City. The overall Purpose of this role is to maintain automation
equipment in line with health & safety, operational and quality work
instructions, procedures and policies to ensure the production of
quality product in a timely, safe, efficient and compliant manner.
Key Responsibilities and End Results: (Essential responsibilities
include but are not limited to the following):
* To maintain automation equipment in excellent condition ensuring
consistent quality, output and yield.
* Follow systematic root cause problem solving and troubleshooting to
resolve issues.
* Carry out preventative and corrective maintenance, completing all
associated paperwork and records.
* Lead and implement process improvements to achieve more efficient
operations, while adhering to change management and cGMP requirements.
* Assist with the commissioning of new equipment / projects.
* Order and maintain appropriate stock of spare parts.
* Cross Train technicians as required.
* Flexible to travel to support new equipment buy-offs / training.
* Support all company safety and quality programs and initiatives.
* Ensure ongoing compliance with GMP in all practices, recording of
events and processes.
* Ensure compliance with all learnings from all GMP training events.
* Other responsibilities may be assigned from time to time as needed,
based on the evolution of the company and the requirements of the
department/position.
Skills/Attributes:
* Systematic & structured troubleshooting / problem solving skills.
* Ability to provide innovative solutions to complex technical
problems.
* Adherence to change management procedures and cGMP requirements.
* Good written and oral communication skills.
* Ability to work well in a team environment.
* High level of safe working practices and awareness.
* Computer literate with MS Office skills.
Job Specifications: The minimum education and experience required to
perform this job competently.
* The successful candidate will have Level 6, Level 7 or Level 8 HETAC
qualification in Manufacturing Technology, Mechanical / Automation
Engineering, Electrical, Electronics, Mechatronics or similar.
* Qualified trades personnel with industrial experience will also be
considered. (Electrical must be trade qualified)
* 3 years + experience in high volume automation / robotics required.
* Experience in a Healthcare medical device manufacturing environment
highly desirable.
* Experience in Pneumatics, Electronics, Hydraulics, Programmable
Controllers, Servo Motor drives, Vision systems, Ultrasonic welding,
workshop machining desirable.
* Understanding of Process Capability.
* Understanding of MSA or GR&R.
* Experience in leading process improvement projects in medical device
environment.
* Experience in FAT, SAT, IOPQ of automated assembly lines.
* All applicants must be available to work shift New position in growing medical device company based in Waterford
City. The overall Purpose of this role is to maintain automation
equipment in line with health & safety, operational and quality work
instructions, procedures and policies to ensure the production of
quality product in a timely, safe, efficient and compliant manner.
Key Responsibilities and End Results: (Essential responsibilities
include but are not limited to the following):
* To maintain automation equipment in excellent condition ensuring
consistent quality, output and yield.
* Follow systematic root cause problem solving and troubleshooting to
resolve issues.
* Carry out preventative and corrective maintenance, completing all
associated paperwork and records.
* Lead and implement process improvements to achieve more efficient
operations, while adhering to change management and cGMP requirements.
* Assist with the commissioning of new equipment / projects.
* Order and maintain appropriate stock of spare parts.
* Cross Train technicians as required.
* Flexible to travel to support new equipment buy-offs / training.
* Support all company safety and quality programs and initiatives.
* Ensure ongoing compliance with GMP in all practices, recording of
events and processes.
* Ensure compliance with all learnings from all GMP training events.
* Other responsibilities may be assigned from time to time as needed,
based on the evolution of the company and the requirements of the
department/position.
Skills/Attributes:
* Systematic & structured troubleshooting / problem solving skills.
* Ability to provide innovative solutions to complex technical
problems.
* Adherence to change management procedures and cGMP requirements.
* Good written and oral communication skills.
* Ability to work well in a team environment.
* High level of safe working practices and awareness.
* Computer literate with MS Office skills.
Job Specifications: The minimum education and experience required to
perform this job competently.
* The successful candidate will have Level 6, Level 7 or Level 8 HETAC
qualification in Manufacturing Technology, Mechanical / Automation
Engineering, Electrical, Electronics, Mechatronics or similar.
* Qualified trades personnel with industrial experience will also be
considered. (Electrical must be trade qualified)
* 3 years + experience in high volume automation / robotics required.
* Experience in a Healthcare medical device manufacturing environment
highly desirable.
* Experience in Pneumatics, Electronics, Hydraulics, Programmable
Controllers, Servo Motor drives, Vision systems, Ultrasonic welding,
workshop machining desirable.
* Understanding of Process Capability.
* Understanding of MSA or GR&R.
* Experience in leading process improvement projects in medical device
environment.
* Experience in FAT, SAT, IOPQ of automated assembly lines.
* All applicants must be available to work shift
We need : English (Good)
Type: Permanent
Payment:
Category: Others
