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Contact Info
Claire Kenny
Life Science

+353 1 507 9287
claire.kenny@lifescience.ie
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Details

Manufacturing Engineer


Reference:CK/A005781 Location: Galway City
Qualification:DegreeExperience:2-3 Years
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: Manufacturing Engineer

Manufacturing Engineer
Our client is a medical device company based in Galway. They are currently seeking a Manufacturing Engineer to join their team for a 12 month contract. The role will involve providing support of products, processes, material and equipment to achieve production goals.

Responsibilities:
• Analyses process, product, material or equipment specifications and performance requirements.
• Under broad supervision / guidance compiles and analyses operational, test and experimental data to establish performance standards for newly implemented or modified products / processes.
• Summarises, analyses and draws conclusions from test results leading to effective technical resolution.
• Troubleshoots new products / process working closely with product development.
• Supports purchasing of new equipment.
• Continually seeks to drive / improvements in process design, layout and operational performance.
• Demonstrates good working knowledge and application of validation techniques and associated regulatory requirements.
• Actively promotes and participates in a cross -functional teamwork environment.
• Evaluates in conjunction with EHS new equipment/processes/chemicals for environmental impact/effect to eliminate or lessen such impacts/effects.
• Gives technical guidance to Associate Engineers and technicians.
• Is an influential team member, fully motivated to achieve and demonstrate best practices in line with the department and Site objectives.
• Demonstrate a primary commitment to patient safety and product quality.
• Understands and comply with all the regulations governing the quality systems.
• Ensures all direct reports are aware of their commitment to patient safety and product quality, are current with their training requirements and that they understand and comply with all other regulations governing their work.

Qualifications
• HETAC Level 8 in a Technical Discipline (Science, Biomedical, Mechanical, Manufacturing, etc.)
• Minimum 2-5 years’ experience ideally in Medical Device industry or other highly regulated environment in an Engineering position
• Project Management experience desired
• Experience with plasma processing (surface modification, cleaning, etching) and working knowledge of surface and interface characterisation methods and vacuum technologies highly desirable.

If you would like further Information you can contact the recruiter directly:

Claire Kenny | Tel: +353 (0) 1 507 9287