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Sr Engineer

Baxter Healthcare


Location:
Cleveland, Mississippi
Date:
07/31/2017
2017-07-312017-08-30
Job Type:
Employee
Job Status:
Full Time
Categories:
  • Circuits and Systems
  • Control Systems
  • Design/Development Engineering
  • Electronics Engineer
Baxter Healthcare
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Job Details

Description

 

Baxter provides a broad portfolio of essential renal and hospital products, including home, acute and in-center dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; surgery products and anesthetics; and pharmacy automation, software and services. The company’s global footprint and the critical nature of its products and services play a key role in expanding access to healthcare in emerging and developed countries. Baxter’s employees worldwide are building upon the company’s rich heritage of medical breakthroughs to advance the next generation of healthcare innovations that enable patient care.

 

  • Position is key role in the Injection Molding and Plastics Processing Operations.  Primary focus will be on implementing Multi-Variant Data Analysis (MDVA) applications for continuous improvement projects along with associated new business projects that will include MVDA.  Additional focus will be on general project and process support work within the Plastics Processing Operations.  Cross-functional project management will be involved in this role as well.
  • Design/modify precision assembly and/or manufacturing equipment.
  • Manage multiple projects with minimal supervision.
  • Prepares estimates for various tasks and projects.
  • Manage capital projects directly and through coordinating engineers.
  • Drive continuous improvement activities.
  • Interface with plant and corporate groups as well as contractors and vendors.
  • Start-up, debug, and commission new manufacturing processes.
  • Provide technical support/troubleshooting to all plant operations.
  • Demonstrate proactive communication and problem solving.
  • Responsible for supporting and achieving Value Improvement Projects (VIPs).
  • Responsible for adhering to FDA Design Control standards at all times.
  • Responsible for adhering to and maintaining all department Standard Operating Procedures (SOPs), forms and log books.

Requirements

Qualifications

 

  • Bachelor degree in Engineering required (Mechanical, Industrial, Electrical, or Computer degrees are preferred) and 3-5 years related engineering/manufacturing experience (in FDA regulated industry preferred).  Or MS in Engineering with 0-2 years related experience.
  • Programming/troubleshooting experience with automation controls, automated assembly, control systems, PLCs, HMIs, servos and vision inspection systems is preferred.
  • Plastics experience such as plastic bottle blow molding, plastic component injection molding, liquid silicone molding, or film/tubing extrusion is a plus.
  • Project Management skills and experience are a plus.
  • Lean manufacturing skills and experience are a plus 
  • Six Sigma Green Belt or Black Belt certification is a plus

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