Please enter your email address
Please enter a valid email address
This position reports to the Quality Lead CoE and will be part of the Quality Organisation at Carlow. Review of site documentation for regulatory impact (for example – Product Spec Files, QC documents, EBR updates, Quality Notifications, Stability protocols and reports, Validation protocols and reports, process description).
12 Month contract for a Quality Officer in a leading pharmaceutical company based in Waterford City. New Product/Validation: Quality support for introduction of new products, equipment and facilities.
The role is required to manage the incoming quality department and is required to assist us in the ramp up of commercial voluemes on site. This lab manager will lead a team of analysts, specialists and technicians and hence will be responsible for people aspects, such as coaching, talent development, recruitment and performance management.
Senior Regulatory Affairs Specialist is required for leading Leinster based pharmaceutical multinational, providing regulatory support for clinical and commercial pharmaceutical products - Senior Regulatory Specialist Career advancing opportunity within a global pharmaceutical leader based in the Leinster region.
Working with the LotusWorks group as a Quality Technician, you will ensure all samples received are sampled and tested to the highest standards of GMP and safety to meet customer targets. Laboratory Quality Systems - About Us - A valued and trusted partner to the world’s leading companies.
Please enter your email address
Please enter a valid email address
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.
A leading Food manufacturing company based in the Kilkenny / Carlow region, has an opportunity for an experienced Quality Assurance Manager for a 12 month maternity contract. · 2+ years experience at a Quality Manager Level. · Management of Site Quality Management system to BRC Standard
Quality Assurance Specialist - Pharmaceuticals- Tipperary - The ideal candidate will have strong Quality and Technical understanding of Operations and Compliance requirements in the Pharmaceutical Industry. Supports the site compliance plan and quality metrics generation - Provide Quality support to Deviation and Laboratory OOS investigation.
New Permanent Quality Specialist role available with Global Pharmaceutical Group in Dublin - See below for details. This company develops, manufactures, markets and distributes quality branded and generic pharmaceutical products as well as over-the-counter medications through its operating companies.
The role of Quality Assurance Specialist will be to establish the quality management system and encourage a quality culture from within the Quality Team. POSITION TITLE: Quality Assurance Specialist REPORTING TO: Quality Manager - To establish, organize and maintain a Quality Management System for a new DS manufacturing facility
The Quality Services Content Specialist is responsible for a specialised area of content and information within the Operations division - The Quality Services Content Specialist looks after procedures, webpage articles, templates and other type of content, all while ensuring that the Group’s content strategy is properly implemented.
The Quality Specialist Dublin is responsible for supporting the manufacture of product at DCC Vital Contract Manufacturing Organisation (CMO) sites, under the management of Quality Operations. Foster and promote GMP, GDP and the associated Quality Management Systems within the site
Working within the Technical Team as a Quality Officer you will work alongside the Quality Manager maintain and refine the companies QA System. Drive quality in Low Risk and high risk in terms of food safety and Product Quality resulting in improved audit results and reduction in customer complaints
The successful candidate will play a key role in the management of site Quality Systems to ensure that high quality product is delivered on time to customers. Quality batch documentation review and control - Support quality audits where necessary - Provide Quality input to process/product investigations (including planned / unplanned deviations)
Incoming QA Specialist required for leading Dublin based biopharmaceutical multinational. Provide quality support and investigation of all classes of non-conformance events - Must be degree qualified with 4+ years previous experience. We are actively seeking to recruit a QA Senior Associate for our client site, a Dublin based pharmaceutical multinational.
An opportunity has arisen for a Senior QA Specialist within a Dublin based pharmaceutical multinational. An opening for a Senior QA Specialist has arisen within a leading Dublin based pharmaceutical multinational.
BMS Cruiserath Biologics is seeking to recruit a temporary Senior QA Compliance Specialist - Supplier Quality Management. BMS Cruiserath Biologics is seeking to recruit a temporary Senior QA Compliance Specialist - Supplier Quality Management to join the Quality Systems and Compliance team to provide maternity leave cover for 9-12 month duration.
BMS Cruiserath Biologics is seeking to recruit a permanent QA Specialist specializing in QA Operations. Reporting to the QA Operations Manager, the QA Specialist will provide QA oversight and support construction, qualification and validation, technical transfers, regulatory approvals and commercial operations.
Principal Responsibilities of Quality Assurance Specialist - Distribution - Assess cold chain shipments and provides corresponding quality decision on product. Provide guidance, drive and monitor Quality issues related to cold chain and GDP to resolution within the company and with external parties.
BMS Cruiserath Biologics is seeking to recruit a permanent QA Compliance Specialist to join the Quality Systems and Compliance team. Reporting to the QA Compliance Manager, the QA Compliance Specialist will provide QA oversight and support qualification and validation, technical transfers, regulatory approvals and commercial operations.
As part of the Quality team, the QA Specialist is responsible for the validation and monitoring of microbiological/ particle testing processes that is required to support plant operations. Must have a third level qualification in Engineering/Quality/Science.
Quality Officer (EMEA) required for large Global Pharmaceutical Company. To ensure that EMEA Quality Release targets are achieved by ensuring that all batch documentation & supporting documents from in-network and 3rd party suppliers are received in an accurate and timely manner. To update & maintain the daily Quality Management List.
The Quality Assurance Officer is responsible for supporting Quality Systems and ensuring GMP compliance across the site. • Preparation of Annual Product Quality Review reports. • Generation and reporting of Quality metrics monthly. • Other duties as required and as directed by the Quality Assurance Manager.
In conjunction with the CPL Group they are looking to set up a new startup manufacturing facility and are looking to recruit for a Quality Specialist for its new facility based in Athlone.
QA Specialist required for a multinational pharmaceutical company based in Cork and also in Dublin QA Specialist This position is responsible for carrying out tasks and projects related to management of Quality Assurance activities on site as required by Good Manufacturing Practice (GMP).