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Experienced Medical Device Quality specialist required for a blue chip international medical devices company. QA Specialist For further information on this or other Quality roles within Medical Devices and Pharma in Ireland please contact Hazel Whelan in Recruitment Plus or email CVs in confidence. 11 month contract - Dublin
Our Waterford based client are currently recruiting for a Quality Specialist to join their team on a permanent basis. They are currently seeking a Quality Specialist based to join their team based in Waterford on a permanent basis. • Support the overall Quality Program (ISO 9001, 2015).
The Global Quality External Manufacturing organisation is seeking to recruit a Quality Operations Senior Specialist for its operation based in Dublin. The position will be responsible for supporting the coordination of quality events, change control and market complaints programs in respect of Third Party Manufacturer relationships.
A leading Pharma site requires an Automation Specialist to provide support to the Quality Department. Working within the Quality Support function, this role will provide Quality leadership, coordination, oversight and direction to the development, implementation and execution of process validation and technical transfer project activity.
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Due to rapid expansion, our client seeks an experienced Supplier Quality Specialist who will act an Incoming Quality representative with vendors on all incoming materials. Ideal candidate will identify and drive quality improvements through project management initiatives.
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.
A thriving bulk pharmaceutical company based in Cork are looking for a Quality Validation Specialist to join their team. If so, you could be the Quality Validation Specialist that we have been looking for. Role: Quality Validation Specialist Your role as the quality validation specialist will be in a new project the company are starting.
You be primary responsible for regulatory affairs, quality systems, compliance with cGMP’s, in addition support release of finished product and investigation of product issues.
The QUALITY & REGULATORY SPECIALIST will be responsible for regulatory affairs, quality systems, compliance with cGMP's, in addition support release of finished product and investigation of product issues.
QA Specialist- External Supply Operations, Novartis, Ringaskiddy, Ireland Quality Assurance Specialist The purpose of the role is to provide GMP support for the External Supply Operations (Chemicals) quality control and QA related activities performed for the materials under the scope of ESO (Chemicals) responsibility, particularly API materials.
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.
The QA Specialist is expected to adhere to all cGMP compliance and regulatory mandates and quality requirements, and comply with all SOPs and internal organisation policies and procedures in the performance of job duties.
The site at Newbridge is a solid dose / packaging site and the Quality Specialist roles support a variety of aspects of the site operations including Quality Systems, Operations Support & Projects. We have an exciting opportunity for a number of QA Specialists to join the team. We have approximately 30 colleagues on our Quality Assurance team.
Our Client a well established Logistics Provider now require a Quality & Compliance Officer, To coordinate Safety and Quality issues for all sites in a timely, efficient and accurate manner.
Maintain accreditation and liaise with departments on site quality issues. The QMS officer will be responsible for up keeping and maintaining the Site QMS system to FSSC standards , HACCP site team lead , communicate and maintain the audit schedule for the site - Maintain QMS to meet customer and regulatory requirments
Abbott Diagnostics Division Longford are seeking a Quality Professional Quality System Compliance: Maintains awareness of standards that regulate our industry. Maintains vigilance to ensure adherence to Quality Policy and Quality system procedures by promptly reporting noncompliance issues to management.
The successful applicant must be able to work effectively with a team or those outside the formal line of authority to accomplish organisational goals The OpportunityTeam Horizon is looking to speak with a Quality Assurance Specialist regarding a contract position.
The Quality Assurance Officer is expected to conduct client to CAREGiver introductions and perform quality assurance visits in order to provide the highest quality service to clients. The Quality Assurance Officer is expected to perform a variety of duties in the area of client services.
Site QA Specialist required for client site in Athlone - Acts as quality point person, providing guidance and feedback on quality assurance issues. Deliver Quality Assurance review and approval of SOPs, master batch records, policies, operational standards, validation protocols and reports as required.
The Quality officer will be responsible for working with the Quality department on the management associated with the quality management system including the management of all templates; managing all changes to the companies intranet; managing the corrective action process and expediting closure of ...
This individual will support the QP functions at Shire Pharmaceuticals Ireland Limited by assuring compliance of medicinal products through a review of associated batch documentation and quality system components. This individual will work in the EU Quality Operations sub-group of Shire Pharmaceuticals Ireland Limited, Dublin, Ireland.
The Quality Assurance Officer will be responsible for supporting Quality Systems and ensuring GMP compliance across the site. Role: Quality Assurance Officer * Preparation of Annual Product Quality Review reports. * Experience of working in a similar Quality Assurance related role in the Pharmaceutical Industry.