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Automation Engineer

Job in Tempe, Maricopa County, Arizona, 85285, USA
Listing for: West Pharmaceutical Services, Inc
Full Time, Contract position
Listed on 2026-09-24
Job specializations:
  • Engineering
    Quality Engineering, Manufacturing Engineer, Automation & Mechatronics Engineer
Salary/Wage Range or Industry Benchmark: 70000 - 100000 USD Yearly USD 70000.00 100000.00 YEAR
Job Description & How to Apply Below

Tempe, AZ, US, 85283

At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life savings and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun.

A name started our story. How will you help write our future?

There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.

We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.

This position is a fixed-term contract projected to last 9 months. The position offers benefits, training, and full-time hours. A $1,000 bonus will be offered for 12 & 24 weeks for those that complete these milestone dates.

Job Summary

In this role, you will be responsible for developing new technology and supporting existing technology to improve production, quality, profitability and safety. This individual will be responsible for the planning, scheduling, execution of projects and communicating project status to targeted timelines. This individual will also manage/assist in facility expansion/modifications.

Essential Duties and Responsibilities
  • Support development of new technology, existing technology and existing production lines to improve quality, profitability and safety.
  • Develop, execute and document project assignments in compliance with committed timelines and project goals, and per established governance policies and procedures.
  • Ensure technical and customer requirements for assigned projects are achieved.
  • Develop and maintain required validation and project management documents.
  • Conduct or participate in routine project reviews with Project Teams and Management
  • Perform design work, layouts, sketches, concepts, etc. as needed for projects and/or plant layouts.
  • Develop and/or review engineering change requests for modifications to processes, equipment and facilities.
  • Troubleshoot and repair of all automation.
  • Evaluate and maintain proper machine safeties to ensure employees are protected when operating any piece of automation.
  • Ensure automation lines are meeting their targeted output and OEE by analyzing production data.
  • Maintain quality finished product through proper maintenance and operation of all automation.
  • 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.
  • Automation includes – assembly machines/fixtures, label applicators, robots, end of arms, separators and test equipment. Any other equipment assigned by management.
Education
  • Education or Equivalent

    Experience:

    4-year technical degree.
Work Experience
  • Minimum 3 years Experience in related industry required
Preferred Knowledge,

Skills and Abilities

  • Background in medical devices/pharmaceutical would be a plus.
  • Knowledge of quality systems requirements, FDA Quality System Regulation, cGMP and relevant ISO standards
Travel Requirements

5%:
Up to 13 business days per year

Physical Requirements

Light-E…

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