Quality Engineer Salary at Safari Circuits BETA

***This is not a Software / IT Quality role*** ***This is a Plant Floor, Automotive Manufacturing Product Quality Engineering role*** ***Sponsorship will NOT be provided now or in the future. This candidate will be responsible for the development, implementation, maintenance, and improvement of quality engineering processes. Throughout the implementation and maintenance process, this candidate should use data analysis to better understand quality reporting measures and improve processes. Candidate Profile 4+ years' of automotive manufacturing experience Strong knowledge of quality tools used in the industry Root Cause Analysis Analytical and quantitative approach to problem solving Bachelor's degree or equivalent in Mechanical, Electrical, or Manufacturing Engineering Responsibilities Perform problem identification, resolution, loss reporting and continuous improvement Design and implement methods for process control, process improvement, testing and inspection Develop, execute, and an

Senior Quality Engineer About the Company Our client is a leading manufacturer known for producing high-performance, energy-efficient products that support essential industries such as health, safety, and infrastructure. With a strong commitment to American manufacturing, they continue to invest in innovation and sustainability, earning industry accolades, including multiple Energy Star Partner of the Year awards. Operating across multiple U.S. locations, they prioritize quality, customer satisfaction, and continuous improvement in all aspects of their business. About the Role Our client is seeking a Senior Quality Engineer to join their team in Middleville, MI. This role will be responsible for improving quality systems, reducing defects, and standardizing processes within manufacturing operations. The ideal candidate will lead PFMEA, Control Plan development, and structured problem-solving initiatives while supporting new product and process development. This is an opportunity to dri

Key Responsibilities: Lead and support EU MDR implementation projects and remediation activities. Review, redline, and approve technical documentation and change orders for MDR compliance. Coordinate and execute the label verification process with local Quality Engineers. Assist in the development and execution of FAI, inspection protocols, and product testing. Ensure project deliverables are completed on time and in compliance with EU MDR standards. Participate in IQ, OQ, and PQ validation activities as required. Collaborate with cross-functional teams including Engineering, Manufacturing, and Regulatory Affairs. Support design and implementation of inspection and testing methods for MDR-compliant product lines. Review and update process and quality documentation, ensuring alignment with MDR standards. Provide statistical analysis and recommend corrective actions for non-compliant materials or processes. Top Skills & Qualifications: Required: 2–4 years of direct EU MDR compliance/reme

Summary The Quality Engineer supports and promotes plant wide quality improvement efforts. Lead and maintain PPAP Process and supporting functions. Evaluate and develop improvement techniques for quality and reliability. Maintain and report on the quality management systems using Process Audits (Layered, Flex-N-Gate, Customer required, Control plan audits). Works with employees, suppliers and customers to produce quality products that meet or exceed the customer and plant's requirements. Coordinates Corrective Action and Continuous Quality Improvement. Core Competencies Customer Focus Communication Team Work Problem Solving Time Management Creative and Innovative Thinking Development and Continual Learning Research and Analysis Decision Making and Judgement Providing Consultation Planning and Organizing Mathematical Reasoning Accountability and Dependability Ethics and Integrity Analytical GDT/Blueprint reading Engineering specifications and understanding Job Duties Handle customer iss

**CANDIDATES CURRNETLY WORKING UNDER F1 OPT/F1 OPT STEM/H1-B WILL NOT BE CONSIDERED. W2 CANDIDATES ONLY** Sr. Quality Engineer (12 month contract // Grand Rapids, MI): Onsite or hybrid (with mandatory 3 days onsite including Monday, Wednesday & Fridays with some rotation to support when necessary) Top 3 Skills: Quality Engineer experience in a medical device setting Experience and capability to work in a fast-paced environment EU MDR compliance experience is strongly preferred Description: This position will support all cardiac surgery EU MDR implementation projects to create/ review and approve change orders, redline the technical documentation, actively lead the label verification process in collaboration with quality engineers at Grand Rapids. Support all other EU MDR related deliverables for the MDR team as appropriate. Education Required: Bachelor’s Degree e.g. Biomedical Engineering, Mechanical Engineering, or similar Years’ Experience Required: 2-4 years of direct EU MDR complia

Sr. Quality Engineer (12 month contract // Grand Rapids, MI): Onsite or hybrid (with mandatory 3 days onsite including Monday, Wednesday & Fridays with some rotation to support when necessary) Top 3 Skills: Quality Engineer experience in a medical device setting Experience and capability to work in a fast-paced environment EU MDR compliance experience is strongly preferred Description: This position will support all cardiac surgery EU MDR implementation projects to create/ review and approve change orders, redline the technical documentation, actively lead the label verification process in collaboration with quality engineers at Grand Rapids. Support all other EU MDR related deliverables for the MDR team as appropriate. Education Required: Bachelor’s Degree e.g. Biomedical Engineering, Mechanical Engineering, or similar Years’ Experience Required: 2-4 years of direct EU MDR compliance/remediation experience Duties: Develops, modifies, applies, and maintains quality standards and protoc

Sr. Quality Engineer (12-month contract // Grand Rapids, MI): W2 ONLY - no C2C or visa sponsorship**************************** Onsite or hybrid (with mandatory 3 days onsite including Monday, Wednesday & Fridays with some rotation to support when necessary) Top 3 Skills: Quality Engineer experience in a medical device setting Experience and capability to work in a fast-paced environment EU MDR compliance experience is strongly preferred Description: This position will support all cardiac surgery EU MDR implementation projects to create/ review and approve change orders, redline the technical documentation, actively lead the label verification process in collaboration with quality engineers at Grand Rapids. Support all other EU MDR related deliverables for the MDR team as appropriate. Education Required: Bachelor’s Degree e.g. Biomedical Engineering, Mechanical Engineering, or similar Years’ Experience Required: 2-4 years of direct EU MDR compliance/remediation experience Duties: Develo

Who We Are and What We Do Since GNS was founded in 1971, the global footprint has expanded rapidly. The company has expanded to several countries around the world. GNS America was established in 2009. Our core business is in conventional stamping, hot stamping, welding, and assembly. Our tool and die capability offer simulation and full design and build activities. If you want to join a leading manufacturing company, now is the time to plan your future career with us. We are in search of a dynamic team member to join a growing successful company. Hot and Conventional Stamping GNS offers a complete range of stamping equipment. Our stamping facilities can cater to any required automotive and industrial stamping requirements. In our automotive operations, we have a full range of stamping capabilities in the 100 ton to 800 ton range, in multiple locations. Our stamping capabilities span a variety of metals. Laser Cutting GNS is a recognized leader in the use of laser technologies, GNS util