Apqp Jobs in Austin

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...

Industrial Engineer **Position will be located in Austin, TexasResponsibilities:It is the responsibility of the Industrial Engineer to plan, design concepts, evaluate, optimize, write specifications, follow-up with suppliers light industrial equipment including: assembly facilities, w More...

Essential Functions/Duties Fulfill customers Quality deliverables for all project requirements. Support new development process and ensures supplier involvement throughout the project stages and work with supplier to resolve any issue before and after SOP Manage al More...

The QUALITY MANAGERmanages the daily operations of quality and lean activities, including quality system and audits, continuous improvement programs, operational safety, and regulations requirements coordination. Manages staff and associated resources for quality-assurance coverage; b 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...

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...