Apqp Jobs in Elkhart

Job Title: Manufacturing Quality Engineer Location: Eden Prairie, MN (Onsite) Must have Skills: DFMEA, PFMEA, APQP, Work Instructions, Rate Routing generation, ECR, ECO's etc (windchill), 3D CAD. Duties / Tasks: Daily fast response shopfloor meetings - participate / contribut More...

Job Title: Sr. Manufacturing Project Engineer Location: Lafayette, Indiana Onsite Fulltime /Contract Job Description & Skill Requirement: 1. Implement creative solutions and validate effectiveness of changes including documentation and training of those improvements. 2. Identif More...

Product development engineer (Metallurgy) Near Savannah, Georgia Full time direct hire Full benefits Relocation No visa sponsorship (US citizen or Green Card only) We have an immediate opening for a Product Development Engineer to manage technical resources, troubleshoot processes to More...

Responsibilities: Provide support to the engineering, manufacturing, logistics, and quality functions within a project scope. Document and communicate the results of problem solutions and conduct analytical examinations to both internal and external customers. Advocate More...

Responsibilities: Coordinate all activities pertaining to ISO 13485 quality management system and FDA 21 CFR 820 quality systems regulation including continuous improvement, and quality assurance. Maintain, monitor, and update QMS forms, procedures, and work instructions. Ensure cu More...

Job SummaryPlans, coordinates and directs the ACTIA quality program. As the quality team leader, you will be expected to direct all quality department associates in regards to the organizations policies and practices. As management quality representative you will be responsible to mai More...

Summary:Work as a hands-on working member of the Engineering team to assist all departments in producing a smooth, efficient flow of quality work through the company. This person will have a more in-depth understanding of the products and processes, and how their work affects and inte More...

Responsibilities: Coordinate all activities pertaining to ISO 13485 quality management system and FDA 21 CFR 820 quality systems regulation including continuous improvement, and quality assurance. Maintain, monitor, and update QMS forms, procedures, and work instructions. Ensure cu More...