Regulatory Submissions Jobs in Cork

Join our team of experts in regulatory and ethics submissions of clinical studies. You will focus on facilitating the start of research projects of novel medicinal products in Kazakhstan while taking a step further in your professional career.Office-based in AlmatyYou will:Prepare clinical trial sub...

Work Flexibility: Hybrid or OnsitePosition summaryPartner with Engineering and Advanced Operations to define design requirements and develop manufacturing processes to support new product development projects. Lead risk management activities to ensure the highest level of product and process quality...

Work Flexibility: Hybrid or Onsite(23 month fixed term contract)Key Areas of Responsibility: Assesses regulatory intelligence to assist in the development of local regional and global regulatory strategiesEvaluates the regulatory environment and contributes to providing internal advice throughout th...

Role can be based from Athlone Cork or Dublin site. Introduction to role:In Alexion Technical Operations (ATO) we work closely with Alexions manufacturing network of internal sites and external manufacturing partners our colleagues in Development Quality Regulatory Supply Chain and Commercial Operat...

Job DescriptionOverviewAtkinsRéalis is seeking an experienced and motivated Senior Architect to join our expanding architectural team in Ireland. With a strong and diverse pipeline of medium to large-scale projects across aviation industrial education transportation mixed-use and civic sectors this...

Work Flexibility: Hybrid or Onsite12 month Hybrid contract in our Innovation Centre CorkWhat you will do:: Assesses regulatory intelligence to assist in the development of local regional and global regulatory strategiesEvaluates the regulatory environment and contributes to providing internal advice...

Work Flexibility: Hybrid or OnsiteThis is a Hybrid 23 month contract with full Stryker benefitsWhat you will do:Develop quality assurance documentation to support product transfer activities and regulatory submissions.Support quality system maintenance for the design control process by identifying a...

Work Flexibility: Hybrid or Onsite****12 months fixed term contract (Hybrid role)****Key Areas of Responsibility Provides regulatory affairs support to the Patient Specific Solutions business to achieve timely approvals of custom devices via custom and compassionate use pathways.Assesses regulatory...

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High PerformanceAt Boston Scientific well give you the opportunity to harness all thats within you by working in teams of diverse and high-performing employees tackling some of the most important health industry challenges. Wi...