Manufacturing Engineer - (Hybrid)

CREGG; Cork; Hybrid; EUR 50,000 - 70,000; Full time

Job summary

A leading recruitment agency is seeking a Manufacturing Engineer (Hybrid) for a Cork-based client in the Medical Device/Pharma sector. The role involves supporting project launches, developing new manufacturing processes, and engaging with cross-functional teams. Candidates must have an NFQ Level 8 in a technical discipline and 2-5 years' experience in a regulated environment, ideally in Pharma or Medical Devices.

Qualifications

• Minimum 2-5 years’ experience working at an Engineering level in Pharma or Medical Device industry.
• Proven experience in Project Planning/Management.
• Familiarity with Process & Equipment validations IQ/OQ/PQ is desirable.

Responsibilities

• Analyse processes, product, material or equipment specifications.
• Responsible for the introduction/transfer and validation of new equipment.
• Engaging with technicians, operators, and cross-functional teams.
• Conduct root cause analysis using Lean tools.

Skills

Process and Equipment Validation

Continuous Improvement

Root Cause Analysis

Project Planning/Management

Education

NFQ Level 8 in a Technical Discipline

Tools

Lean tools

Automated Manufacturing equipment

Job description

Manufacturing Engineer – Cork (Hybrid)

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.

About the role

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.
• Project Planning/Management experience highly desirable.
• Automated Manufacturing equipment experience advantageous but not essential
• Process & Equipment validations IQ/OQ/PQ desirable

For more details please contact Gary Keane

[e-mail]

086-1030418 / 091-700814