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Sr Controls Engineer

West Pharmaceutical Services
Tempe, Arizona, US
Full-time

Job Summary

In this role, you will be responsible for PLC / controls, programming and troubleshooting of robotics and automation equipment.

Knowledge of industrial vision systems. Develop, build and program automated equipment. Develop continuous improvement plans for all assembly equipment.

Essential Duties and Responsibilities :

  • Evaluate and maintain proper machine safeties to ensure employees are protected.
  • Create drawings and wiring diagrams in SolidWorks.
  • Proficient in vision systems i.e. Cognex, Keyence, etc.
  • Develop, build and program automated equipment to support production.
  • Work closely with the other engineers on PLC programing changes needed to improve processes.
  • PLC / Controls, mechanical troubleshooting and repair of all automation.
  • Coordinate and Perform end of arm repairs and fabrication.
  • Evaluates and maintains accurate documentation of automation repairs and adjustments.
  • Establish and maintain an escalation plan to minimize downtime.
  • Improve line efficiencies using line history and production data.
  • Provide timely notification to shift leaders and program managers of maintenance and down time issues.
  • Interfaces daily with engineering manager and shift support staff.
  • Conforms with and abides by all regulations, policies, work procedures, instruction, and all safety rules.
  • Performs other duties as assigned by management.
  • Exhibits regular, reliable, punctual and predictable attendance .
  • Other duties as assigned.

Basic Qualifications :

Education or Equivalent Experience : Technical degree. 5-10 years’ experience in PLC programming, servicing and

repairing automation and robotics.

Preferred Knowledge, Skills and Abilities :

  • PLC / Controls Engineering.
  • 5-10 years of experience in related industry.
  • Experience in automation equipment used in medical device industry or other regulated industry.
  • Knowledge of quality systems requirements, FDA Quality System Regulation, cGMP and ISO 9002.

Travel Requirements :

Minimal.

Physical and Mental Requirements :

Must be able to work a 40-hour work week, plus overtime and / or irregular hours as required to complete assignments. May stand or sit for extended periods of time.

Must transport oneself to and from other areas of the facility and travel to other divisions when necessary. Must have good visual acuity and distinguish color differences for product and safety issues.

Medical Device manufacturing requires strict adherence to standards. Working environment is a clean room manufacturing facility, which houses plastic injection molding machines.

Must work constructively in an environment that may be stressful due to competing resources while at all times maintaining company confidentiality.

LI-CS1

30+ days ago
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