Search Jobs: Results: Medical Device Quality Engineer (multiple) - Design Control, Specification Development & Continuous Improvement
The Challenges for a Quality Engineer who if offered one of these multiple opportunities include leading continuous improvement initiatives primarily in the New Product Development area of Quality, Manufacturing and Process Engineering.
Salary: Base salary should be from a low of 80's to 90's. The benefits, incentive compensation, stability and relocation package are at the top of the industry.
Location: Multiple roles exist in New Jersey and Arizona.
Contact: Apply below and/or contact Ira Mann at iram@fpccareers.com
So if you are a talented quality engineer who wants further your existing product development and experimental design skills you will also be challenged with:
• Being the Engineering teams Subject Matter Expert on Quality Engineering and Design Controls
• Assuring product specification development, test method development, and risk management are within scope
• Utilizing experimental design, fundamentals of probability, and statistical process control tools to assure reliability, process maintainability, and product safety
• Leading design control assurance and providing an appropriate engineering/technical assessment of data/documents supporting the design history file.
Qualifications:
While a BS and at least 3 years of medical device experience as a process engineer or quality engineer is required, MOST IMPORTANT is to highlight either on your resume, addendum or cover letter your experience with:
1) Test specification development or utilizing experimental design / DOE’s in the medical device industry.
Preferences:
- Verification/validation of manufacturing equipment and processes
- Catheter, delivery systems, Nitinol, ePTFE and/or interventional products experience
- Design control and Design verification, design validation and design history files experience.
- Experimental design, fundamentals of probability and/or statistical process control
- Product specification development, test method development, and risk management
- Mechanical Engineering degree and experience
Key Words: design control, design history file, design verification, design validation, DOE, test specification development, ePTFE, Nitinol, catheter delivery systems, and/or interventional products, experimental design, SPC, process maintainability, product safety
Job Details
| Name: | Ira Mann | Date Posted: | 2/01/2010 |
| Office: | Atlanta | Telephone: | (770) 246-9757 |
| Email: | iram@fpccareers.com | Fax: | |
| Category: | Medical Device, Process Engineer, Product Development, Quality Engineer, Six Sigma/Lean Implementation | ||
| Keywords: | design control, design history file, design verification, design validation, ePTFE, Nitinol, catheter delivery systems, and/or interventional products, experimental design, SPC, process maintainability, product safety | Region: | |
| State: | AZ | City: | |
| Education: | BS | Job Number: | J14104-ATLA-14727-IM |
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