Quality Engineer

GN Group•Shakopee, MN

13d•$80,000 - $95,000•Hybrid

About The Position

GN brings people closer through our leading intelligent hearing, audio, video, and gaming solutions. Inspired by people and driven by innovation, we deliver technology that enhance the senses of hearing and sight. We help people with hearing loss overcome real-life challenges, improve communication and collaboration for businesses, and provide great experiences for audio and gaming enthusiasts. GN was founded more than 150 years ago with a vision to connect the world. Today, inspired by our strong heritage, GN touches more lives than ever with the broadest portfolio of products and services in our history – fostering a sense of community, openness, and understanding. By listening to customers and combining our unique expertise in the human ear, audio, video, and speech, wireless technologies, software, and miniaturization, we transform what it takes to bring people closer to what is important to them. The GN-owned brands that are responsible for bringing these technologies to life: Medical grade hearing technology: ReSound, Beltone, Interton, Jabra Professional collaboration: Jabra, BlueParrott, FalCom Gaming, calls and media: SteelSeries, Jabra Founded in 1869, the GN Group employs 7,000 people and is listed on Nasdaq Copenhagen (GN.CO). GN’s solutions are sold in around 100 countries across the world. If you would like to learn more about us, visit our homepage gn.com or click on our different brands. You can also connect with us on LinkedIn, Facebook and Twitter.

Requirements

Strong verbal and written communication skills
Problem solving skills
Detail oriented
Root cause analysis
Risk assessments
Excellent organizations skills to manage multiple priorities
Self-directed
Drive continuous improvement throughout the organization
Bachelor’s Degree in Engineering or equivalent experience.
2+ years related work experience: (Quality Engineering, Quality Control, Quality Improvement Projects, Root Cause Analysis, CAPA)

Nice To Haves

Experience in Medical Device Manufacturing, ISO 13485, highly preferred.

Responsibilities

Develop and maintain quality system related procedures.
Develop and execute training, including competence assessment, for quality-related processes and procedures
Create, review and approve Engineering and Manufacturing Change Orders
Work cross-functionally to conduct root cause investigation, action planning and verification of effectiveness for CAPA
Work with manufacturing, supply chain, engineering, and others to solve internal and external supplier quality issues; investigate non-conforming product and recommend disposition
Design, supervise, and perform quality methods such as failure mode effects analysis and statistical process control
Establish and maintain systems/methods to monitor incoming, in-process and shipped product quality to ensure safety and performance, identify trends and drive improvements
Communicate with local, global and corporate functions and customers, as needed, to resolve system and product quality issues, including customer complaints
Drive Quality Planning Process including FMEA (Risk Management), Control Plan and Process Audit, etc.
Establish and maintain inspection procedures based on the material/product specifications and customer requirements