Role and Responsibilities
Communicate and participate in system and process troubleshooting with support team and external agents.
Investigation of factory 4.0/IoT and its live implementation to the current process environment.
Process validation for new products and processes.
Validation, appraisal and support machining and raw materials suppliers.
CNC operations and programming.
Ensure GMP and system safety.
Conduct gauge R&R studies for new product and processes.
Ensure quality of current processes by reviewing and improving on SOP guidelines.
Application and development of statistical tools for use in driving continuous improvement projects.
Lead process improvements initiatives.
Participate in team meetings on timeline projects.
Support capital acquisition activity including: Specifying equipment, contract negotiation, installation and validation.
Interface with materials science, design and quality assurance departments provide our customers with a quality product in a timely manner.
Level 7 degree in Mechanical/Biomed Engineering or equivalent.
Proficient in CAD/Word.
Project management experience.
Strong communication skills.
Motivated, driven and a team player.
Business understanding of operations and there impacts.
Experience in Autodesk Inventor.
Experience in Six Sigma and Lean Manufacturing.
Ability to work effectively work cross functionally.
Tasks and responsibilities will vary with all positions and the scope of each role may not be limited to the contents listed on this job description. The employee’s manager is responsible for communicating any changes deemed necessary to the quality department. It is the employee’s responsibility to adhere to company procedures and GMP in Croom Precision Medical as part of their job description.
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