Our client, a leading medical device company in Galway are currently looking to recruit a Manufacturing Engineer for their site on 12 month rolling contract working on exciting projects!
- Develop and implement manufacturing business improvement projects and processes in order to achieve production goals (i.e., quality, delivery, cost, productivity, and safety) for the production Unit. Support teams to make improvements to existing products and manufacturing processes. Lead projects independently with minimal supervision.
- Assesses process capabilities, prioritizes process improvement opportunities, and innovates and implements process improvements on commercial products.
- Must comply with requirements of the site Environmental, Health and Safety standards and follow procedures and instructions related to these standards.
- Applies technical knowledge to innovate, design, and develop processes, procedures, tooling and/or automation.
- Under guidance, demonstrates proficiency in Project Management (Project Charter, Gantt) tools to maximise project opportunities and to influence and inform key customers and stakeholders.
- Create and utilize Risk Register and System FMEA to identify and remove business and technical risks. Plans, organizes, and conducts all aspects of technical reviews.
- Create E&AS documentation to support new and improved manufacturing processes with validation methods for inspection for verification and process controls.
- Coordinates with the suppliers and external resources needed in developing and implementing new process/product plans
- 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.
- Cultivates a wide range of internal business relationships and begins to develop an external network of resources to facilitate completion of tasks.
- Evaluates in conjunction with EHS new equipment/processes/chemicals for environmental impact/effect to eliminate or lessen such impacts/effects.
- Gives technical guidance to ME I, 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.
- Executes the functional deliverables associated with the CAPA, VIP, Strategic Initiative, and Quality Systems.
- Ensures proper documentation is completed to meet quality systems requirements. (e.g., BOM’s, Routers, FMEA’s, etc.).
Minimum Education and Experience:
- HETAC Level 8 in a Technical Discipline (Science, Biomedical, Mechanical, Manufacturing, etc.)
- Minimum 2-3 years’ experience ideally in Medical Device industry or other highly regulated environment
- Line Support Exp required
For further information on this Contract Manufacturing Engineer role in Galway please contact Anna McGowan on 0864667369 / email@example.com
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