QC Inspector II 3rd Shift

Insight Global; Irvine (CA); On-site; USD 34,000 - 44,000; Full time

Job summary

Insight Global in Irvine, CA seeks a Quality Control Inspector for a medical device client. You will perform in-line inspections of assemblies and finished products to ensure compliance with quality standards and regulatory requirements.

This 3rd shift role is scheduled Friday, Saturday and Sunday, 5:00 am to 5:30 pm. The ideal candidate works independently, makes sound quality decisions, and maintains inspection documentation with attention to detail in a regulated manufacturing environment

Qualifications

• 5+ years of Quality Control experience in manufacturing with a strong focus on in-line inspections.
• Medical Device industry experience and familiarity with FDA/ISO 13485/GMP requirements.
• Experience performing visual inspections, product reviews, and documentation reviews.

Responsibilities

• Perform in-line inspections of assemblies and finished products.
• Maintain inspection records and documentation in ERP and quality systems.
• Support regulatory compliance and quality assurance activities.
• Work independently on an off-shift schedule and meet quality targets.

Skills

Quality Control

In-line inspections

Medical device knowledge

ERP proficiency

Documentation

Independent work

Attention to detail

Receiving inspection

Regulated manufacturing

Tools

ERP system

Job description

Job Description

Insight Global is seeking a Quality Control Inspector for a medical device client in the Irvine, CA area. This individual will support manufacturing operations by performing in-line inspections of assemblies and finished products to ensure compliance with company quality standards and regulatory requirements.

This is a 3nd shift position scheduled Friday, Saturday, and Sunday 5am-5:30pm. Due to the nature of the schedule, the ideal candidate must be capable of working independently, making sound quality decisions, and effectively managing their workload with limited oversight.

Skills and Requirements

• 5+ years of Quality Control experience in a manufacturing or production environment, with a strong focus on in-line inspections
• Medical Device industry experience
• Experience performing visual inspections, product reviews, and documentation reviews
• Strong ERP system experience
• Strong computer skills and ability to accurately document inspection findings
• Ability to work independently with minimal supervision on an off-shift schedule
• Exceptional attention to detail and commitment to quality standards
• Receiving inspection experience
• Experience working in a regulated manufacturing environment (FDA, ISO 13485, GMP)

We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to [e-mail].