Regulatory Affairs Jobs in Ireland

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

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 Senior Manager CMC Regulatory Submission Compliance is responsible for aligning the regulatory landscape with country-specific requirements and supporting clinical regulatory submission activities supply planning and QP certification. This role leads processes and cross-functional coordination e...

As QC Operations Team Lead (FTC 12 months) you will be responsible for ill be responsible for carrying out tasks and projects relating to QC instruments/equipment computer systems sample management and general QC-compliance functions while ensuring the highest standards of Good Laboratory Practices...

As QC BioAssay/Biochemical Assay Lead (Associate Director) you will play a pivotal role in ensuring the highest standards of professional excellence regulatory adherence and quality within the business with overall responsibility for the management of product testing teams including bioassays and bi...

As QC Microbiology Lead (Associate Director) you will play a pivotal role in ensuring the highest standards of professional excellence regulatory adherence and quality within the business with overall responsibility for the management of product testing and Environmental Monitoring teams. Working cl...

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...

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...

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 the roleThe purpose of this role is to perform quality control inspections on the production floor to ensure products production processes and documentation meet required procedures. The successful candidate serves as the first-line point of contact for in-line Quality queries accurately docum...

The RoleWe are seeking a highly capable Senior Compliance Specialist Enterprise Compliance Advisory to partner with Vanguard Europes key enterprise functions (Operations IT Cyber Security Finance) to provide proactive commercially minded compliance advice guidance and oversight. This role plays a c...

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...

Work Flexibility: Hybrid or Onsite12 month contract with full Stryker benefits.What you will do:As a member of the Technical Publications team create and revise product labels to meet labeling requirements for medical devices. Collaborates with product subject matter experts to gather and assess lab...

About PSC Biotech Who are we PSC Biotech is a leading Biotech Consultancy firm founded in 1996 headquartered in Pomona California USA with Global operations in Ireland India Singapore Australia and the US serving 350 clients in more than 23 countries worldwide. We provide cloud-based software soluti...

About the roleThe Research Scientist manages the core research and future innovation service and new product innovation pipeline for Avery Dennison Medical Longford. This role involves liaising with Advanced Research & Development (ARD) and Corporate partners on strategy and innovation while collabo...