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Our medical device client is looking for the ideal candidate to be responsible for the management, direction and coordination of all quality and regulatory activities for the site. Ensure department targets and objectives are met – safety, quality, , complaint analysis, product conformances;
Our client, a medical device company in Offaly are currently looking to recruit a Quality Engineer for their site. You will have key responsibility for coordination of plant projects, sustaining materials, OPEX (Continuous improvement and costs reduction), Compliance and Quality related projects.
Our client, a Multi-National Medical Devices manufacturer is seeking an experienced NPI Quality Engineer to join their dynamic team on a permanent basis. Providing Quality support to processes, materials, and products.
The Technical Quality Manager is a vital role heading up Food Safety and Quality for the Green Isle pastry production facility at Portumna. We pride ourselves on delivering great quality tasty food and innovative food solutions, making meals times easier for consumers.
Improve and Maintain the quality management system (QMS) in line with ISO13485, ISO9001, 21CFR 820 and Medical Devices Directive. Teleflex Medical Job Title: Quality Systems Specialist Quality system compliance to ISO 13485, ISO 9001, 21CFR 820 and Medical Devices Directive - Support QSRB (Quality System Review Processes) & MRB (Material Review Board) processes
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Circa 10 years' manufacturing experience working in a quality assurance role or related department desired. Our client seeks a Quality Manager to provide leadership and maintain Quality to a world class standard.
My client are currently recruiting a Quality Engineer for their facility in the midlands. Reporting to the Quality Manager, the successful candidate will be responsible for initiating, recommending, verifying and providing solutions for quality issues.
Matrix Recruitment is working closely with their Client a Medical Device company in Co. Offaly in the recruitment of a Quality Technician. This is a permanent position and you will report to the Site Quality Manager. A 3rd level qualification in science, quality or related discipline - What you need to know - Salary €28KYour new job
Matrix Recruitment is working closely with our Healthcare Company in Co. Offaly in the recruitment of a Quality Manager. Ensure achievement of recognised quality standards (ISO/FDA) and legal compliance. Monitor quality data daily, and take appropriate action.
Matrix Recruitment is working closely with our Healthcare Company in Co. Offaly in the recruitment of a Quality Engineer. Manage / execute site quality systems including CAPA, internal and supplier auditing, product release and validation activities. Third level qualification in Engineering/Science/Quality or related discipline.
The Supplier Quality Data Analyst develops, implements, and maintains supplier databases and collects and analyzes supplier quality data in preparation for generation of statistical and analytical reports
Matrix Recruitment is working closely with our Medical Devices Company in Co Offaly in the recruitment of a Junior Quality Engineer. What you need to know - This is a Permanent position. Your new job - Development of Validation Protocols, generation of validation reports and record keeping.
We continuously seek new and innovative ways to produce top quality From this supply network of quality pig meat, This position will report to the Quality Assurance Manager. Monitor carcases quality Quality focus with a drive to ensure standards are upheld - Lab Technician - Rosderra Irish Meats Group is the largest pork - processing company in Ireland.
Document control including RFI management, submittal, transmittals, purchasing management, quality plan implementation, drawing management, final handover packs development & providing engineering support for the project team when and as required. Attend quality meetings and participate in QA/QC walk downs when required
This is a permanent position with excellent opportunities and you will have responsibility for the daily production operation ensuring the product is manufactured to the highest quality that meets regulatory requirements. Ensure all operational performance targets are reached including productivity, wastage, quality and safety
Communicate with suppliers, strategic sourcing, quality and regulatory affairs in the design of new products - Work with quality and R&D personnel to lead investigation into product complaints, determine root cause and implement corrective actions - You will work as a R&D Engineer and will work for our medical device client based in Co. Westmeath.
The NPI QA Engineer will be responsible for providing Quality support to processes, materials, and products. Assuring Quality standards are maintained and assist with the implementation of and compliance to the Quality Management program and for Supporting company goals, objectives, policies, procedures, quality systems, and FDA regulations.
Interface with suppliers, Strategic Sourcing, Quality and Regulatory Affairs in the design of new or redesign of existing products to meet user needs. As requested, work with Quality and R&D personnel to lead investigation of product complaints of new products to determine root cause and implement corrective action.
Write test method and validation protocols, SOPs, and other quality system documentation to allow the execution of the analysis in a GMP environment. Participate in Quality and Safety regulatory audits.
• Work with manufacturing, Quality and outside vendors to schedule servicing, calibration and validation work on equipment and utilities. • Participate in Quality and Safety regulatory audits as required and input to similar supplier audits. Minimum 5 years' experience in pharmaceutical/healthcare industry.
• Write test method and validation protocols, SOPs, and other quality system documentation to allow the execution of the analysis in a GMP environment. • Participate in Quality and Safety regulatory audits. To support the development, optimisation, and validation of analytical test methods either in-house or in collaboration with external service providers
Support writing of batch manufacturing records, SOPs and other quality documentation - What you need to know - My client is looking for Process Scientist to join their team. As Process Scientist, you will work with a biopharmaceutical company in the Midlands, within a growing team in the validation of methods for NPI projects.
• Support the writing of Batch Manufacturing Records, SOPs, and other quality system documentation required for GMP manufacture • Participate in Quality and Safety regulatory audits - The successful candidate will have responsibility for the development and validation of processes for recombinant antibodies for veterinary use.