Cregg Recruitment is actively looking for a Product Builder to join a well-renowned medical device company in Galway city.
Midweek Monday – Friday role, a permanent role, with a view to career progression internally.
Overall Job Objectives
- The purpose of this job function is to engage in the day-to-day manufacturing of medical devices.
- The Senior Product Builder will work as part of the Operations Team in the development and manufacture of innovative medical devices in accordance with the requirements of International Standards
Main Duties and Responsibilities
- Build sub-assemblies and finished devices including packaging activities for testing, clinical investigations, and commercial release.
- Complete part and subassembly visual and dimensional inspection activities in line with documented procedures and standards.
- Responsible for issuing materials to the manufacturing line, and setting up equipment & fixtures on the manufacturing line.
- Assist with the management of the Material Control System including incoming inspections, part issuance, and tracking.
- Participate in training activities and become proficient in the required manufacturing and inspection activities in a timely manner.
- Assist in the preparation and execution of “in process” device testing and recording of associated results.
- Identify and communicate opportunities for improvement in product quality and throughput and participate in the successful implementation of the same.
- Where required provide training and guidance to team members on building, inspection, and testing of the product.
- Maintain compliance with released Work Instructions and Procedures.
- Complete written and soft-copy quality records in line with GDP requirements.
- Be dependable in coming to work, adhering to work and break schedules and meeting required quality and productivity standards.
Qualification Required
- Leaving Certificate or equivalent minimum.
- The third-level academic qualification will be advantageous.
Work Experience or Training Required
- Minimum of 2 years of medical device manufacturing experience (at least 2 years cleanroom-based) or equivalent.
- Demonstrated experience with GDP & GMP standards is advantageous.
Special Skills Required
- Must have good communication skills.
- Must be able to work well in a team environment.
- Ability to perform a variety of tasks requiring dexterity and fine motor skills.
- Demonstrate a high level of initiative.
- Excellent attention to detail.
- Effective contributor with a light level of supervision.
- Proficient in the use of desktop software e.g. excel, word – computer literacy will be advantageous
Cregg Recruitment is actively looking for a Product Builder to join a well-renowned medical device company in Galway city.
Midweek Monday – Friday role, a permanent role, with a view to career progression internally.
Overall Job Objectives
- The purpose of this job function is to engage in the day-to-day manufacturing of medical devices.
- The Senior Product Builder will work as part of the Operations Team in the development and manufacture of innovative medical devices in accordance with the requirements of International Standards
Main Duties and Responsibilities
- Build sub-assemblies and finished devices including packaging activities for testing, clinical investigations, and commercial release.
- Complete part and subassembly visual and dimensional inspection activities in line with documented procedures and standards.
- Responsible for issuing materials to the manufacturing line, and setting up equipment & fixtures on the manufacturing line.
- Assist with the management of the Material Control System including incoming inspections, part issuance, and tracking.
- Participate in training activities and become proficient in the required manufacturing and inspection activities in a timely manner.
- Assist in the preparation and execution of “in process” device testing and recording of associated results.
- Identify and communicate opportunities for improvement in product quality and throughput and participate in the successful implementation of the same.
- Where required provide training and guidance to team members on building, inspection, and testing of the product.
- Maintain compliance with released Work Instructions and Procedures.
- Complete written and soft-copy quality records in line with GDP requirements.
- Be dependable in coming to work, adhering to work and break schedules and meeting required quality and productivity standards.
Qualification Required
- Leaving Certificate or equivalent minimum.
- The third-level academic qualification will be advantageous.
Work Experience or Training Required
- Minimum of 2 years of medical device manufacturing experience (at least 2 years cleanroom-based) or equivalent.
- Demonstrated experience with GDP & GMP standards is advantageous.
Special Skills Required
- Must have good communication skills.
- Must be able to work well in a team environment.
- Ability to perform a variety of tasks requiring dexterity and fine motor skills.
- Demonstrate a high level of initiative.
- Excellent attention to detail.
- Effective contributor with a light level of supervision.
- Proficient in the use of desktop software e.g. excel, word – computer literacy will be advantageous