Description
Now Hiring: Quality Control Inspector – Medical Device Manufacturing
Location: Irvine, CA | Pay: $28–$32/hour (DOE)
Schedule: Monday–Friday, 8:00 AM – 5:00 PM
Employment Type: Full-time, long-term with potential for growth
Benefits: Comprehensive package including medical, dental, vision, 401(k), and paid time off Join the Team Behind Life-Changing Innovation at Johnson & Johnson
Kelly Services is proud to partner with Johnson & Johnson, a global leader in cardiac arrhythmia treatment and innovation. Johnson & Johnson develops advanced diagnostic and therapeutic catheter-based technologies that help physicians around the world restore patients' heart rhythms and improve quality of life.
We are seeking a Quality Inspector to support the manufacturing and development of these life-saving medical devices at their Irvine, CA facility. Position Overview
As a Quality Inspector, you will play a vital role in ensuring compliance, precision, and product integrity throughout the manufacturing process. You will work hands-on within a cleanroom environment, reviewing Device History Records (DHRs), inspecting production steps, and verifying documentation to meet FDA and ISO standards. Your contribution directly impacts the safety and performance of critical devices used in electrophysiological procedures worldwide. Key Responsibilities
- Inspect in-process and final manufacturing operations and verify compliance with Good Documentation Practices (GDP).
- Review and confirm the accuracy of Device History Records (DHRs) and related documentation.
- Ensure manufacturing processes align with FDA GMP and ISO 13485 standards and company SOPs.
- Collaborate with quality and production teams to support process improvements, validation efforts, and product testing.
- Accurately organize, review, and file quality data records.
- Work effectively in both team-oriented and independent settings to manage tasks and shifting priorities.
- Operate within a cleanroom environment, using appropriate inspection tools and quality protocols.
- Participate in additional quality-related duties as assigned.
- High school diploma or equivalent required; additional technical or quality-related training is a plus.
- Minimum of 1 year of quality inspection experience, preferably within the medical device industry or other regulated environments.
- Familiarity with MS Office tools (Excel, Outlook, Word).
- Ability to read and interpret manufacturing instructions, SOPs, and technical specifications.
- Strong attention to detail, documentation accuracy, and compliance mindset.
- Work with a global medical innovator saving lives through cutting-edge technology.
- Gain experience in FDA-regulated and ISO-certified environments.
- Opportunity for long-term growth and advancement within Johnson & Johnson's world-class operations.
- Competitive pay, full benefits, and a collaborative, mission-driven culture.
Qualified candidates are encouraged to submit an up-to-date resume for immediate consideration. Join us in delivering technology that restores rhythm and changes lives.
Thank you,
Kelly Services – Talent Solutions Partner
kellyservices.com
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