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Search Results for Biopharmaceutical
| Job Title. | Location | Salary | Actions |
Medical AdvisorMedical Advisor Our client is a leading Biopharmaceutical organisation, based in Dublin. They are seeking a Medical Advisor to join an established team for a duration of 12 month contract. The Medical Advisor shall report to the Head of Medical Affairs. Role/Responsibilities: • Provide scientific support to internal and external customers in response to clinical interest. • Deliver the sharing of knowledge to internal stakeholders e.g. through provision of training to help to ensure highest standards of brand/therapy expertise in customer facing teams ...Location: Dublin, |
Dublin | Not Disclosed | |
R&D Formulation Scientist (Healthcare)Our client is an Innovative organisation, based in Dublin. They are seeking an expert in Formulations of gels, ointments, eye drops & creams to join an established & growing team. Reporting to the NPD Director, the R&D Formulation Chemist will explore and develop innovative meaningful formulations and lasting solutions that patients can understand and identify with. The successful candidate will bring new projects to life from early evaluation, formulation development and work with internal and external stakeholders to ensure a well-executed and successful ...Location: Dublin, |
Dublin | Not Disclosed | |
Senior QC LIMS EMPOWER SpecialistWe’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Dublin This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Duties We are looking for candidate that have Administrator or Superuser experience LIMs and/or Empower QC lab experience would be useful Min Requirements: - Experience (5 years) in a similar role (Quality Systems, computer related systems, and biotechnology in a regulated biotechnology, pharma...Location: Dublin, |
Dublin | Not Disclosed | |
Director (Clinical Trial Disclosures & Data Transparency)Our client is a leading global Biopharmaceutical organisation, based in Dublin. The Disclosures & Transparency function resides organisationally within the Regulatory Documentation and Submissions division and is responsible for Clinical Trial Disclosure and Data Transparency activities. These activities include the registration of, and results posting of sponsored clinical trials on appropriate Clinical Trial Registries, the generation and facilitation of clinical trial/clinical product transparency activities and deliverables in accordance with relevant laws, regulations...Location: Dublin, |
Dublin | Not Disclosed | |
Associate Manager (Technical Training)Our client is a Global Biopharma based in Limerick. They are currently seeking an Associate Manager for their Technical Training who will focus on Instructional Design. This organistaion seeks people who are excited by a start-up environment, recognize the opportunities that this offers and want to be challenged. The successful person shall be responsible for leading instructional design within Technical Training, managing the eLearning program, training delivery standards, incorporating emerging learning techniques and technologies into the global training program. Role...Location: Limerick, |
Limerick | Not Disclosed | |
CMC Regulatory Affairs Senior ManagerCMC Regulatory Affairs Senior Manager Our client, a global pharmaceutical organisation based in Cork are currently recruiting for a CMC Regulatory Affairs Senior Manager to join their global regulatory affairs group on a permanent basis. As CMC Regulatory Affairs Senior Manager you will manage the CMC submission management processes by leveraging expertise to optimize internal processes and tools. Responsibilities Manage the CMC submission management processes by leveraging expertise to optimize internal processes and tools processes and tools. Anticipate and resolve pr...Location: Cork, |
Cork | Not Disclosed | |
Regulatory Affairs Manager (EMEA)A Regulatory Affairs Manager (EMEA) is required to join a leadingMedical Device organisationin Athlone . Your role: As the Regulatory Affairs Manager you will be responsible for determining and supporting the regulatory activities which lead to, and maintain regulatory compliance and approval for company products globally. Your responsibilities: Primary responsibility for regulatory affairs in the EMEA region. Pursue relevant information pertaining to new developments in regulatory affairs by maintaining contact w...Location: Roscommon, |
Roscommon | Not Disclosed | |
NPD Project Manager (Healthcare)NPD Project Manager Our client is a leading Healthcare company, based in Dublin. Reporting to the New Product Development (NPD) Director, the NPD Projects Manager will give full support to the delivery of NPD projects. The New Product Development Projects Manager supports and interacts within a team dedicated to developing and creating meaningful and lasting solutions that patients can understand and identify with. As an important member of the NPD team, the Product Development Projects Manager is responsible for assisting in the work-flow for the development of multiple proje...Location: Dublin, |
