Engineer Quality Assurance 2
Location: Brooklyn Park, Minnesota
Description: Accellent is currently interviewing Engineer Quality Assurance 2 right now, this job will be ordered in Minnesota. Detailed specification about this job opportunity please give attention to these descriptions. Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellent www.accellent.com , a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. With approximately 20 locations, Accellent employs more than 3,000 people in 6 countries.
Currently, we are searching for a Quality Engineer to join our Quality Assurance Team at the Brooklyn Park, MN facility.
Position Scope / Summary
Quality Engineer assists in the design and implementation of policies and procedures for testing and evaluating the precision and accuracy of products and/or equipment. The Quality Engineer will be expected to provide support to Operations, interact with customers and provide support for Engineering, Quality Systems and Process engineering.
Required Skills
Specializations may include but are not limited to: design control; material and process control; product reliability; software quality engineering; and/or metrology.
This position will be integral in meeting the Quality Management System requirements. It requires creativity and foresight to work with operations and product development teams to ensure compliance to the Quality Manual, Design Control, Supplier Management and other appropriate procedures for a variety of medical devices from concept through market introduction. The ideal candidate is a self-motivated individual who is excited by the prospect of working in a dynamic, fast-paced environment.
Required Experience
Qualifications:
2-7 years experience in the Medical Device or other regulated industry, such as QSR and ISO 13485, with increasing responsibility.
Experience with FDA and ISO 13485 Certification inspections is a plus.
Must be adept in use of computer software for the analysis of data, preferably Microsoft Excel and statistical packages (Minitab preferred).
Quality Engineering certification (CQE) preferred or equivalent body of knowledge in areas which include but are not limited to Statistics, SPC, Geometric Dimensioning & Tolerancing; Sampling, Design of Experiments, etc. Ability to analyze, understand and effectively communicate this technical material. Experience with Lean Manufacturing and Six Sigma is a plus.
Ability to organize and judge priorities in a dynamic, fast-paced environment and work independently with minimal supervision.
Must possess excellent verbal & written communication skills, which include but are not limited to presentation, organizational and management skills.
Experience working with the following a plus; micro machined components, CNC machining, Swiss & vertical milling style equipment, injection molding and laser welding
- .
If you were eligible to this job, please send us your resume, with salary requirements and a resume to Accellent.
Interested on this job, just click on the Apply button, you will be redirected to the official website
This job starts available on: Sun, 12 Aug 2012 09:11:37 GMT
Apply Engineer Quality Assurance 2 Here