Manufacturing Projects Engineer- Galway Hybrid

Cregg Recruitment; Galway; Hybrid; EUR 60,000 - 80,000; Full time

Job summary

Cregg Recruitment client in Galway is seeking a Manufacturing (Equipment) Engineer to join their team on a hybrid basis. The role focuses on leading equipment/process validation, lean improvements and delivering cost-quality targets within a highly regulated medical device environment.

Applicants should have NFQ Level 8 in a technical discipline and 2–5 years as an engineer in manufacturing, with experience in IQ/OQ/PQ, CAPA and NPI processes.

Qualifications

• NFQ Level 8 in a technical discipline is required.
• 2–5 years’ experience at an engineering level, ideally in medical device or highly regulated environments.
• Experience with process and equipment validations IQ/OQ/PQ is desirable.

Responsibilities

• Lead technical improvement under VIP program and drive process improvements across quality, service and cost.
• Liaise with quality and engineering internally and externally within the corporation.
• Support phase reviews, NPE meetings and capital planning for capacity.
• Provide leadership on Lean initiatives and develop documentation compliant with GMP.
• Manage projects related to major transfers and ensure environmental considerations are addressed.

Skills

Project leadership

Lean manufacturing

GMP awareness

Process improvement

Education

NFQ Level 8 in Technical Discipline

Tools

IQ

OQ

PQ

CAPA

NPI

Job description

Job Description

Manufacturing (Equipment) Engineer

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 teams 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. Project Planning/Management experience highly desirable. Process & Equipment validations IQ/OQ/PQ

INDTRAC Skills:

• IQ
• OQ
• PQ
• CAPA
• NPI
• TPBN1_IJ