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Posted by: CCSI Inc - Robert Ryder <robert@ccsiinc.com> on September 23, 2009 at 12:15:49. Click here to reply to this post via Email.

Contract / Temp to Perm / Permanent: Contract
City: Northridge
State: California
Country: United States

Design of Experiments (DOE) and Statistical Process Control (SPC),Determines manufacturing operation requirements and process parameters ,Develops plans to evaluate process repeatability and stability ,Develops product and process improvements, Participates in internal supplier audits, Participates in procedure writing and review ,Performs process and equipment validations ,Provides technical support to other engineers ,Reviews product performance data to identify trends, Supports manufacturing, development, and implementation processes, Ensures compliance with GMP’s,Generates documentation for engineering protocols and reports ,Implements quality system improvements ,Writes engineering and manufacturing specifications

Responsibilities: As a Sr. Mechanical Engineer, you will provide technical solutions to a wide range of difficult problems. Your solutions should be imaginative, thorough, practicable and consistent with organizational objectives. You will work under only general direction. You will independently determine and develop approaches to solutions. Your work will be reviewed upon completion for adequacy in meeting stated objectives. You will represent the organization as the prime technical contact on contracts and projects. You will interact with senior external personnel on significant technical matters often requiring coordination between organizations. You will be responsible for key aspects of product engineering support when it comes to Mechanical Component Designs and Manufacturing Process Development. You must be able to utilize your personal competencies and leadership skills as part of a fast paced product development and implementation team to quickly and effectively evaluate designs, tooling and manufacturing processes to drive projects to a timely completion. You will also be called upon to evaluate manufacturing facilities and give your recommendations as to their areas of expertise. You will be required to highlight and identify design flaws and offer solutions and have the ability to implement recommended improvements. You will be responsible for writing and implementing process validations and engineering reports. You will be required to function as a liaison between Product Engineering, Manufacturing, R&D and Suppliers. You will participate in continuous improvement projects. You will also be required to use Design of Experiments, Lean/Sigma Tools and/or Statistical Analysis Software to complete assigned projects. Qualifications: •Bachelor's degree in Engineering. •5 + years of hands on engineering experience in a medical device assembly manufacturing environment or equivalent experience. •Must have a complete understanding and wide application of technical principle, theories, and concepts in the field. General knowledge of other related disciplines. •Experience in design for Six Sigma. •Must have completed lean manufacturing projects that followed the DMAIC process •Must have Green Belt Certification with a strong background in statistics •Able to utilize 2D and 3D Solid Works or AutoCAD systems to perform detailed design analysis, including structural, thermal and finite element analysis methods. •An understanding of geometric tolerancing when it comes to component and subassembly designs •Have the ability to implement changes to