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Westmeath Quality Jobs

Quality Jobs in westmeath

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the Midlands region in the recruitment of Quality Engineer. Work alongside production teams to find process improvements to deal with quality issues. Guide quality audits from governing bodies and customers. Engage with production teams to find process improvements to deal with quality issues.

Due to continued expansion of their operations our client a well-established Multinational Healthcare Manufacturer now require a qualified and experienced Quality Project Engineer.

Quality Assurance NPI Eng - Medical Device - Key role of this position is to proactively support quality engineering activities with regards to the Quality Management System, product robustness changes & compliance related projects, ensuring technical correctness, & compliance with requirements of global regulations.

Vickerstock are continuing to work closely with our client in the food manufacturing and production sector for the recruitment of a Quality Systems Technician

Senior Quality Engineer – Strategic Projects

Teleflex Medical Europe

3 company reviews

We pride ourselves on being totally Customer Centric in our unrelenting focus on Quality, Service and Value as perceived by our customers. This role is an integral part of a team with responsibility for executing these projects in line with our values without compromise on Quality of products or customer’s needs.

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Quality Systems Engineer

Abbott Ireland

19 company reviews

The Quality Systems Engineer will be part of the Engineering Team reporting to the Technical Engineering Manager. Responsible for the tracking and timely closeout of all Engineering related exception reports on the Quality Management System. Support the CAPA and Quality Metrics programme as required.

QC Lab Support Validation Engineer position available in Westmeath now, please see below for further information.

My Client, a world leader in medical technology are seeking to recruit a Quality Engineer to join their team on a 12 month contract.

We are seeking an experienced, dedicated Quality Control Technician to join our team. In this position, you will maintain quality standards by approving incoming materials, in-process production, finished products, and recording the results.

Management/Assistance with product quality review - Are you a recently qualified QP who is looking to get onto a company license? Or perhaps you are an experienced QP looking to move West and work in a cross functional environment with responsibility for QMS. What you need to know - Your new job - Responsibility for daily batch release

Senior MDR Quality Systems Specialist, QA / RA

Teleflex Medical Europe

3 company reviews

Improve and maintain the quality management system (QMS) in line with the Medical Device Regulation (MDR) and ISO13485, ISO9001, 21CFR 820. Teleflex Medical Job Title: Senior MDR Quality Systems Specialist/MDR Quality Systems Specialist Quality system compliance to ISO 13485, ISO 9001, 21CFR 820 and EU MDR - Proactive in the achievement of high quality standards

Matrix Recruitment is working closely with our client in the Medical Device Sector in Co. Galway in the recruitment of a Quality Assurance Engineer. You will be responsible for providing quality support to processes, materials and products to client standards and relevant regulatory standards.

You will report to the RA Manager and provide support to the Regulatory Affairs Department and improve resourcefulness and maintain a high standard of quality to the company’s products. What you need to know

Our client, a midlands based medical devices company are recruiting for a Regulatory Affairs Specialist for their site in Offaly.

Demonstrate a commitment to patient safety and product quality. Implements policies and procedures to maintain compliance to standards and quality systems - Review of Batch records from a Quality Control perspective. Opportunity for an experienced Lab Supervisor seeking to develop their career with a global pharmaceutical company. The Opportunity

As a Vendor you will need to ensure that suppliers continually develop their quality and technical processes in line with the customer requirements. Support Senior Management responsible for delivering all aspects of the Supplier Quality Assurance function.

Strong leadership qualities R&D Client in Co. Offaly is keen to recruit a Software Manager with experience managing Java development projects & teams. Degree in an IT related discipline such as Software Engineering, Computer Science or Software Development - Several years experience as a hands-on Java developer - Strong design architecture experience

Snr Validation Supervisor

Medtronic

21 company reviews

By providing quality care at the lowest possible cost, we will succeed as a company, and take the future of healthcare Further, Together. At our Quality function in Medtronic, plc, we focus on supporting systems that ensure we provide high quality products to our customers.

Team Lead, Analytical Labs, PPD Athlone

PPD Pharmaceutical Product Development

4 company reviews

Our lab employees are committed to quality results and strict compliance with regulatory standards.

A business partner Finance Manager job in Athlone, with real influence and responsibility over global quality in a thriving multinational organisation that offers excellent career progression opportunities. Based in Athlone, Co Westmeath, you will become the Finance Manager of Global Quality for this $1.8bn multinational.

Works with manufacturing and quality colleagues as part of an Operations team whose shared goal is to realise the safety, quality, delivery and cost objectives of the site. Is always prepared to escalate any safety, quality or performance risk observed.

Have an in-depth knowledge of Good Manufacturing Practice (GMP), Quality System Regulations and ISO quality standards. As Head of Validation - your main duties and responsibilities will include; Process, Software, Equipment, Utilities & Facilities Validation activities.

Assures quality of business systems by developing and executing test specifications, and implementing test and quality plans, while working with quality assurance analysts to improve IT quality processes. Creates and provides quality training material for user assistance and system usage.

Works with manufacturing and quality colleagues as part of an Operations team whose shared goal is to realise the safety, quality, delivery and cost objectives of the site. Prioritises training needs based on safety first followed by quality and then delivery (process, equipment, systems of work).

You should possess an in-depth knowledge of Good Manufacturing Practice (GMP), Quality System Regulations and ISO quality standards. Head of Validation for a Medical Devices company based in Athlone - A Head of Validation is required by CareerWise Recruitment for our Athlone based client.

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