GMP Project Engineer – Medical Device (12-month Contract)

PE Global; Limerick; On-site; EUR 50,000 - 70,000; Full time

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.

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.