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in Jacksonville, FL

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Hours Full-time, Part-time
Location Jacksonville, FL 32202
Jacksonville, Florida

About this job

Job Summary

This position will serve as a technical resource for activities in the manufacturability of custom implants, patient matched implants (PMI), and surgeon specific instruments.

Principal Duties and Responsibilities
  • Conducting feasibility study to estimate product cost and analyze capital equipment capacity and capability 
  • Establishing process methods which meet performance and quality requirements
  • Developing a wide a variety of applications, including machining, finishing, cleaning 
  • Negotiating target completion dates with appropriate personnel from other departments
  • Developing project plans and schedules for work activities
  • Able to work in a fast paced environment
  • Act as a technical liaison between the cross-functional development team and the production facilities, including vendors, for new products
  • Interface with quality and development engineers concerning critical aspects for inspection procedures and gages on new products
Expected Areas of Competence
  • Skilled and knowledgeable in manufacturing and new product processing; Working knowledge of drafting standards and geometric dimensioning and tolerancing
  • Ability to balance manufacturing, and design requirements to meet customer requirements
  • Demonstrates ownership of and ability to manage project assignments with a broad scope and high level of complexity and able to prioritize and complete work in a timely manner
  • Demonstrates problem solving skills through the use of quality and statistical tools
  • Ability to effectively work within a team and cross functionally to expedite completion of critical project tasks 
  • Microsoft Office Suite and Project; Statistical Process Control skills; proficient in process development, and 3-D modeling software
  • Should be able to perform process characterization, qualification and capability analysis
  • Be able to write protocols and reports for process-related testing and validations including process validations, packaging validations, and sterility validations (EO/Gamma)

 

Education/Experience Requirements
  • Minimum B.S. degree from an ABET accredited school (or global equivalent) in one of the following engineering disciplines
  • 3+ years of experience: Mechanical Engineering, Mechanical Engineering Technology, Biomedical Engineering, Bioengineering, Biomedical Engineering Technology, Bioengineering Technology, Aerospace Engineering or Aeronautical Engineering
Travel Requirements
  • Up to 10%
Additional Information

EOE M/W/Vet/Disability.