Skip to main content
Tallo logoTallo logo

Find Jobs

Find Jobs Near You – Available Work in Your Location

Skip to job details

Back to Results

Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

The QTI Group

Quality Manager - 1st Shift

Career Insights for Quality Assurance Manager

See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.

Scorecard

Based on Wisconsin data

Review key factors to help you decide if this role fits your goals. How is this calculated?

Were these scores useful?

What they do

A Quality Assurance Manager focuses on prevention of mistakes and defects in manufacturing products. Develops procedures to ensure that quality standards are maintained. Manages all steps related to quality assurance as part of the quality management strategy of a company. May involve leadership of a team of quality assurance supervisors, specialists, and other associated staff members.

$102,440 / year median in Wisconsin

-1% projected decline

Explore Career

Job Description

Quality Manager - 1st Shift The QTI Group - 3.7 Middleton, WI Job Details From $35 an hour 4 hours ago Qualifications Defect resolution root cause analysis ISO standards Preventive action implementation Corrective and preventive actions (CAPA) Production validation processes Biomedical regulatory compliance Supplier quality assurance (SQA)
Full Job Description Summary:
Are you passionate about quality, compliance, and helping bring innovative medical devices to market A local manufacturer is seeking a Quality Manager to develop and lead their Quality department and ensure compliance with FDA and ISO standards. This is a Direct Hire position with 1st shift schedule. Pay consideration starts at $35/hr (higher rates based on experience) plus benefits. This is an exciting opportunity for a hands-on quality professional who enjoys building scalable systems, working independently, and making a meaningful impact within a growing medical device organization. Don't miss out on this opportunity at a growing company. Apply today to be considered! Responsibilities Implement, maintain and continuously improve the QMS Create, review and approve quality system documents Establish and maintain supplier qualifications, evaluations and monitoring Develop and execute process validation activities Lead CAPA and Root Cuse investigations Establish and maintain internal audit program and schedule Qualifications Bachelor's degree in Engineering, Life Sciences or related scientific discipline Previous hands-on quality experience in medical device industry Experience with supplier quality, validation, CAPA, complaints and post market processes Knowledge of FDA QMSR and
ISO 13485
Strong documentation and communication skills #indMMIS