Manufacturing Engineer II – EO Sterilization Specialist

Boston Scientific; Connacht; On-site; EUR 50,000 - 65,000; Full time

Job summary

Boston Scientific in Galway seeks a Manufacturing Engineer P2 on a permanent basis to support Ethylene Oxide Sterilization and drive process improvements. The role focuses on daily operations, troubleshooting, and project work to optimise production cycles.

The ideal candidate brings a strong engineering background, 5+ years in related fields, and the ability to lead cross-functional initiatives while ensuring safety and quality in a medical device environment.

Qualifications

• NFQ Level 8 Major Award in Materials/Engineering with a minimum of 5 years' work experience.
• Experience with Ethylene Oxide sterilization systems and cycle validations is advantageous.
• Excellent technical capabilities, communication, teamwork and initiative.
• Able to work well in a team and independently with minimal supervision.
• Experience in medical device, electrical, sterilization or mechanical fields preferred.

Responsibilities

• Provide daily operational support to Ethylene Oxide Sterilization area while completing improvement projects.
• Develop, troubleshoot, standardise, and improve sterilization methods and cycles.
• Champion safety practices and implement improvements in the area.
• Liaise with Sterilization Operation sites, QA, Facilities, Health and Safety, and Materials handling.
• Lead equipment improvement projects and provide training to technicians.

Skills

Technical capabilities

Communication skills

Teamwork abilities

Initiative

Problem solving

Education

NFQ Level 8 Major Award in Materials/Engineering

Job description

Boston Scientific in Galway seeks a Manufacturing Engineer P2 on a permanent basis to support Ethylene Oxide Sterilization and drive process improvements. The role focuses on daily operations, troubleshooting, and project work to optimise production cycles.

The ideal candidate brings a strong engineering background, 5+ years in related fields, and the ability to lead cross-functional initiatives while ensuring safety and quality in a medical device environment.