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Contact Info
Kevin Silke
Life Science

01 507 9255
[email protected]
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Risk Manager
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Republic of Ireland
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Process Development Engineer

Reference:KG-AAMD-126587 Location: Galway
Qualification:DegreeExperience:3-4 Years
Job Type:PermanentSalary: Not Disclosed

Would you like to join a leading medical device company in Galway to further develop your career? This is an excellent opportunity for an experienced Process Development Engineering professional.

You will focus on designing and developing cutting edge technologies for the manufacture of class III medical devices. You will be directly involved in the development of innovative products and processes for use in medical procedures.

• As an engineer you will actively participate in all areas of product transfers including the following: Design, Technology development & advancement, Automation, Vendor management, Manufactuirng & Project management.
• You will support all activities related to equipment development and validation to meet internal and regulatory (CE) requirements.
• You will support process development, characterization and validation activities.
• You will use Design, Reliability & Manufacturability methodology (DRM), 3-D drawing/printing and Augmented reality to develop best in class technologies for the manufacture of our medical device product ranges.
• You will collaborate with cross functional teams to define, execute and deliver on program deliverables.
• You will utilize your new and existing skillsets in six sigma tools, project management and technology development to solve technical problems.
• You will compile, document and present all learnings to project and functional teams.

• Third Level 8 Degree or higher in Electronic, Electrical, Mechanical or Biomedical Engineering or related discipline and desirably with experience in a similar role.
• Dynamic team player and can work effectively and proactively on cross-functional teams
• Knowledge of medical device processes with a good understanding of product and process design.
• Develops technical / Equipment documentation including Equipment binders , Equipment validations and technical reports in accordance with quality system requirements.
• Support the development and sourcing of vendors, Co-ordinate and liaise with vendors to ensure equipment is sourced to budget and on time.
• Supports verification, validation, and implementation of equipment for both design and process development.
• Utilizes knowledge of FDA and ISO / CE / EH&S requirements related to equipment / process development, ensuring robust validation and qualification.

If you meet the Key Skills and Experience, and feel you are a good fit for this role, please apply today!