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Search Results for Scientific
Job Title. | Location | Salary | Actions |
Senior Director, Regulatory Affairs (Biopharma)Our client is a research-based biopharmaceutical company. They deliver life-saving therapies to patients in need. With the commitment and drive you bring to theLocation: Dublin, |
Dublin | Not Disclosed | |
Regulatory Project ManagerRegulatory Project Manager Our client, a growing biotech organisation are currently recruiting for a Regulatory Project Manager to join their organisation on a permanent basis. As Regulatory Project Manager you will be responsible for the coordination and the day-to-day support of the regulatory affairs strategy and operational activities of the organisation. As Regulatory Project Manager you will provide support to both CMC, non-clinical, and clinical development. Responsibilities Coordinate input from external regulatory affairs consultants, identify and close knowledg...Location: Dublin, |
Dublin | Not Disclosed | |
Senior Project ManagerWe’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 •Arrange agreement among the project team, customers, and management on the goals of the project • Develops and maintains the Project schedule/plan that addresses quality, objective, scope, cost, schedule, resources and responsibilities - to deliver the project, and measure...Location: Dublin, |
Dublin | Not Disclosed | |
Senior Quality Assurance 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 •The Quality Assurance (QA) Specialist is a senior and active role within the broader QA function. •The QA Specialist will typically report to a QA Senior Manager and will be required to be a Subject Matter Expert in their assigned area of responsibility. •QA specialists will b...Location: Dublin, |
Dublin | Not Disclosed | |
Clinical Regulatory AssociateClinical Regulatory Associate Our client, a global pharma company are currently recruiting for a Clinical Regulatory Associate to join their team on a permaneLocation: Cork, |
Cork | Not Disclosed | |
Regulatory Associate CMC (LO A008365)The Global Regulatory Affairs group islooking for an associate to lead and partner with Chemistry, Manufacturing and Controls (CMC) Regulatory Scientists in the various aspects of global marketing authorization submission management processes. This exciting opportunity will enable you to utilize your project management and communication skills to advance the submission process for new molecules. You will also partner with CMC Scientists to help build and manage submission content, provide guidance on structure and content placement within Common Technic...Location: Cork, |
Cork | Not Disclosed | |
Clinical Publisher AssociateClinical Publisher Associate Our client, a global pharma company are currently recruiting for a Clinical Publisher Associate to join their team on a permanent basis. As Clinical Publisher you will create and maintain complex strategic and compliance submissions through collaboration, document management, and internal database maintenance. You will collaborate with Regulatory Associates, Regulatory Scientists, cross-functional contributing/authoring areas, and affiliates to align on submission specific strategies and to ensure adherence to eCTD regulations and guide...Location: Cork, |
Cork | Not Disclosed | |
Director, Regulatory Affairs (Pediatrics/Infectious Diseases)Our client is a global Biopharma who are establishing a new Peadiatric Centre of Excellence in Dublin, Ireland. This is an exciting opportunity to lead a Pediatrics Regulatory Affairs function in the area of Infectious Diseases where you will provide global regulatory strategic and technical leadership of regulatory activities for pediatric product development. Role/Responsibilities: Responsible for providing strategic regulatory guidance on the development of global pediatric submissions, including those required in the US and EU. Responsible for leading all pediatric-...Location: Dublin, |
Dublin | Not Disclosed | |
Director of Clinical Pharmacology (Infectious Diseases)Our client is a leading Bio-Pharma who are establishing a new office in Dublin in the area of Clinical Research, with specific focus on Pediatric Trials. As a Director within the Clinical Pharmacology Group, the successful person will have ultimate responsibility and accountability for clinical pharmacology programs in the area of HIV and emerging viral infections. As a member of the Clinical Pharmacology team this person shall have unparalleled opportunity to be involved with every aspect of the product development process, from first-in human through approval, including ...Location: Dublin, |
Dublin | Not Disclosed | |
Quality and Regulatory Affairs ManagerQuality & Regulatory Affairs Manager Our client, a leading healthcare organisation are currently recruiting for a Quality and Regulatory Affairs Manager to join their team on a permanent basis. As Quality & Regulatory Affairs Manager you will be responsible for leading the regulatory affairs and quality assurance functions within the organisation. You will manage the department effectively to ensure compliance, continuous improvement and to ensure product quality and customer satisfaction. Responsibilities Provide Quality & Regulatory ...Location: Dublin, |
Dublin | Not Disclosed | |
Senior Tech Transfer LeadWe’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 This role will require the candidate to provide process development support primarily to new product introductions (NPI) and lifecycle management (LCM) changes. The candidate will establish themselves in a product lead role where the majority of input provided will be leading of process performance qual...Location: Dublin, |
Dublin | Not Disclosed | |
Senior R&D EngineerWe’re currently recruiting for an exciting opportunity with an award-winning Medical Device organization based in Galway. 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 Seeking an experienced engineer to focus on all stages of the product development process from concept generation through to commercializing of cutting-edge structural heart devices. This is an exciting opportunity to get involved in the rapidly growing world of Structural Heart. The role includes the fol...Location: Galway, |
Galway | Not Disclosed | |
Senior Manufacturing EngineerWe’re currently recruiting for an exciting opportunity with an award-winning Medical Device organization based in Galway. 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 At our Manufacturing Engineering Department, we focus on providing Stable, Flexible and Cost Effective Manufacturing processes that produce the highest quality products through innovative engineering services and solutions. Manufacturing Engineers are directly involved in maintaining and continuously ...Location: Galway, |
Galway | 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 |
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Regulatory Affairs | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: [email protected]
Copyright © 2012 Life Science Recruitment Ltd
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Regulatory Affairs | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: [email protected]
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







