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Process Engineer I
Ref No.: 22-09771
Location: Tucson, Arizona
Pay Rate : $ 33.00 - 35.00 /Hour
Process Engineer I
Schedule: 8-5 M-F
Contract Length: 1 Year (extension or permanent placement possible)
Location: Tuscon, AZ
Pay: $35/hr
Participates in efforts to define optimized processes and identify technical challenges based on data and Identify suggestions to improve work processes. This engineer is responsible for support of  successful project completion including necessary reports and approvals using thorough technical and theoretical understanding of numerous manufacturing techniques.  Should be a team player, eager to share knowledge and expertise with others.
  • Analyzes data, evaluates results, forms conclusions and provides/implements process or document improvements.
  • Applies advanced engineering knowledge to projects on manufacturability of designs aligned with supplier’s capability.
  • Executes experiments to optimize manufacturing processes / controls.
  • Utilizes DOE where appropriate.
  • Participates in technical team activities.
  • Participates in project planning, process updates and contributes to experimental design.
  • Prepares and delivers presentations of project results to own or other groups.
  • Monitors work to ensure quality, and continuously promote Quality First Time.
  • Must have the ability to manage priorities based on the needs of the manufacturing area with some guidance from the reporting manager and senior management.
  • Knowledge of biomedical/biotechnology manufacturing.
  • Demonstrates potential for technical proficiency, engineering creativity, collaboration with others, and independent thought.
  • Strong understanding of engineering principles and concepts.
  • Strong computing skills utilizing Microsoft Office tools such as Excel, Word, and Powerpoint
  • Strong teamwork skills.
  • Demonstrated troubleshooting and problem solving skills including the use of designed experiments.
  • Ability to meet project deadlines.
  • Ability to multitask and prioritize with some guidance from management.
Automation & Factory Support specifics:
  • Experience with automated manufacturing equipment and automation technologies.
  • Experience with CAD programs such as Pro/Engineer and/or SolidWorks.
  • Experience in a regulated environment. Knowledge of FDA Quality System Regulations (QSR’s) is a plus.
  • Experience with Lean Systems.
Quality Support specifics:
  • Experience in reagent or instrument manufacturing for a Medical Device or Pharmaceutical company.
  • Experience in a regulated environment. Knowledge of FDA Quality System Regulations (QSRs).
BSEE / BSME in a directly related experience OR
MS degree in a directly related discipline + 2 years of related experience required; OR
PhD degree in a directly related discipline and no experience required.