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Engineering Manager
| Reference: | TG - Engineering Manager - Galway | Location: |
Galway Galway City |
| Qualification: | Degree | Experience: | 7-9 Years |
| Job Type: | Permanent | Salary: | Not Disclosed |
Title: Engineering Manager
Location: Ballybrit,Galway
Benefits: Competitive salary, bonus, pension and healthcare
Company:
My client is a Specialized center of excellence for designing, developing, and manufacturing high-performance medical balloons and balloon catheters. Supporting R&D, prototyping, small batch, and full-scale commercial production, the site delivers end-to-end solutions for minimally invasive medical devices
Role:
he Engineering Manager will lead and oversee all engineering activities within a dynamic medical device contract manufacturing environment. This role focuses on maintaining and improving existing manufacturing processes, driving operational excellence, and ensuring compliance with regulatory standards (ISO 13485, FDA). The Engineering Manager will champion continuous improvement initiatives, cost reduction strategies, and safety enhancements to support long-term business growth and customer satisfaction.
Responsibilities:
Leadership & Team Developmenr
- Manage and mentor a team of engineers and technicians, fostering a culture of accountability, collaboration, and innovation.
- Develop team capabilities through training, coaching, and performance management.
Sustaining Engineering
- Provide technical support for existing products and processes, ensuring stability, efficiency, and compliance.
- Troubleshoot and resolve manufacturing issues to minimize downtime and maintain product quality. Continuous Improvement Implement best practices in process optimization and automation.
Cost Reduction
- Identify and execute cost-saving opportunities in materials, processes, and equipment without compromising quality or compliance.
- Collaborate with supply chain and operations to optimize resource utilization. Safety & Compliance
- Promote a strong safety culture and ensure adherence to health and safety regulations.
- Maintain compliance with ISO 13485, FDA, and customer-specific requirements in all engineering activities. Cross-Functional Collaboration
- Partner with operations, quality, and supply chain teams to support production goals and resolve technical challenges.
- Act as a technical liaison for customer inquiries and audits.
Project Management
- Plan and execute engineering projects related to process improvements, equipment upgrades, and capacity expansion.
- Ensure projects are delivered on time, within scope, and budget.
Requirements:
- Bachelor’s degree in Mechanical, Manufacturing, or Industrial Engineering (Master’s preferred).
- Minimum 7+ years of engineering experience in a regulated manufacturing environment, preferably medical devices.
- 3+ years in a leadership or managerial role.
- Strong knowledge of ISO 13485, FDA regulations, and GMP requirements
Does this sound like your next career move for 2026? To apply and For more info forward your application to the link provided or contact me on 087 0612325 OR thomas.gallagher@lifescience.ie
Biotechnology | Tel:+353 1 685 4545 | Fax: +353 (0)1 443 05 24 | Email: info@biotechnology.ie
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