Manufacturing Engineer II

Hero Recruitment; Munster; On-site; EUR 45,000 - 65,000; Full time

Job summary

Join a leading organization in medical device manufacturing as a Manufacturing Engineer II. Drive efficiency, tackle engineering challenges, and contribute to innovative projects in Clonmel, Ireland. This role offers opportunities for advancement in a collaborative and high-quality environment.

Qualifications

• Strong foundation in engineering principles.
• Experience in manufacturing or process engineering roles.
• Equipment Validation Experience.

Responsibilities

• Streamline production operations and address performance issues.
• Lead technical initiatives for process enhancement.
• Prepare reports and communicate findings effectively.

Skills

Problem-solving mindset

Excellent communication skills

Ability to manage tasks independently

Job description

Job Title: Manufacturing Engineer II x3 (Projects)

Location: Clonmel, Ireland

Contract: 12 Months Rolling

Overview

Join a world-leading organisation at the forefront of innovation in medical device manufacturing. As a Manufacturing Engineer II, you’ll drive efficiency and quality within production, tackle complex engineering challenges, and play a pivotal role in integrating cutting-edge processes and products. This is your opportunity to advance your career in a thriving, supportive, and globally recognised company based in the vibrant community of Clonmel, offering an outstanding quality of life amidst Ireland’s scenic beauty and rich heritage.

Key Responsibilities

• Process Optimisation:
• Streamline production operations by monitoring equipment, tools, and processes, addressing performance issues to ensure optimal output, product quality, and cost efficiency.
• Product and Process Development:
• Lead technical initiatives to enhance current processes and drive innovation in next-generation programmes, aligning with strategic goals.
• Problem Solving and Analysis:
• Apply advanced engineering principles to solve complex challenges, develop novel solutions, and drive breakthroughs in manufacturing technology.
• Reporting and Communication:
• Prepare detailed reports, share insights through presentations, and communicate findings effectively with internal stakeholders.
• Leadership and Collaboration:
• Mentor colleagues by sharing technical expertise, guiding project teams, and setting clear goals and objectives for collaborative success.
• Quality Commitment:
• Demonstrate unwavering dedication to product quality and patient safety by adhering to quality system policies and regulatory standards.
• The predominant function for these Engineers will be executing validations on duplicate sets of equipment.

What We’re Looking For

• Experience and Knowledge:
• Strong foundation in engineering principles, concepts, and practices.
• Experience in manufacturing or process engineering roles, preferably within the medical device or regulated industry.
• Working knowledge of industry and business practices.
• Skills and Abilities:
• Problem-solving mindset with the ability to address complex issues and implement effective solutions.
• Excellent communication skills to present ideas and collaborate across teams.
• Capacity to manage tasks independently while contributing to team objectives.
• Equipment Validation Experience.

Ready to Apply?

Take the next step in your career by joining a company committed to excellence, innovation, and making a difference in people’s lives. Apply today and become part of our success story in Clonmel, Ireland!

For further information on this role, please contact Diarmuid Lannon on [phone] or email [e-mail] Check out all our open jobs on our HERO Recruitment website – https://www.hero.ie/

Please Note: Under its obligation under the Data Protection legislation, HERO Recruitment will not forward your details to any company without your prior approval.

Data can only be transferred outside of the EEA on the basis of standards contractual clauses, to a country for whom an adequacy decision has been given by the European Commission or where the express permission of the data subject has been given. You have supplied us with your personal data in the process of applying for a position. Our client company may have personnel outside of the EEA who will review you data. We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel.