We are supporting our Galway based medical device client who are hiring a Manufacturing Engineer to join their core Engineering team. In this role, you will play a vital part in ensuring the efficient and high-quality manufacture of medical devices. Using your technical expertise, problem-solving skills, and validation experience, you will help optimize manufacturing processes, support new product introductions, and drive continuous improvement.
Experience with Balloon Forming is a requirement for this position.
Key Responsibilities:
- Lead and execute tasks within projects, ensuring successful outcomes.
- Implement process controls to ensure robust and repeatable manufacturing.
- Drive continuous improvement initiatives to maximize process performance.
- Apply scientific and analytical approaches to problem-solving and process optimization.
- Ensure all engineering work complies with regulatory, quality, and safety standards.
- Collaborate with Automation Engineering to develop stable, capable new processes.
- Provide technical support for new products, technologies, and process changes.
- Evaluate and correct non-conforming products or processes.
- Complete validations and process improvements using statistical tools and Six Sigma techniques.
- Support the development of in-house subject matter expertise across core technologies.
- Participate in process, equipment, and health & safety risk assessments.
- Provide progress updates to senior management and support routine manufacturing meetings.
- Maintain and report key manufacturing metrics on a weekly basis.
Qualifications:
- Bachelor’s or Master’s degree in Engineering (or equivalent).
- 3–5 years’ experience in a Manufacturing Engineering role within the medical device or healthcare industry.
Skills & Experience:
- Experience with balloon forming is required.
- Proven success in implementing continuous improvement initiatives.
- Proficiency in CAD software.
- Strong report writing, documentation skills, and attention to detail.
- Knowledge of regulatory requirements, quality standards, and GMP practices.
- Experience with validation and qualification (IQ, OQ, PQ) of equipment and processes.
For more information and a confidential discussion on the role please contact Amy Newell.
amy.newell@collinsmcnicholas.ie
091 706718
