Senior Mechanical Design Engineer
| Company | Kreg Therapeutics, Inc. |
| Location | Chicago, IL |
| Discipline | Mechanical Engineering |
| Posted | 11-04-2009 |
Job Description
Kreg Medical, Inc., a medical device manufacturer based in Chicago, is recruiting for an experienced Senior Mechanical Design Engineer to aid in the development and manufacturing of specialty medical products.
Responsibilities:
Plans, organizes, directs and conducts engineering processes to develop new product designs and specifications from concept and prototype through manufacturing and launch. Typical responsibilities include, but are not limited to the following:
Planning realistic rapid development time schedules.
Performing complicated engineering assignments involving specification, design, manufacturing, prototyping, launch and revisions.
Develop CAD models using Solidworks
Optimize new product designs & specifications through development of engineering drawings to meet regulatory and schedule requirements.
Provide regular feedback that creates ideas and solutions to decrease time to market and improves new product development process.
Responsible for entire product life cycle.
Collaborate with outside fabricators to quote and produce new product prototypes
Work with vendors to source new materials
Management and development of standards for CAD data system
Development of knowledge of applicable regulatory requirements and proper documentation of all activities to satisfy FDA quality system requirements
Other responsibilities as business objectives evolve
Qualifications:
The following areas of experience are requirements for this position:
7-10 years of design engineering experience is REQUIRED
Bachelors Degree in Mechanical Engineering from accredited University is required. Masters Degree in Engineering is preferred.
Strong project management experience.
Self-starter with ability to ask questions and deliver assignments under tight timelines with little supervision.
Strong background in material selection and application.
Background in medical equipment industry is a plus.
Hands on mechanical skills and experience in machine shop / prototyping environment
Comfortable sourcing vendors for fabrication from prototype to production
3+ Years industry experience with Solidworks 3D CAD platform REQUIRED
Proficient in complex electromechanical assembly design
Experience designing parts for the following manufacturing processes:
Sheet metal
General machining
Welded frames
Injection molding
Knowledge of loading and safety factor calculations
Experience designing experiments to test prototype functionality
Experience designing for manufacturability, assembly, and serviceability
An ideal candidate would also have experiences or skills in the following areas:
Familiar with Document Controls & Document Change Processes
Familiar with Product Design Verification & Validation Processes
Expertise with Microsoft Word, Excel and PowerPoint
Familiarity with meeting regulatory requirements such as UL, IEC, etc.
Familiarity with FDA quality systems is a plus.
Responsibilities:
Plans, organizes, directs and conducts engineering processes to develop new product designs and specifications from concept and prototype through manufacturing and launch. Typical responsibilities include, but are not limited to the following:
Planning realistic rapid development time schedules.
Performing complicated engineering assignments involving specification, design, manufacturing, prototyping, launch and revisions.
Develop CAD models using Solidworks
Optimize new product designs & specifications through development of engineering drawings to meet regulatory and schedule requirements.
Provide regular feedback that creates ideas and solutions to decrease time to market and improves new product development process.
Responsible for entire product life cycle.
Collaborate with outside fabricators to quote and produce new product prototypes
Work with vendors to source new materials
Management and development of standards for CAD data system
Development of knowledge of applicable regulatory requirements and proper documentation of all activities to satisfy FDA quality system requirements
Other responsibilities as business objectives evolve
Qualifications:
The following areas of experience are requirements for this position:
7-10 years of design engineering experience is REQUIRED
Bachelors Degree in Mechanical Engineering from accredited University is required. Masters Degree in Engineering is preferred.
Strong project management experience.
Self-starter with ability to ask questions and deliver assignments under tight timelines with little supervision.
Strong background in material selection and application.
Background in medical equipment industry is a plus.
Hands on mechanical skills and experience in machine shop / prototyping environment
Comfortable sourcing vendors for fabrication from prototype to production
3+ Years industry experience with Solidworks 3D CAD platform REQUIRED
Proficient in complex electromechanical assembly design
Experience designing parts for the following manufacturing processes:
Sheet metal
General machining
Welded frames
Injection molding
Knowledge of loading and safety factor calculations
Experience designing experiments to test prototype functionality
Experience designing for manufacturability, assembly, and serviceability
An ideal candidate would also have experiences or skills in the following areas:
Familiar with Document Controls & Document Change Processes
Familiar with Product Design Verification & Validation Processes
Expertise with Microsoft Word, Excel and PowerPoint
Familiarity with meeting regulatory requirements such as UL, IEC, etc.
Familiarity with FDA quality systems is a plus.
How to Apply
Please submit a cover letter along with resume to kregjobs@kreg.us, please put job title in subject line to be considered for position.
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