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Wexford Quality Jobs

Quality Jobs in wexford

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Supervision of the development, maintenance, and distribution of quality documents within the Quality Management System, Design and implementing quality systems improvements. 3rd Degree in technical, science or quality area - Our client is a highly respected and established medical devices company in the South East.

The Quality Engineer will primarily be responsible for maintaining and improving where necessary all quality systems and monitoring production process for compliance to implemented process controls. Engineering or science degree preferably with Quality Engineering included. Ensure continued compliance with all Regulatory Standards.

The New Product & Process Introduction Quality Engineer will primarily be responsible for maintaining and improving where necessary all quality systems and monitoring production process for compliance to implemented process controls for product and process projects

Exciting opportunity for experienced Quality Engineer to take up challenging role with leading manufacturer in Waterford. To ensure quality and technical standards are in place and in use ensuring product and service consistently meets customers’ requirements.

This Quality reliability managers position will be focused on quality process management & improvement geared towards Hygiene & finished product safety for a large manufacturing site in the south-east of Ireland. This role involves the implementation and maintenance of a Quality Reliability Regime throughout the organisation.

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To ensure the development and implementation of the quality management system, ISO 9001:2015. Oversee all elements of the Quality Management System including non-conformances, corrective actions, investigations and root cause analysis. Ensure the effective resolution of above quality issues through relevant processes.

The QA/RA Supervisor is responsible for the supervision of development, maintenance, and distribution of quality documents within the Quality Management System . Supervision of the development, maintenance, and distribution of quality documents within the Quality Management System . FDA Quality System Regulation 21 CFR 820 (QSR)

The regulatory affairs specialist will primarily be responsible for ensuring compliance to all relevant regulations which includes the maintaining all quality systems and related documentation. FDA Quality System Regulation 21 CFR 820 (QSR) ISO13485 Medical Device Quality Management System

  • Negotiable
  • Updated 20/10/2017
  • Wexford

Adheres to Company values and all safety and quality requirements including, but not limited to: Quality Management Systems (QMS), Environmental Management Systems (EMS), (FDA) regulations, Company policies and procedure, and other regulatory requirements.

  • 25000 - 35000
  • Updated 13/10/2017
  • Wexford

This organisation is going through massive growth currently and they are looking for an ambitious Quality Engineer to join their team on a full time basis with a great emphasis on loyalty and progression within the company as there is currently a very low turnover rate within the organisation.

As the Quality Engineer you will work for our client, a Medical Device company. As a Quality Engineer you will develop, improve and monitor the quality management systems to ensure the highest levels of product quality, operational excellence and customer satisfaction while maintaining regulatory compliance.

Due to tremendous developments on this site in recent years, our client, a major global player in their industry globally are looking to recruit a Quality Process Improvement Manager to oversee optimisation of all plant processes with a major focus on Environmental and Quality process standards.

Perform quality inspection, sampling and quality control testing against approved specifications on incoming, in process and finished products. Purpose of the Job - Key Responsibilities

Participate in Supplier audits along with Supplier Quality team. Effectively resolve supplier quality and corrective actions through to SCAR resolution. Work with Supplier Quality in managing product qualification and First Article.

Adheres to Integer Values and all safety and quality requirements including, but not limited to: Quality Management Systems (QMS), Environmental Management Systems (EMS), (FDA) regulations, Company policies and procedure, and other regulatory requirements.

Lead & co-ordinate the day-to-day activities of the operations team (including key support department team members) to meet production targets for customer delivery, product quality & cost ensuring a safe work environment at all times. Liaising with tool room, maintenance, production and quality on a daily basis.

Adhere to company Values, including all safety and quality requirements - Ensures full utilization and accuracy of data systems in the Production, Quality Systems and business analysis process.

  • Negotiable
  • Updated 19/10/2017
  • Wexford

The successful candidate will provide engineering support to production through improved methods, processes, jigs and fixtures, tooling and machine enhancements to improve standard times and employee efficiencies in order to manufacture quality medical guide-wires at the target costs.

Organisational skills and commitment to the delivery of a high quality end product to the client - Co-ordinate the planning and production of the financial statements preparation process in conjunction with the onshore team. Job Description - Sample review financial statement and underlying files. Ensure completeness of disclosure in financial statements.

The mission of Beacon Hospital is to provide exceptional patient care in an environment where quality, respect, caring and compassion are at the centre of all we do. The identification of quality, policy & guideline issues.

Plant handover/hand-back procedures must be followed & all work carried out must be completed, such that it presents zero risk to product quality and personal safety - Experience operating within, and delivering on, the highest quality standards in the manufacturing sector.

Plant handover/hand-back procedures must be followed & all work carried out must be completed, such that it presents zero risk to product quality and personal safety - Experience operating within, and delivering on, the highest quality standards in the manufacturing sector

Work with the Quality Governance Manager to agree the annual monitoring schedule using risk-based methodologies; Keep under review and suggest improvements to the First Line of Defence quality assurance question sets in response to emerging risks, regulatory change, changes in business strategy and common themes/findings;

As an Area Manager you are fully responsible for driving sales in a given number of sites through ensuring exceptional store standards, full availability, product quality and freshness, and customer service. My client is currently seeking an Area Manager to join their rapidly growing business.

Lead or participate in projects, working closely with Production, Maintenance and Quality departments. An exciting opportunity has arisen with our client based in the South East for a Manufacturing Engineer. This is an excellent opportunity to join a progressive organisation - The Role

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