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Regulatory Affairs Jobs in Cork

1 - 15 of 35
1 - 15 of 35
Search Results - Regulatory Affairs Jobs in Cork
Beckman Coulter Diagnostics-Cork
Regulatory Affairs Specialist  •  12 month FTC  •  Maternity Cover Join to apply for the Regulatory Affairs Specialist  •  12 month FTC  •  Maternity Cover role at Beckman Coulter Diagnostics Regulatory Affairs Specialist - 12 month FTC -Maternity Cover...
Stryker Corporation-Cork
Regulatory Affairs Manager page is loaded Regulatory Affairs Manager Apply locations Cork, Ireland time type Full time posted on Posted Yesterday job requisition id R543519 Work Flexibility: Onsite Regulatory Affairs Manager- candidate can come...
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Stryker-Cork
Quality & Regulatory Affairs Co  •  Op Placement 2026  •  Cork Join to apply for the Quality & Regulatory Affairs Co-Op Placement 2026  •  Cork role at Stryker Quality & Regulatory Affairs Co-Op Placement 2026 - Cork 14 hours ago Be among the first 25...
Eli Lilly and Company-Cork
Innovate, Accelerate, and Deliver.  •  Model the innovation, leadership behaviors, and regulatory excellence attributes as described in Global Regulatory Affairs white papers.  •  Participate in forums that share regulatory information across GRA components...
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Eirgen Pharma-Cork
About the Job The Senior Regulatory Affairs Specialist is responsible for supporting regulatory activities associated with the registration of Eirgen/OPKO human and veterinary products across global markets, including the US, EU, and Japan. The role...
Eli Lilly and Company-Cork
in Global Regulatory Affairs white papers.Participate in forums that share regulatory information across GRA components and other Lilly teams and business partners.Collaborate effectively with business partners and stakeholders.Minimum Qualification...
Eli Lilly and Company-Cork
Regulatory Scientist leads, in partnership with the GRA-CMC Regulatory Scientist, the various aspects of global marketing authorization submission management processes. The Cork CMC Regulatory Scientist partners with GRA-CMC Regulatory Scientist to help...
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Stryker Ireland-Cork
This is a 12 month contract with full Stryker benefits. What you will do: Assesses regulatory intelligence to assist in the development of local, regional, and global regulatory strategies Participates in advocacy activities of a technical...
Stryker-Cork
Join to apply for the Regulatory Affairs Manager role at Stryker 1 week ago Be among the first 25 applicants Join to apply for the Regulatory Affairs Manager role at Stryker Get AI-powered advice on this job and more exclusive features...
Stryker Ireland-Cork
with international manufacturing sites to resolve issues. Posts finalised technical documentation and review checklists to a central repository. Reports compliance metrics to the Sr Regulatory Affairs Manager, CEOT and works with the EMEA RAQA team to plan...
Stryker Group-Cork
Key Areas of Responsibility:  •  Assess links between global, societal, and economic trends; stakeholder concerns; and regulatory issues; and determine implications for regulatory strategy.  •  Develop and update global, regional, and multi-country...
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Wallace Myers International-Cork
lifecycle, from concept to release  •  Collaborate with cross-functional teams including R&D, Quality, and Regulatory Affairs  •  Ensure software solutions are compliant with relevant medical device standards (e.g., IEC 62304, ISO 13485)  •  Contribute...
Eli Lilly and Company-Cork
Purpose: The purpose of the Regulatory Delivery and Excellence (RD&E) Global Submission Publisher role is to:  •  execute and maintain global regulatory submissions from candidate selection through end of product lifecycle.  •  provide maintenance support...
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Sanmina-Cork
is to ensure customer satisfaction by monitoring, controlling and improving all related customer processes. Principal customer interface for Quality metrics and improvement initiatives. Identifies, plans, and organizes regulatory affairs for ensuring compliance...
Stryker Ireland-Cork
a certificate in a related field (e.g. technical writer, engineer). You have many years of relevant professional experience in labeling, quality, regulatory affairs or R&D, ideally in the medical device, pharmaceutical or other regulated industries. You have...
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