Project Engineer

PE Global

Limerick

On-site

EUR 50,000 - 70,000

Full time

25 hours ago
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Job summary

PE Global are recruiting a Project Engineer for a leading multi-national client in Limerick. This onsite role is based on an initial 12-month contract.

Provide engineering support to develop or improve equipment and processes, manage small to medium projects, define budgets, validate equipment and processes, and interact with cross-functional teams to ensure safety and compliance under GMP/ISO standards.

Qualifications

  • Hold a relevant degree in production, manufacturing or mechanical engineering.
  • 2–4 years of experience in a relevant engineering role.
  • Experience in GMP or medical device manufacturing is preferred.
  • Familiar with ISO safety standards and validation activities.
  • Ability to apply scientific problem-solving approaches to improve productivity.

Responsibilities

  • Perform project management tasks for small to medium scale projects involving new or existing equipment.
  • Assist in determining budgets and evaluate necessary technology.
  • Propose options to management, customers and stakeholders.
  • Support equipment/process validations per internal requirements and procedures.
  • Negotiate with equipment suppliers and manage cross-functional interfaces.
  • Develop equipment/process/product knowledge to be a local expert.
  • Implement improvements to enhance compliance, efficiency, yields or throughputs.
  • Address non-conformances using NCMR and CAPA processes.

Skills

Problem solving
Statistical techniques (ANOVA)
Cross-functional collaboration

Education

Degree in production/manufacturing/mechanical engineering
2-4 years engineering experience
GMP/medical device manufacturing exposure

Job description

PE Global are recruiting a Project Engineer for a leading multi-national client in Limerick. This onsite role is based on an initial 12-month contract.

Job Purpose:

Provide engineering support in developing new or improving existing equipment and/or process related activities. Assist in defining process equipment requirements and specifications based on process requirements, safety requirements and customer needs.

Responsibilities:

Main areas of responsibility:

  • Perform project management tasks for small to medium scale projects involving either new or existing equipment
  • Assist in determining the budget to support requirements
  • Evaluate or assist in evaluating technology necessary to support requirements
  • Propose options to Management/Customer/Stakeholders
  • Support and/or develop and execute equipment or process related validations in accordance with IML requirements, processes and procedures
  • Assist in negotiation with equipment suppliers
  • Utilize necessary project tools, i.e. URS, Microsoft Project, etc. to manage projects successfully
  • Develop the necessary equipment, process and product knowledge to be recognised as a local expert.
  • Measure/evaluate equipment efficiencies, downtime and assist in the development of maintenance requirements
  • Propose and implement improvement projects that improve compliance, improve efficiencies, yields or throughputs
  • Define root cause and implement solutions to equipment and process related non-conformances utilising the NCMR and CAPA processes
  • Actively interfacing with cross-functional team members, always practicing good team work in support of day to day operating requirements
  • Implementation of safety/environment requirements on purchase and changes of all new and existing equipment.
Education and Experience Required for Role
  • Hold a relevant degree or equivalent qualification in production, manufacturing or mechanical engineering.
  • 2 - 4 years’ experience in relevant engineering role
  • Prior experience in a GMP or medical device manufacturing environment
  • Prior experience in equipment and process validation activities
  • Familiar with ISO safety standards
  • Previous experience in the use of ‘black belt’ statistical techniques would be a distinct advantage, as would familiarity with equipment validation in a FDA environment
  • Have statistical process control and capability analysis using ANOVA and
  • Ability to apply a scientific approach to problem solving, blending analytical
  • and experimental skills to maximize productivity and yields is an essential requirement.
Other Skills and Attributes
  • Develop good working relationships across the business
  • Ability to motivate and lead - must be team orientated
  • Ability to work on own initiative
  • Good project management and communication skills.

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***

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