CREGG Recruitment are hiring for an Equipment Test Engineer, the role will involve the maintenance, build and testing of large electrical testing equipment for medical device manufacturing.
The successful candidate can come from Electrical engineering, Electrical Technician or very strong electrical background.
The role will involve, assembly, checkout and validation of the next generation functional test systems used to fully test Electronic Implantable Defibrillator and Pacemaker devices from PCBA Level to Finished goods.
These Test systems comprise of National Instruments PXI cards along with in-house designed fixtures to test the Implantable medical devices to ensure they meet full design requirements. The Role will involve building the system according to the design document and specification and then performing a full checkout and validation of the system to release to the production floor.

EXPERIENCE:

The ideal candidate should have experience and knowledge in using National Instruments cards, systems and software. An ability to build and assemble complex fixturing and following schematics is required. Must have excellent knowledge in electronics with proven problem-solving abilities and the ability to project manage issues to closure. Knowledge of test software applications such as Lab View and C or C++ and experience in validations in the medical device industry would be an advantage.

QUALIFICATIONS:

Level 8 technical qualification in electrical or electronic engineering or related discipline. Greater than 5 year’s relevant experience in a related environment.

• Ability to work on own initiative and meet tight deadlines and project plan.
• Perform the physical assembly and checkout of Test systems and Fixturing following system schematics and documentation.
• Using knowledge of standard test software applications such as Labview and C C++, able to work with in-house and external software developers and system engineers to define and drive improvements and solve problems with the test systems and software applications.
• Performs tests, analyzes data, writes reports and executes validations to medical device standards.
• Excellent data analysis and technical problem-solving skills, utilizing common applications and in-house component and device tracking systems to assist in the building and checkout of production systems.
• Utilizing good documentation skills complete regulatory submissions using change notice process and procedures.
• Work with quality, manufacturing engineering EHS and operations, providing improvement feedback and assisting with resolution of quality and manufacturing issues and the implementation of the completed systems to the production floor.