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Manufacturing Projects Engineer

CREGG

GalwayFull-timeMid LevelOn-site

Job Description

Manufacturing Projects Engineer – Galway (Hybrid)

About the role:

Our world leading Galway-based medical device client are now hiring experienced Manufacturing Engineers to join their Galway team. Hybrid role offering excellent career development. Successful candidates come from a strong project leadership/validation/equipment or medical device background.

Responsibilities:

  • Leading technical improvement under the team’s VIP program.
  • Lead process improvement programs across people, service, quality and cost dimensions.
  • Liaison with quality and engineering both internal to the plant and externally within the corporation.
  • Participation, where appropriate, in the phase review process and the NPE meetings with respect to new products.
  • Ongoing manufacturing support in order to help the team meet its business objectives of quality, output and cost.
  • Maintain a valid capacity model in co-operation with the line Supervisor and conduct adequate advance planning for required capital.
  • Provide leadership on Lean initiatives.
  • Development and implementation of appropriate supporting documentation, which complies with GMP in conjunction with the other team members.
  • Project planning, in detail, in support of major projects, product/process transfer etc.
  • Evaluates in conjunction with EHS new equipment/processes/chemicals for environmental impact/effect to eliminate or lessen such impacts/effects.
  • Responsible for other projects as assigned by the company.
  • Understandsand complieswith all the regulations governing the quality systems.
  • Develop themselves and team members.
  • Manage delivery of capacity/sustaining projects while focusing on quality, output and cost.

Qualifications and Experience:

  • NFQ Level 8 in a Technical Discipline (Science, Biomedical, Mechanical, Manufacturing, etc.)
  • Minimum 2-5 years’ experience working at an Engineering level,ideally in Medical Device industry or other highly regulated environment desirable.
  • Process & Equipment validations IQ/OQ/PQ

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