Our Cork based client are now hiring for a Manufacturing Engineer (Hybrid) to join their team. An excellent opportunity to work with a leading Medical Device/Pharma company offering great career progression opportunities. The successful candidate will provide daily support and work on projects, NPI, processes, materials, and equipment in order to achieve launch of new Pharma product - develop and implement new manufacturing processes - improvement projects, liaising with suppliers on materials and working with the latest technologies and equipment.
Responsibilities
Analyse processes, product, material or equipment specifications and performance requirements.
Process and Equipment Validation - IQOQPQ
Responsible for the introduction/transfer and validation of new equipment.
Troubleshoots new products / process working closely with product development.
Continuous Improvement & Yield Analysis.
Continually seeks to drive / improvements in process design, layout and operational performance.
Engaging with technicians, operators, and other cross-functional teams to ensure business process success.
Contribution in NPI (New Product Introduction) development
Execute new equipment introductions and carry out validations.
Root cause analysis using Lean tools and techniques.
Writing and improving process procedures.
PCA (Process Change Analysis) From Documentation to Implementation
Demonstrates good working knowledge and application of validation techniques and associated regulatory requirements.
Qualifications and Experience
NFQ Level 8 in a Technical Discipline (Science, Biomedical, Mechanical, Manufacturing, etc.)
Minimum 2-5 years’ experience working at an Engineering level, ideally in Pharma or Medical Device industry or other highly regulated environment desirable.
Automated Manufacturing equipment experience advantageous but not essential
Process & Equipment validations IQ/OQ/PQ desirable
For more details please contact Gary Keane
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