Dublin | Not Disclosed | |
Clean Utilities EngineerThe Clean Utilities Engineer will perform an integral role in the development of the company. You will take ownership for the clean utilities (such as, but not limited to, Water for injection, clean steam, clean dry air, nitrogen) and the clean utilities equipment. You will provide leadership, cross functional support and technical expertise to IUFT, maintenance and manage their operation through design, construction, validation, start-up and commercial manufacturing. Ensure that objectives are effectively achieved, consistent with the company’s requ...Location: Carlow, |
Carlow | Not Disclosed | |
Scientific Communications Publication Capability LeadOur client, a global pharmaceutical organisation are currently recruiting for a Scientific Communications Publication Technical Advisor to join their team. As Publication Capability Lead you will help drive launch and publication capabilities and operational excellence for the Global Scientific Communications Group. Responsibilities Function as an expert on the publication medical writing, publication processes and practices, including authorship, transparency and ethics Consults and advise site publication writers on issue management and escalation Represent the gro...Location: Cork, |
Cork | Not Disclosed | |
Regulatory Scientific Communications AssociateOur client, a global pharmaceutical organisation are currently recruiting for a Scientific Communications Associate to join their newly created Global Scientific Communications team. As Regulatory Scientific Communications Associate you will work with cross-functional, multidisciplinary teams to lead the development of documents intended for regulatory audiences including, clinical study reports, briefing documents, regulatory responses, Investigational New Drug Applications, and marketing authorization applications. Responsibilities Document Preparatio...Location: Cork, |
Cork | Not Disclosed | |
Sr Associate QCWe’re currently recruiting for an exciting opportunity with an award-winning pharmaceutical organization based in Dublin. This is an excellent position fLocation: Dublin, |
Dublin | Not Disclosed | |
Sr Associate QCWe’re currently recruiting for an exciting opportunity with an award-winning pharmaceutical organization based in Dublin. This is an excellent position fLocation: Dublin, |
Dublin | Not Disclosed | |
QA SpecialistWe’re currently recruiting for an exciting opportunity with an award winning pharmaceutical organization based in Cork. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Duties •This position is responsible for carrying out tasks and projects related to management of Quality Assurance activities as required by Good Manufacturing Practice (GMP). These activities include Incoming material release, Batch release, Change control, Event management, Supplier qualification%...Location: Cork, |
Cork | Not Disclosed | |
Scientist Data AnalyticsWe’re currently recruiting for an exciting opportunity with an award winning pharmaceutical organization based in Cork. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Duties • The Data Analyst will contribute to development of Automated reports and Visualizations. Specifically, the Scientist will create statistical models and visualizations that integrate many types of data to create comprehensive models. Models will then be applied to determine stability of Product and ...Location: Cork, |
Cork | Not Disclosed | |
Sr Associate QC (Senior)We’re currently recruiting for an exciting opportunity with an award-winning pharmaceutical organization based in Dublin. This is an excellent positionLocation: Dublin, |
Dublin | Not Disclosed | |
QA SpecialistWe’re currently recruiting for an exciting opportunity with an award winning Biopharmaceutical organization based in Cork. This is an excellent opportunitLocation: Cork, |
Cork | Not Disclosed | |
QA SpecialistWe’re currently recruiting for an exciting opportunity with an award winning Biopharmaceutical organization based in Cork. This is an excellent opportunitLocation: Cork, |
Cork | Not Disclosed | |
QA SpecialistWe’re currently recruiting for an exciting opportunity with an award winning Biopharmaceutical organization based in Cork. This is an excellent opportunitLocation: Cork, |
Cork | Not Disclosed |
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Regulatory Affairs | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: info@regulatoryaffairs.ie
Copyright © 2012 Life Science Recruitment Ltd
This site uses cookies. For more information on our cookie policy read our Privacy Policy | Terms of Use
Registered as a private limited company. No: 445328 | Web Design / SEO by WebScience | Valid XHTML - CSS