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Act as quality point person, providing guidance and feedback on QA issues - Support review and approval of quality control documentation for the release of materials on site - Seeking to recruit a Site QA for leading pharmaceutical multinational based in the Midlands.
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.
Provide quality and cGMP input and oversight for all start-up project activities through commercial readiness for biologics facility. Participate in verification quality risk assessments and provide quality oversight to ensure verification quality risk assessments are effectively maintained/controlled.
At least 5 years' experience in senior quality role, preferably in an automotive or medical device area - The successful candidate will be required to lead and co-ordinate the quality function, to ensure that customer and internal requirements are understood, managed and fulfilled though the direction and co-ordination of the quality management system.
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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the Co Galway region in the recruitment of a Design Assurance Quality Engineer - This is a permanent position and you will report to the Quality Manager - Work closely with R&D, Clinical, Marketing, Process Development, Regulatory and Manufacturing to provide technical and quality systems input to new product designs.
A Medical Device organisation in Galway is seeking a Quality Assurance Engineer to join them and become a key team member to establish, implement and maintain Quality Systems on site. Our client is currently seeking a Quality Assurance Engineer to join a large collaborative team at their facility in Galway.
I require a Quality Engineer to work in Westmeath - The Midlands. My client are a medical device manufacturer and require an experienced Quality Engineer for their site. As Quality Engineer, you will be based in Westmeath in the medical device manufacturing site.
My Client are currently recruiting a Quality Manager for our facility in the midlands. The successful candidate will be responsible for the management, direction and coordination of all quality and regulatory activities for our operations in the plant. Ensure that all products manufactured meet required quality specifications.
Westmeath in the recruitment of a Quality Manager. Ensure that the organization’s Quality Management System conforms to customer, internal, ISO 9001/ISO13485/IATF16949, and regulatory/legal requirements. Direct the day to day activities of the Quality department - Third level degree in engineering or quality related field.
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 their Medical Devices client in Westmeath Region in the recruitment of a Supplier Quality Engineer for their Quality department. This is a permanent position and you will report to the Quality Manager.
the Galway region in the recruitment of Quality Engineer – (Quality Systems / Supplier Quality) Development and application of the BMR quality system as it relates to specified elements of the QMS, including training for compliance to ISO13485 and the FDA Quality System Regulations (QSR).
Matrix Recruitment is working closely with their Medical Devices Client in the Galway / Mayo / Westmeath area in the recruitment of a Senior Quality Engineer for their Quality Assurance department. Improve Quality system requirements. Supervise personnel within an area of the Quality Department. Experience in Design Quality is desirable. What you need to know
The OpportunityTeam Horizon has a vacancy for Quality Assurance Specialist on site in a leading pharmaceutical company in the midlands. Acts as quality point person, providing guidance and feedback on quality assurance issues
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.
Excellent opportunity for a Quality/Reg Affairs officer to join a small, veterinary, medicines manufacturer. I have a fantastic opportunity for a Reg Affairs/Quality Officer with a background in pharmaceutical manufacturing and a minimum of a level 7 certification in Quality for Manufacturing or Regulatory affairs related to manufacturing.
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.
They will apply project management techniques in driving a structured approach to optimize process improvement for increased productivity, quality & reduce waste. Work with local facility stakeholders to develop/deliver annual programs to optimize process improvements for increased productivity, quality and reduced waste levels.
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