Quality Checker-1st Shift

NOW HIRING QUALITY INSPECTORS FOR A MEDICAL DEVICE COMPANY!
Shift - 1st Shift

The Quality Inspector supports the organization by reviewing, organizing, and maintaining manufacturing documentation within a regulated medical device environment. This role focuses on scanning and archiving records, ensuring documentation accuracy, and managing a backlog of manufacturing files using a digital document control system. The Quality Inspector works extensively with computer-based tools to verify training records, support quality assurance activities, and help prioritize urgent change orders.

Scan, archive, and organize manufacturing documents within the designated document control system (Master Controls).

Locate and retrieve specific records efficiently to support quality and manufacturing activities.

Review manufacturing records and verify that required training has been completed, including crediting training performed outside of the system when appropriate.

Ensure manufacturing files are organized properly and consistently in accordance with internal procedures and regulatory expectations.

Help identify and prioritize urgent change orders, ensuring that documentation related to these changes is processed and maintained accurately.

Perform detailed document review for accuracy, completeness, and compliance with medical device regulations and internal quality standards.

Strong computer proficiency and ability to work expertly with digital tools and systems.

Experience working in a quality department with responsibility for reviewing documents.

Knowledge of medical device regulations and how they apply to documentation and quality processes.

Experience in quality inspection, quality assurance, and quality control activities.

Experience with document control in a regulated environment.

Familiarity with FDA-related requirements in a medical device context.

Proficiency using Microsoft Teams for collaboration and communication.

Proficiency using Microsoft Outlook for email and calendar management.

Experience working with SharePoint for document management is beneficial.

Familiarity with deviation management and organization of quality records is a plus.

Experience with Master Controls or similar document control systems is helpful.

Interest in learning more about manufacturing documentation organization and quality system processes.

This is a Contract to Hire position based out of San Diego, CA.

If eligible, the benefitsavailable for this temporary role may include the following:

Medical, dental & vision

401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available

Life Insurance (Voluntary Life & AD&&D for the employee and dependents)

Short and long-term disability

Health Spending Account (HSA)

Employee Assistance Program

Application Deadline
Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

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