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1)Title: Mechanical Engineer
Location: Goleta, CA

Position for Mechanical Engineer - Goleta, CA. This is a 4+ Months contract position. The Hourly rate is DOE. Client is looking for Local candidates only.

Job Description:

• Evaluating "Specials" products versus current products from an engineering viewpoint.
• Evaluating if the Specials design, materials and manufacturing (e.g., assembly method and inspection / test methods) are the same as the current products, and determining if additional testing is required.
• Writing technical documents (e.g., documenting the results in an assessment).
• Will be working on mostly long term implants (e.g., catheters, valves, reservoirs), generally made of plastic, silicone and RTV silicone adhesive.
• Needs to have good drawing, print and specification skills and experience.
• Needs design and manufacturing engineering expertise with silicone and plastic components.
• Must have experience with design controls, process validations, and design verification.
• Needs experience with doing line extensions to 510(k) released products.

This is not a drafting or design role. No cad programs will be used for this role. No telecommuting. Required Experience:

• Medical device experience is a MUST!
• 3+ yrs experience.
• Design and manufacturing engineering expertise with silicone and plastic components is a must.
• Experience with design controls, process validations, and design verification needed.
• Education Level: Undergraduate Degree or equivalent experience
• Industry Experience: 1 - 3 Years

• Education Level: Graduate Degree
• Industry Experience: 3 - 5 Years

2) Title: Manufacturing Process Engineer
Location: Memphis, TN

Opening for Manufacturing Process Engineer - Memphis, TN. This is a 10+ Months contract position. The Hourly rate is DOE. Client is looking for local candidates only.

-Responsible for the development, qualification, documentation, and control of manufacturing and assembly methods and processes in support of new product launches.
-Responsible for the coordination and execution of validation projects.

-Responsible for the development, qualification, validation, documentation, and control of manufacturing and assembly methods and processes in support of product launches.
-Work with, but not limited to, Research and Development, Marketing, Quality, Regulatory Affairs, Material Planning, Strategic Procurement, Distribution, Manufacturing facilities and suppliers to provide or secure information, coordinate activities and solve problems.
-Assist in the prevention and resolution of technical production issues and validation issues with assigned products by working with manufacturing and quality personnel at Medtronic facilities and suppliers.
-Travel as required for company business transactions. Amount of travel could be extensive at times. Could include, but not limited to, visits to Medtronic manufacturing and Distribution facilities, implant/instrument suppliers, equipment suppliers. Experience:
-Candidate needs medical industry process validation experience. Also needs Manufacturing Engineering experience.
-Must have 4 year Engineering Degree; prefer Mechanical or Manufacturing Engineering Degree.
-Industry Experience: 3 - 5 Years
-Project Management: Concurrent Project Management, Project Coordination, Project Recordkeeping and Documents
-Six Sigma/Lean Sigma Certifications: Green Belt Black Belt
-Travel: 25-50% Travel
-Written Communication: Excellent