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Quality Technician II (Evenings), Spiddal
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Client:
Location:
Job Category:
Other
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EU work permit required:
Yes
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Job Reference:
fccbe4c088d3
Job Views:
5
Posted:
03.06.2025
Expiry Date:
18.07.2025
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Job Description:
Empowering people, creating technology.
Responsibilities:
* Make product dispositions as and when required. Update documentation such as specifications and visual standards to better define the quality characteristic being dispositioned.
* Prepare and update documentation such as Work Instructions, Product Routings (CHR’s), Visual Standards etc. as required.
* Prepare Engineering Change Orders (ECO’s). Obtain the necessary approvals and where necessary implement on the document control system.
* Perform inspections on product (incoming, in-process and final) as required. This may arise due to product quality investigations, incoming inspection capacity etc.
* Prepare process data such as yield, output rates, No. of NCR’s etc.
* Perform First Article Inspections as required.
* Raise Non-Conformance Reports and ensure associated product is segregated, oversee that NCR’s are closed out in a timely manner.
* Oversee the execution of validation activity as required.
* Carry out scheduled audits (Internal, Standard Work, out of the box etc.)
* Adhere to Plant Safety requirements and Health & Safety requirements relating to your work, assuming responsibility for those aspects of the OH&S System over which you have control to ensure the health and safety of yourself and others.
* Be aware of the potential environmental impacts associated with your work and the implications of non-conformance.
* Contribute to enhanced energy performance by conservation of energy where possible (Lighting, Equipment, Air Conditioning etc).
* Contribute to the continual improvement activities of the OH&S, Environmental and Energy Management systems through participation, providing feedback/ suggestions for improvement and by reporting accidents, dangerous occurrence, near miss/ illness, good catch and environmental incidents in a timely manner.
* To take on other duties which the Company may assign you from time to time. These ‘other duties’ will be agreed with Management prior to any assignment.
Qualifications:
* Diploma qualification Quality or a related discipline Or significant relevant experience in a quality assurance role within the Medical Device Industry.
* A minimum of 3 years’ experience in a similar Quality related role in the Medical Device / Components industry.
* Thorough knowledge of Freudenberg Medical products and processes.
* Must be able to make product dispositions decisions.
* Excellent attention to detail.
* Good communication skills both verbal and written.
* A positive attitude in dealing with people.
* Ability to learn and adapt to various situations.
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