Responsibilities:

• Oversee the progression of new designs throughout the product lifecycle to ensure a smooth transition to large-scale manufacturing.
• Lead initiatives for product and process enhancements in collaboration with the team, aiming for continuous improvement.
• Foster close partnerships with Subject Matter Experts to ensure alignment of new products with existing manufacturing capabilities.
• Develop expertise in specialized processes to optimize manufacturing efficiency and quality.
• Guarantee adherence to world-class manufacturing standards by coordinating with TEOA and operations teams.
• Introduce efficient manufacturing processes for new products, focusing on boosting productivity while maintaining quality standards.
• Conduct comprehensive validations before process handover to manufacturing to ensure reliability and compliance.
• Implement innovative technical solutions to address manufacturing challenges effectively.
• Maintain high compliance standards with Medical Devices manufacturing requirements, including ISO and FDA regulations.
• Identify and implement Lean principles to enhance yield, throughput, and overall productivity.
• Explore new process technologies to gain a competitive advantage in the industry.
• Manage relationships with technology providers and suppliers to ensure seamless integration of new processes.
• Ensure compliance with Health, Safety, and Environmental requirements in all manufacturing processes.

What Your Background Should Look Like:

• Bachelor's degree in Engineering or equivalent, with at least 2 years of relevant experience.
• Strong technical background with experience in new product introduction preferred.
• Self-motivated individual with strong decision-making abilities.
• Knowledge of ISO and FDA compliance, particularly in validation processes.
• Proficiency in six sigma and lean manufacturing principles.
• Excellent communication, planning, and organizational skills.
• Problem-solving abilities with a focus on innovative and cost-effective solutions.
• Computer literacy, preferably with experience in 3D modeling and Cagila software.
• Proven track record of excellent timekeeping and attendance.

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

For further information on this please contact Johanne Kennedy on 0864403725/ choices@hero.ie

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 your data. We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel.