Manufacturing Project Engineer – Clonmel

CREGG; Tipperary; On-site; EUR 40,000 - 60,000; Full time

Job summary

A multi-national medical device company is seeking a Manufacturing Project Engineer based in Clonmel, Tipperary. The role involves overseeing the introduction and validation of new equipment, conducting validations, and collaborating with cross-functional teams. The ideal candidate should hold a Level 8 engineering degree and possess 2-5 years of manufacturing experience. This position promises a dynamic work environment focused on continuous improvement and patient safety.

Qualifications

• 2-5 years minimum experience in manufacturing, automated experience an advantage.
• Degree into mechanical, manufacturing, or related engineering.

Responsibilities

• Responsible for introduction and validation of new equipment.
• Execute validations: IQ/OQ/PQ protocols.
• Analyse specifications and performance requirements of equipment.

Skills

Manufacturing

Validation

NPI

Quality Engineering

Root Cause Analysis

Education

Level 8 bachelor's degree in related engineering

Job description

Manufacturing Project Engineer – Clonmel

Manufacturing Project Engineer – Tipperary.

Job Title:
Manufacturing Project Engineer
Location:
Clonmel, Tipperary
Industry: Medical Devices
Company information:
A large Multi-National Medical device company, leading for over 40 years
Role Profile

Role suitable for: Manufacturing, validation, NPI and Quality Engineers.

• Responsible for the introduction, qualification / validation of new equipment.
• Executing validations – Protocols – IQ/OQ/PQ
• Analyses process, product, material or equipment specifications and performance requirements.
• Work with cross-functional teams to identify and resolve production/engineering issues.
• Summarises, analyses, and draws conclusions from test results leading to effective technical resolution.
• Transfer and validation of equipment from one clean room to another.
• Continuous Improvement & Yield Analysis.
• Continually seeks to drive / improvements in process equipment 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
• 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.
• Actively promotes 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.
• Gives technical guidance to Associate Engineers and technicians.
• Understands and complies with all the regulations governing the quality systems.
• Ensures 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.

Qualifications / Professional Skills / Knowledge

• Degree required: Level 8 bachelor's related engineering degree: mechanical, manufacturing etc
• Proven experience: 2-5 years minimum experience, automated manufacturing experience an advantage

Contact:
For a confidential discussion or to find out more, please contact:
Gary Keane
Email: [e-mail]
Phone: [phone]