Responsibilities:
- Provide technical leadership on product and process issues, driving improvements through the team’s VIP programme.
- Lead structured process improvement initiatives across people, service, quality and cost.
- Drive Lean initiatives and support continuous improvement across the operation.
- Partner with Quality and Engineering teams, both within the plant and across the wider corporation.
- Support new product introduction through phase reviews and NPE meetings.
- Provide ongoing manufacturing support to deliver quality, output and cost targets.
- Maintain an accurate capacity model with the Line Supervisor and plan capital requirements in advance.
- Lead project planning and execution for major projects, product/process transfers and capacity or sustaining programmes.
- Develop and maintain GMP-compliant technical documentation in collaboration with the wider team.
- Evaluate new equipment, processes and chemicals with EHS to minimise environmental impact.
- Minimum 2 years’ relevant engineering experience, ideally within the Medical Device industry or another highly regulated environment.
- Experience in equipment installation and qualification.
- Hands-on experience with process validation, including OQ/PQ.
- Strong technical, communication and teamwork skills, with the initiative to drive improvements.
- Working knowledge of MES, SAP and Windchill is advantageous.
- Experience with Fast Track or Full Track Windchill Change Notice (CN) processes is beneficial.
- Project management experience is desirable.
- Experience with Watchman products and processes is an advantage.
emma.barry@collinsmcnicholas.ie
091 706719
