Quality Control Technician - 258357

Medix™; Irvine (CA); On-site; USD 52,000 - 64,000; Full time

Job summary

Medix is seeking a Quality Control Technician for the 2nd shift in Irvine, CA to inspect materials and products throughout the manufacturing process, ensuring quality and documentation requirements are met.

The role requires performing visual, dimensional, and functional inspections, reviewing records for accuracy, and entering data in Oracle. GMP/GLP awareness and attention to detail are essential components of this position.

Qualifications

• At least 1 year of experience in a regulated manufacturing environment.
• High school diploma or equivalent.
• Basic knowledge of inspection tools; experience with micrometers and calipers is a plus.
• GMP or GLP experience is a plus.
• Strong attention to detail and a good work ethic.
• Basic computer and data entry skills.

Responsibilities

• Perform visual, dimensional, and functional inspections of raw materials, components, in-process materials, and finished products
• Review donor records and documentation for accuracy and compliance
• Complete quality inspections and documentation during receiving, in-process, and testing activities
• Perform label inspections to ensure accuracy and proper placement
• Audit manufacturing processes to make sure procedures are being followed and materials are properly segregated
• Create and follow up on non-conformance reports (NCRs) through final disposition
• Enter and transact parts and in-process audit information in Oracle
• Assist with special quality projects and other duties as needed

Skills

Attention to detail

Data entry

Computer basics

Education

High school diploma or equivalent

Tools

Micrometers

Calipers

Oracle

Job description

We are looking for a Quality Control Technician to join our 2nd shift team. This role will be responsible for inspecting materials and products throughout the manufacturing process to make sure everything meets quality and documentation requirements.

Responsibilities

• Perform visual, dimensional, and functional inspections of raw materials, components, in-process materials, and finished products
• Review donor records and documentation for accuracy and compliance
• Complete quality inspections and documentation during receiving, in-process, and testing activities
• Perform label inspections to ensure accuracy and proper placement
• Audit manufacturing processes to make sure procedures are being followed and materials are properly segregated
• Create and follow up on non-conformance reports (NCRs) through final disposition
• Enter and transact parts and in-process audit information in Oracle
• Assist with special quality projects and other duties as needed

Requirements

• At least 1 year of experience working in a regulated manufacturing environment
• High school diploma or equivalent
• Basic knowledge of inspection tools; experience with micrometers and calipers is a plus
• GMP or GLP experience is a plus
• Strong attention to detail and a good work ethic
• Basic computer and data entry skills

Preferred Qualifications

• Medical device manufacturing experience
• Cleanroom manufacturing experience
• Quality certifications such as CQIT or similar