Regulatory Affairs Associate Jobs in Ireland

Job Description SummaryThe Systems QA Specialist provides Quality System (QMS) support and oversight for a sterile manufacturing site operating terminal sterilisation within an aseptic filling environment. The role focuses on strengthening and maintaining compliant quality systems that enable safe e...

OverviewThe primary role of the Project Manager 1 is to provide support for the daily activities associated with global regulatory projects including communicating with the various teams on regulatory projects. Reporting to: Director Regulatory AffairsFind out more about Cook Medical hereResponsibil...

This is a handson regulatory role where your expertise directly supports product compliance patient safety and business continuity.As Regulatory Affairs Specialist you will partner closely with Quality R&D and Operations teams to apply regulatory requirements across our invitro diagnostic portfolio....

McDermott Laboratories LimitedViatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands combining the best of both to more holistically address healthcare needs globally. With a mission to empower people worldwide to live healthier at eve...

Hybrid schedule - Lake County - (Onsite Tuesday Wednesday Thursday)1 year to startManagers UpdateLooking for project managementWorking with a lot of teamsWorking with a regulatory agencyProject management of process improvementExperience with the regulatory system and Change managementPMP is preferr...

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...

JOB DESCRIPTION:About AbbottAbbott is a global healthcare leader creating breakthrough science to improve peoples health. Were always looking towards the future anticipating changes in medical science and technology.Our nutrition business develops science-based nutrition products for people of all...

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...

About Aerogen:Headquartered in the vibrant city of Galway Ireland with offices around the world Aerogen is proud to be the world leader in acute care aerosol drug delivery. Recognised through multiple MedTech awards and ten-time winner of the Zenith award for Respiratory Care Excellence in North Ame...

About Aerogen:Headquartered in the vibrant city of Galway Ireland with offices around the world Aerogen is proud to be the world leader in acute care aerosol drug delivery. Recognised through multiple MedTech awards and ten-time winner of the Zenith award for Respiratory Care Excellence in North Ame...

About Aerogen:Headquartered in the vibrant city of Galway Ireland with offices around the world Aerogen is proud to be the world leader in acute care aerosol drug delivery. Recognised through multiple MedTech awards and ten-time winner of the Zenith award for Respiratory Care Excellence in North Ame...

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...

The Associate Manager CMC Regulatory Submissions Compliance supports the management of Clinical Trial Application (CTA) pre-submission review processes within CMC Regulatory this role you will coordinate and review documentation planned for submission to global health authorities ensuring consiste...

The Associate Director CMC Regulatory Affairs provides leadership for an assigned product portfolio with a focus on ex-US this role you will be responsible for the development and execution of global regulatory strategies for combination products and medical devices mentor Regulatory Affairs staff...

OverviewThe Director of Post-Market Surveillance and Clinical Evaluation leads the global strategy governance and compliance of Post Market Surveillance and Clinical Evaluation activities ensuring accuracy regulatory alignment and continuous improvement across markets through standardized systems an...