Quality and Compliance Officer - Askeaton
at Kingspan
Eas Géitine, County Limerick, Ireland -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 18 Feb, 2025 | Not Specified | 19 Nov, 2024 | N/A | Good communication skills | No | No |
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Description:
You will be responsible for the Quality Assurance and Product Compliance within the site. This position is 39 hours per week, and based at our Aeroboard Ltd site in Askeaton, Co.Limerick.
WHY JOIN KINGSPAN AEROBORD?
Kingspan Aerobord is a leading manufacturer of EPS products, supplying a range of industries including insulation for the construction industry and packaging for a variety of blue chip manufacturing companies.
We pride ourselves in building long-term partnerships with our clients to design, manufacture and deliver innovative solutions that help them meet the ever-changing demands of their respective marketplaces.
We are a visionary company with a well-established, supportive team which takes enormous satisfaction in the quality of our work and relationships.
Do you have the skills we are looking for? If so, click ‘apply’ now to be considered as our Quality and Compliance Officer
Responsibilities:
- Management of the sites current and future Integrated Management Systems (ISO 9001 and ISO 37301), and the sites Complementary Management Systems (BRCGS).
- Management representative for all external audits
- Co-ordinate the development of the MS program
- Performing direct quality assurance testing of products to Irish Ágrement Bord and relevant EN standards.
- Preparing for the issue and updating of Product CE DoP’s and Product Specification Sheets.
- Responsibility for the performance of all statutory compliance checks and inspections.
- IMS and CMS Internal Audits.
- Manage company quality and compliance improvement schemes.
- Identify, device and implement relevant changes to SOPs where required.
- Identify, manage and report on quality and compliance key performance indicators.
- Partake in the Single Event Analysis (SEA) and corrective action process.
- Create OPL’s and training documents.
- Delivery of internal training session on quality or compliance related topics.
- Offer suggestions to changes in production methods/equipment for improvements to the quality of the product.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Production / Maintenance / Quality
Clinical Pharmacy
Graduate
Proficient
1
Eas Géitine, County Limerick, Ireland