Length of Engagement: Direct Hire Employee No Visa sponsorship
Position Description:
The Development Engineer I works in a cross-functional Design Team to develop innovative and creative reprocessing techniques for new products. The Design Teams will integrate user needs into product and process specifications
Responsibilities:
Design experiments and execute testing as necessary. Prepares testing submissions Identifies hazards and performs risk analysis Assist in Standard Operating Procedure creation Creates engineering requirements Creates product requirements Creates process and new material specifications Creates master validation plans Writes and/or assists in the writing of test protocols Creates Instructions for Use Creates design verification and performance qualification testing plans Helps prepare design transfer activities Conducts employee training for new products.
Required Experience:
2-5 years in an engineering discipline Medical device experience preferred Experience in SPC and root cause analysis Technical writing experience in SOP Product development experience preferred Experience working with multiple discipline projects Knowledge of Food & Drug Administration Quality System Requirements (QSR) Part 820 a plus Strong organizational and time management skills Strong mathematical skills Must be able to trouble-shoot and solve problems collaboratively Research skills required Able to work effectively and positively in a team environment Experience in MS Office (Word, Excel, Outlook, PowerPoint, MS Project) 4 year/Bachelor’s Degree in engineering (Mechanical, Biomedical, Electrical, Chemical)
Preferred Experience:
Licensed Engineer preferred
Email your resume with " 410-1203 Development Engineer I " in the subject line to jobs@protechnicals.com
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