job in San Jose, Santa Clara County, California, 95112, USA
Listing for: inSync Staffing
Full Time position
Listed on 2026-08-18
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, Production QC/QA, Quality Engineering
Job Description & How to Apply Below

Quality Technician II

Pay $28-30 7am to 3:30pm 3 month+ assignment Experience with medical device inspection. Able to work overtime and possibly on Saturday.

Qualifications
  • 3–5 years of manufacturing experience, preferably in medical device manufacturing.
  • Experience performing quality inspections and following quality procedures.
  • Knowledge of inspection methods, documentation practices, and regulatory requirements.
  • Ability to read and interpret engineering drawings, blueprints, and product specifications.
  • Proficient with Microsoft Office (Word, Excel, Outlook).
  • High school diploma or equivalent required.
  • Willing to work overtime and Saturdays as needed.
Professional Summary

Experienced manufacturing and quality professional with a background in medical device inspection, quality assurance, and manufacturing operations. Skilled in performing inspections, reviewing documentation, identifying quality issues, and ensuring products meet company and regulatory standards. Strong ability to work independently while collaborating with Manufacturing, Engineering, and Quality teams to improve processes and maintain product quality.

Key Responsibilities
  • Perform product inspections, audits, and quality checks to ensure compliance with company procedures and regulatory requirements.
  • Review production records and documentation for accuracy and completeness.
  • Verify products meet engineering drawings, specifications, and quality standards.
  • Identify quality issues and assist with root cause investigations and corrective actions (CAPA).
  • Support equipment, process, and method validation activities.
  • Monitor calibration status of inspection and test equipment.
  • Document inspection results and maintain accurate quality records.
  • Update work instructions, inspection procedures, and quality documentation.
  • Work closely with Manufacturing, Engineering, and Quality Assurance teams to resolve quality concerns and improve processes.
  • Ensure nonconforming products are properly identified, documented, and escalated according to quality procedures.

This version is optimized for resumes and ATS (Applicant Tracking Systems) by emphasizing keywords such as medical device manufacturing, quality inspection, CAPA, SOPs, quality assurance, validation, calibration, engineering drawings, regulatory compliance, and documentation.

Benefits (employee contribution):

  • Health insurance
  • Health savings account
  • Dental insurance
  • Vision insurance
  • Flexible spending accounts
  • Life insurance
  • Retirement plan

All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Rate of pay within the stated range will depend on the qualification of the applicant.

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