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Search Results for Regulatory Affairs for Regulatory Affairs
Job Title. Location Salary Actions

Regulatory QC Specialist

Reg affairs / Compliance QC specialist Description My client manufactures and distributes X-ray and MRI Contrast Media for internal and external customers worldwide. As part of the Pharmaceutical Diagnostics (PDx) business, they support the PDx vision of being the best-in-class supply chain delivering the right dose to the right patient at the right time. At their campus at Co. Cork, they employ approximately 600 staff and are a 24/7 operation exporting to 93 markets worldwide. This is an opportunity for a skilled QC Specialist to join a team that manufactures and distrib...

Location: Cork, Cork City,
Regulatory QC Specialist
Cork Not Disclosed

Scientific Officer - Cyber Intelligence

ROLE SUMMARY The Scientific Officer (Cyber Intelligence) role is based within the Enforcement Section of the Compliance Department, reporting to an experienced Enforcement Intelligence Officer. Responsibilities of the Scientific Officer (Cyber Intelligence) are broad ranging and focused on supporting the Enforcement Section to garner actionable intelligence from cyber sources which will be utilised to assist an intelligence led Enforcement process. The Scientific Officer (Cyber Intelligence) will work to support my client to enhance its analytical capabilities in order to ...

Location: Dublin, Dublin City Centre,
Scientific Officer - Cyber Intelligence
Dublin Not Disclosed

Director, Clinical Development (Oncology)

Our client is a global Biopharma who have recently established a Clinical Trials Centre of Excellence in Dublin, Ireland. They are seeking a clinical development professional with extensive drug development (early phase I) experience, preferably with Oncology Clinical trial experience, in the area of Haematology or related therapeutic area. They are open on therapeutic area the person come from. The successful person shall lead multiple components of clinical trial programs in paediatric oncology clinical development. For the assigned projects, you will be accountable ...

Location: Dublin,
Director, Clinical Development (Oncology)
Dublin Not Disclosed

Assoc MDR/Vigilance Specialist

We’re currently recruiting for an exciting opportunity with an award-winning medical device organization based in Galway. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. You will be part of a high performing Complaint Handling and Medical Device Regulatory reporting department, which provides value throughout the Product Life cycle through world class execution in Medical Device Reporting and Vigilance compliance. Responsibilities Responsible for the co-ordination of complaint ha...

Location: Galway,
Assoc MDR/Vigilance Specialist
Galway Not Disclosed

Clinical Regulatory Associate

Clinical Regulatory Associate Our client, a global pharma company are currently recruiting for a Clinical Regulatory Associate to join their team on a permanent basis. As Clinical Regulatory Associate you will beaccountable for the operational and technical registration management processes that support the expedited delivery of safe and effective products to patients. Responsibilities Lead the registration management process by providing expertise in electronic submission regulations and guidance and technical content for which includes INDs, NDA, BLAs, NDSs, and oth...

Location: Cork,
Clinical Regulatory Associate
Cork Not Disclosed

Snr Associate QA

We’re currently recruiting for an exciting opportunity with an award-winning pharmaceutical organization based in Dublin This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Duties 24/7, 12hr shift role - Eye Test Required for this position - Inspection Role. Primarily dealing with manufacturing activities, troubleshooting issues in production. Quality contact on deviations. Batch record review for manufacturing. SOPs. filling, setups and work on lines, inspection, triage issues relati...

Location: Dublin,
Snr Associate QA
Dublin Not Disclosed

Clinical Publisher Associate

Clinical Publisher Associate Our client, a global pharma company are currently recruiting for a Clinical Publisher Associate to join their team on a permanent basis. As Clinical Publisher you will create and maintain complex strategic and compliance submissions through collaboration, document management, and internal database maintenance. You will collaborate with Regulatory Associates, Regulatory Scientists, cross-functional contributing/authoring areas, and affiliates to align on submission specific strategies and to ensure adherence to eCTD regulations and guide...

Location: Cork,
Clinical Publisher Associate
Cork Not Disclosed

MDR/Vigilance Specialist

We’re currently recruiting for an exciting opportunity with an award-winning Medical Device organization based in Galway. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Duties Responsibilities may include the following and other duties may be assigned. Monitors the company's drug or medical devices surveillance program including the intake, protocol development, evaluation, processing, and follow up on adverse reports, participation in the resolution of any legal liability and in...

Location: Galway,
MDR/Vigilance Specialist
Galway Not Disclosed

Senior EHS Specialist

We’re currently recruiting for an exciting opportunity with an award-winning pharmaceutical organization based in Cork. This is an excellent position for

Location: Cork,
Senior EHS Specialist
Cork Not Disclosed
Other Regulatory Affairs Jobs
Job Title Location Salary Actions
Clinical Publisher Associate Cork Not Disclosed
Clinical Regulatory Associate Cork Not Disclosed
Clinical Regulatory Associate Cork Not Disclosed
Clinical Publisher Associate Cork Not Disclosed