What We Do:

Crest Solutions are an engineering and software company that supply and support the resourcing of engineers, analysts, specialists and other professionals in this field. We are home to a vibrant group of professionals, working together to deliver to our clients. As a Gold Certificated company in the NSAI Excellence Through People scheme, Crest Solutions strives to guide many of Ireland’s most successful organisations to become more efficient, productive, flexible, competitive and innovative, through the development of great people.

Responsibilities and Tasks:

• Provide daily support of products, processes, materials, and equipment in order to achieve production goals (i.e., quality, delivery, cost, productivity, and safety).
• Develop and implement manufacturing business improvement projects and processes for disposable medical devices. Support teams to make improvements to existing devices and manufacturing processes. Lead less complex projects independently with minimal supervision.
• Analyse 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.
• Summarize, analyse, and draw conclusions from test results leading to effective technical resolution.
• Troubleshoot new products / process working closely with product development.
• Continually seek to drive / improvements in process design, layout and operational performance.
• Demonstrate good working knowledge and application of validation techniques and associated regulatory requirements.
• Actively promote 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.
• Give technical guidance to Associate Engineers and technicians.
• Become 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.
• Understand and comply with all the regulations governing the quality systems.
• Ensure 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.

Skills and Experience:

• NFQ Level 8 in a Technical Discipline (Science, Biomedical, Mechanical, Manufacturing, etc.)
• Minimum 3-5 years’ experience working at an Engineering level, ideally in Medical Device industry or other highly regulated environment
• Project Management experience is desirable