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# Quality Assurance Technician

- **Company:** Talnt LLC
- **Location:** Woodland, CA, United States
- **Experience:** Starter
- **Salary:** $52,000.0 - $62,400.0
- **Contract:** Permanent contract
- **Skills:** Document Management Systems, Microsoft Office, Pareto Chart, Performance Monitor
- **Published:** May 31, 2026
- **Apply:** https://www.indeed.com/viewjob?jk=f44a5de8437df9aa

## About the Role

Do you have experience in Customer complaint resolution?, Do you have a Bachelor's degree?, * Bachelor's degree in a related field preferred, or 1-2 years of experience in a regulated manufacturing environment.

 * Working knowledge of ISO 13485 and FDA 21 CFR Part 820 Quality System Regulations.
 * Familiarity with cGMP and medical device compliance requirements.
 * Experience supporting CAPA, NCR, change control, or complaint investigations preferred.
 * Ability to read and interpret technical drawings and regulatory documents.
 * Strong analytical and problem-solving skills.
 * Proficiency in Microsoft Office applications.
 * Experience with quality tools and documentation systems preferred.
 * Strong written and verbal communication skills.

Physical & Work Environment

 * In-person role within a regulated manufacturing facility.
 * Ability to support production floor activities and inspection processes.

## Description

The Quality Assurance Technician supports and maintains quality system processes within a regulated medical device manufacturing environment. This role ensures compliance with ISO 13485, FDA 21 CFR Part 820, cGMP, and applicable regulatory standards while supporting production quality activities across incoming, in-process, and final release stages.

The ideal candidate is detail-oriented, knowledgeable in medical device quality systems, and capable of supporting audits, documentation control, investigations, and quality improvement initiatives in a fast-paced production environment., * Coordinate and support quality system processes including:

 + Nonconforming Material Reports (NCR)
 + Corrective and Preventive Actions (CAPA)
 + Complaint Handling
 + Change Control
 + Validation Programs
 + Supplier Qualification and Monitoring
 + Calibration Program
 + Internal Audit Program
 * Perform QA Final Release activities for incoming inspection, in-process inspection, and finished goods review.
 * Interpret engineering drawings, specifications, and regulatory requirements.
 * Assist with internal audits and support external audits including customer and third-party audits.
 * Track and implement corrective actions resulting from audit findings.
 * Ensure compliance with FDA, cGMP, ISO 13485, and medical device regulatory requirements.
 * Maintain documentation and support quality records in accordance with regulatory standards.
 * Utilize quality tools such as root cause analysis, Pareto charts, histograms, and flow diagrams.
 * Support supplier quality initiatives and performance monitoring.
 * Manage departmental inventories using purchase requisitions and material transfers.
 * Collaborate cross-functionally with manufacturing, engineering, and operations teams.
 * Provide training support and foster a quality-focused team environment.


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