Regulatory Affairs Specialist IVD Jobs in Ireland

At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. Youll lead with purpose breaking down barriers to innovation in a more connected compassionate world.A Day in the LifeMedtronicAt Medtronic we value what makes you...

Career CategoryRegulatoryJob DescriptionThe Regulatory Affairs Manager at Amgen ensures the companys compliance with all regulations and laws pertaining to the companys business. They work with federal state and local regulatory agencies on issues and regulations that affect the companys products an...

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...

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...

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....

Scope of Role:The role is based in Sydney and may require some local and interstate travel. The role encompasses a range of pre and post market product activities and requires:interaction and negotiation with regulatory agencies in Australia and New Zealand;collaboration across local regional and cr...

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...

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...

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...