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West Pharma Manufacturing Engineer 
United States, Nebraska 
685250374

14.09.2025

Must live within 50 miles of the jobsite or willing to relocate without assistance.

In this on-site role the job holder is a Subject Matter Expert responsible for leading and/or supporting technical engineering projects. Projects will be executed in accordance with internal processes and procedures and in compliance with applicable laws and regulations with internal and external partners. The position holder may have people management responsibilities.

Essential Duties and Responsibilities
  • Managing, planning and executing/supporting technical projects for both production and facility support equipment.
  • Ensuring projects are completed in a safe and timely manner.
  • Assists with equipment repairs by collaborating with the maintenance team through root cause investigations.
  • Acts as a last escalation point for maintenance troubleshooting before they are escalated for outside assistance.
  • Works with vendors in the manufacture and start-up of new equipment, leads qualification completions.
  • Maintains machine, equipment, and facility drawings as needed.
  • Create and update equipment preventative maintenance plans.
  • Create and update procedures related to equipment or processes.
  • Works to ensure plant is in compliance with local, state, and federal environmental regulations.
  • Documentation, monitoring and regular reporting on budget and project status of assigned projects.
  • Interface the technical clarification with internal stakeholders, external planners as well as vendors.
  • Works with HSE and/or Global Safety to ensure equipment meets OSHA requirements, at a minimum.
  • Participate in incident investigations, FMEA’s, and direct completion of corrective actions.
  • Examine See-Do-Say and Continuous Improvement ideas for feasibility, and coordinate completion of approved ideas.
  • Assumes responsibility for material purchasing as required.
  • Utilizes SME network and other company resources to investigate and implement best practices for the facility.
  • Assist MPII program as required.
  • Promotes and supports a Lean environment within the facility.
  • Participate in validation activities as needed, in facility or off-site.
  • Performs other duties as required and/or assigned.
Education
  • Bachelor's Degree in Engineering required
Work Experience
  • Minimum 5 years progressive engineering and leadership experience
  • Experience with facilities, maintenance and equipment repair required
  • Experience in rubber compression molding and or medical device manufacturing preferred
  • Experience in managing projects required
  • Experience with automated systems required
  • Experience with AB and Seimens PLC's preferred
Preferred Knowledge, Skills and Abilities
  • Ability to personnel in all relevant safety requirements related to work standards and equipment requirements
  • Understand and direct personnel in all relevant quality requirements as per the company quality policy
  • Understand all relevant standard operating procedures as per Company policy as they are related to the position covered by this Job Description
  • Support and contribute to Lean programs and activities towards delivery of the plant targets
  • Understanding of facility and production equipment
  • Understand how to read various schematics, including pneumatics, hydraulics, electrical, and mechanical
  • Ability to troubleshoot facility and production equipment issues, and lead maintenance personnel in same activities
  • Ability to present complex issues in a comprehensible manner
  • Process-oriented thinking in combination with a structured, independent and implementation-oriented way of working
Physical Requirements
Medium-Exerting up to 50lb/22kg of force occasionally and/or up to 20lbs/9kg of force frequently, and/or up to 10lbs/4kgs of force constantly to move objects.