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Process Development Engineer

Cynet Systems
Maple, MN Contractor
POSTED ON 12/11/2024 CLOSED ON 2/10/2025

What are the responsibilities and job description for the Process Development Engineer position at Cynet Systems?

We are looking for Process Development Engineer for our client in Maple Grove, MN

Job Title: Process Development Engineer

Job Location: Maple Grove, MN

Job Type: Contract

Job Description:

Responsibilities:

  • Collaborates cross functionally to develop robust designs and processes.
  • Assesses process capabilities, prioritizes process improvement opportunities, and innovates and implements process improvements on projects.
  • Applies technical knowledge to innovate, design, and develop processes, procedures, tooling, and/or automated equipment.
  • Writes clean and concise manufacturing work instructions that can be understood by product builders.
  • Writes technical reports, validations, and qualifications by capturing experimental results.
  • Writes validation protocols and reports applicable to new processes.
  • Executes experiments, analyzes results using standard statistical methods, reports out recommendations, and generates next steps to improve performance, process efficiency, and technical understanding.
  • Gathers and provides technical data for technical reviews.
  • Assists in completing proper documentation to meet quality systems requirements. (e.g., BOM’s, Routers, Process Risk Analysis, etc.).
  • Oversees development builds associated with the project using special work requests.
  • Assists in developing qualified production lines.
  • Provides Design for Manufacturability (DFM) input to the engineering print package.
  • Contributes ideas to or generates Intellectual Property submissions.
  • May train manufacturing personnel when required as part of a validation.
  • Build Quality into all aspects of their work by maintaining compliance to all quality requirements.

Minimum Qualifications:

  • 2-5 years' experience with BS in Engineering field.
  • Industry related experience (internships, co-ops can be included in 2-5 years of experience).
  • Statistical background.
  • Candidate will need to have the ability to work cross-functionally and with other sites in order to be successful.

Preferred Qualifications:

  • Highly motivated individual that can independently drive deliverables to completion through collaboration among team members and internal support staff.
  • Basic understanding of DFM, medical device design control, quality systems, and the product development process (PLCP) is highly desired.
  • Strong statistics background.

Salary : $46 - $46

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