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Provides support and direction to all departments in respect of specific quality system elements to ensure business, quality and compliance goals are met - A minimum of 3-5 years’ experience in a doc control, quality or compliance role within the biological and/or pharmaceutical industry.
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.
Multiple Quality Specialists required for Cork based Biologics client, 1+ Years' experience in Quality/Compliance within the Pharma or Medical Device industry - The Quality Specialist will participate and comply with the Quality Management System (QMS) requirements, including ownership.
Support start-up activities from a quality aspect to ensure compliance - Support all quality and compliance requirements for the Biologics Integrated Process Team (IPT) to enable batch disposition for each batch manufactured.
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.
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This site is expanding rapidly due to the inception of a new project and as such they require a Quality Specialist to join their Quality team. As the Quality Specialist you will be required to provide Quality oversight, along with supporting the teams within the site with GMP activities, Operational Quality and Quality Systems.
The Principal Quality Specialist will provide Quality oversight, support and expertise to GMP related activities and Quality Systems across the site and in meeting the Manufacturing Division (MMD) Priorities of: Compliance, Supply, Strategy and Profit Plan.
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 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.
The purpose of this role is to ensure compliance and regulatory requirements are met and to participate in developing Standard Operating Procedures to ensure quality objectives are met. Reviews routine manufacturing, environmental monitoring and quality control data for in-process and finished products.
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
Quality Officer They wish to recruit a Quality Officer to ensure that they are in compliance with regulatory requirements by timely review and release of batch documentation and conducting process, packing, cleaning and validation activities of all areas against the regulatory standards.
They are seeking a QA Specialist to join their team based in Cork. This is a superb opportunity to work in a Quality Assurance environment for a global pharma giant that serve patients with life-improving treatments.
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.
Our client, a Pharmaceutical company is currently recruiting a Quality Specialist for a 23-month contract in Cork. The Quality Assurance Associate reports to the QA CMO Manager, and is responsible for supporting operations and assisting with the batch release process for drug substance and drug product.
About the job: The Lead QA Specialist/Senior OP is responsible for managing and drive the site QA systems in conjunction with other Specialists in the QA Product Quality team. The are seeking a Lead QA Specialist to join their team on a permanent contract.
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.
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).
The QA Compliance Specialist maintains site compliance of operations inclusive of but not limited to Manufacturing, Quality Systems, QC, QA, Facilities Maintenance, Materials Handling, and QA Validation in accordance with mandated regulatory requirements and site expectations.