Global Regulatory Jobs in Limerick

Life Science Recruitment Ltd - Limerick

Pharmacopeia and/or European Pharmacopeia and ICH guidelines related to CMC regulatory topics. Provide oversight in the development of CMC strategies to support global regulatory strategy and submissions 70000.0

from: irishjobs.ie - 3 days ago

Cook Medical - Limerick

manner. Responsibility for assessing Regulatory Intelligence from a QMS perspective and ensuring compliance is maintained. Responsibility for implementing and maintaining Global Good Documentation 12000.0

from: irishjobs.ie - 3 days ago

Limerick, County Limerick, Ireland

team with activities that focus on implementing and optimizing quality engineering practices while ensuring a culture of quality and compliance with global regulatory requirements. Experience

from: jobleads.ie - More than 30 days ago

Regeneron Ireland DAC - Limerick

Contributing to global projects aimed at harmonizing laboratory data systems Reviewing updates to regulatory guidelines for electronic data systems to ensure ongoing compliance Coordinating the needs of QC 12000.0

from: irishjobs.ie (+1 source) - 5 days ago

Cook Medical - Limerick

. Reporting to: Team Lead, Regulatory Affairs or Manager, Regulatory Affairs Responsibilities Maintain an excellent understanding of global medical device regulations for specific jurisdictions as assigned 12000.0

from: irishjobs.ie - 16 days ago

Hollister Incorporated - F26 F3X5 Ballina, MY, IE

that there is a systematic application of policies, procedures, and practices. As a member of the Global Quality & Regulatory Affairs Senior Leadership team this role represents the Global Quality & Regulatory Affairs

from: Hollister Incorporated - 16 days ago

Cook Medical - Limerick

Overview The 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 12000.0

from: irishjobs.ie - 18 days ago

Vitalograph - Ennis, County Clare, IE

experience. Minimum of 3 years directly managing a team. In-depth knowledge and understanding of clinical trial process. Thorough knowledge of current regulatory and ICH GCP requirements and experience Competitive

from: bidrecruit.io - 19 days ago