Quality Engineering Technician

Are you ready to work for a company that truly cares about making a meaningful difference in this world?

Culture

Join a team that makes innovations reality, owns the process and demands excellence all while supporting your work-life balance with flexible schedules, ample vacation time to rest and recharge, and a relaxed atmosphere so you can focus on what matters — doing good work that makes people’s lives better. 

We value people that are highly motivated, self-starters open to learning new things every day. We’re looking for people with a good attitude and strong character who strive to be the best at what they do, take accountability for their actions and are determined and committed to get the job done. 

Benefits

We’re a company that values you and your career path and recognizes the importance of work-life balance. 

In addition to being part of a locally owned and operated business who values treating everyone with integrity and respect, we offer the following benefits to our employees:

Employee and/or Employee + Child(ren) medical insurance costs you just $1/month!

Comprehensive Dental + Vision

401k Retirement Plan that we match up to 3%

Basic Life AD&D Insurance

Employee Assistance Program

Paid time off — 18 days first year (pro-rated)

Paid holidays — 9 days

Annual Performance Bonus Potential

Employee Profit Sharing

Tuition Assistance

Shift differential: 2nd shift – + $1/hr, 3rd shift – + $3/hr

We pride ourselves on being a community-minded company that provides lots of opportunity to learn, grow and be at your best every day. 

Position Summary

Reporting to Quality Manager, the Quality Engineering Technician plays a crucial role in ensuring the production of high-quality products while maintaining and improving our quality management systems to meet regulatory requirements.  The ideal candidate must be able to work independently and as a team, have a strong work ethic, a positive attitude, and strong commitment to quality.

How You’ll Make an Impact

Perform root cause investigations of non-conformities; implementing corrective and preventative actions to prevent recurrence.

Support Corrective and Preventive Actions (CAPA) to continuously improve the quality management system.

Maintain the computerized maintenance management system by entering new equipment and equipment changes.

Support the calibration program by ensuring timely completion calibrations.

Create and implement effective quality controls by establishing monitoring, sampling, and inspection methods.

Lead and participate in the development and implementation of quality systems, records, and procedures to ensure compliance with applicable regulatory requirements, standards, and company policies.

Support internal audits to assess the effectiveness of the quality management systems.

Conduct regular inspections and audits to identify defects, deviations, or non-compliance issues.

Provide training and support to employees to ensure adherence to quality standards.

Support external audits from regulatory bodies and customers.

Identify, champion and support continuous improvement projects in quality, productivity, and/or safety.

Support quality metrics trending and analysis.

Perform lot history record review, releasing manufacturing lots and issuing certificates of conformance to customers.

Serve as a subject matter expert in quality assurance on cross-functional teams ensuring compliance to the compliance with applicable regulatory requirements, standards, and company policies.

What You Must Bring to This Role

Minimum two (2) years experience working in a Quality Department in a manufacturing environment.

Experience within Medical Device or other regulated industries preferred.

Strong analytical and problem-solving skills

Familiarity with quality management systems and tools

Detail-oriented with a focus on root cause analysis

Excellent interpersonal skills, with ability to collaborate with and support all levels of associates

Demonstrated ability to assess priority, complete tasks, and work independently

Demonstrated verbal and written communication skills, organized and effective technical writing

Working knowledge of ISO 13485

Working Conditions & Physical Efforts

Work is performed in a Production environment

May be required to lift up to 50 lbs.

Ability to stand or sit for a prolonged period of time

Visual functions being those of acceptable or corrected near vision, depth perception, and ability to adjust focus

Talking and hearing occur continuously in the process of communicating with associates, leadership & suppliers

Finger dexterity is needed to access, enter, and retrieve data using a computer keyboard or operate equipment

Moderate exposure to physical risk

Praxis is an equal opportunity employer