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Inspector , Quality Control; Delivery System; Temp

Job in Irvine, Orange County, California, 92713, USA
Listing for: Jenavalve Technology
Seasonal/Temporary position
Listed on 2026-09-12
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, Production QC/QA, Quality Engineering
Salary/Wage Range or Industry Benchmark: 24.2 USD Hourly USD 24.20 HOUR
Job Description & How to Apply Below

Job Details

Job Location:

Irvine, CA 92618

Position Type:
Contractor

Education Level: High School

Salary Range: $24.20 - $24.20 Hourly

Job Title:

Inspector, Quality Control (Delivery System)

Roles:
Inspector I, Quality Control (DS);
Inspector II, Quality Control (DS);
Inspector III, Quality Control (DS)

Role Level: Individual Contributor

Supervisor/Manager

Title:

Senior Manager, Quality Engineering

Job Location & Environment:
Irvine, CA
- Corporate Office/Controlled Clean Room Environment

Job Description Summary

Manufacturing
- Hourly. Responsible for performing quality control inspections, testing, and release activities for Delivery System (DS). Support in-process and final inspections, perform Device History Record (DHR) review and product release to Finished Goods Inventory. Identify issues and non-conformance and collaborate with Quality Engineers on NCR initiation, investigation, and follow-up actions.

Job Responsibilities
  • Perform in-process and final quality inspections of Delivery System subassemblies and finished products, including visual inspection, dimensional verification, and functional testing per approved work instructions, SOPs, and quality procedures.
  • Review Device History Records (DHR) for completeness, accuracy, and conformance to acceptance criteria, ensuring compliance with Good Documentation Practices (GDP/GMP).
  • Conduct inspection of device labeling, including UDI human-readable content and barcode verification.
  • Release DS products to Finished Goods Inventory (FGI) upon successful completion of all quality requirements.
  • Identify quality issues or process deviations during inspection activities and initiate Non-Conformance Reports (NCRs); assist with material containment, root cause investigations, and corrective actions.
  • Support raw material inspection and material release to inventory as needed.
  • Support engineering and quality teams in process validations.
  • Participate in continuous improvement initiatives and provide practical feedback.
  • Maintain line clearance and organize workstations in accordance with cleanroom and company procedures.
  • Complete required training and maintain qualification for assigned inspection processes.
  • Adhere to company policies, quality system requirements, and safety procedures.
  • Maintain reliable and consistent attendance to support production operations, including punctual arrival and the ability to work full scheduled shifts and overtime as required to meet operational and production needs.
  • Other duties as assigned by management.
Qualifications
  • High school diploma or equivalent required. Candidates without a diploma may demonstrate equivalent competency through a validated external assessment.
  • Minimum 1 year of experience in Quality Control or equivalent Manufacturing Inspection within the medical device industry or other regulated precision manufacturing environments.
  • Basic knowledge of quality systems, GDP/GMP, and inspection techniques.
  • Ability to follow detailed work instructions and maintain accurate documentation.
  • The level of this role (Technician I, II, or III) will be determined based on the candidate’s experience, technical skills, and demonstrated competencies relevant to the position.
Skills and Abilities
  • Adhere to company code of conduct and contribute to fostering a professional, collaborative and respectful team working environment.
  • Work effectively in a regulated manufacturing / cleanroom environment.
  • Show strong attention to detail while performing visual and functional inspections.
  • Follow written procedures, work instructions, and quality standards.
  • Good communication skills (verbal and written) and ability to work collaboratively with cross‑functional teams.
  • Learn and apply inspection techniques and tools.
  • Basic understanding of GMP documentation practices.
  • Read, comprehend and speak English.
  • Basic computer skills (MS Office and documentation systems).
Physical Requirements
  • Requires prolonged periods of standing and sitting to support inspection, testing, and review activities.
  • Work in a controlled cleanroom environment while wearing full cleanroom gowning including gown/coveralls, gloves, mask, hairnet, boot covers, and other PPE as needed.
  • Follow clean rooms, laboratory, and site safety protocols at all times.
  • Use inspection and testing equipment as part of routine job duties.
  • Push, pull, twist, climb, balance, stoop, kneel, and crawl as required.
  • Perform repetitive motions such as reaching and grasping.
  • Lift or move materials up to 25 pounds.
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