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

Senior Associate Scientist (Technical Services)

Our client is a leading Biopharma, based in Cork. They are seeking an Associate Scientist for their technical Services team. The ideal person shall have a strong GMP background with 5+ years experience. Role/Responsibilities: Leads technical support activities related to maintaining commercial product supplies through management of internal and external resources. Contributes to and leads complex processes across functions and interacts effectively with the other team members to ensure product meets regulatory, performance, and cost requirements. Contributes to and...

Location: Cork,
Senior Associate Scientist (Technical Services)
Cork Not Disclosed

GMP Inspector

GMP Inspector Reporting to a GMP Inspection Manager, the GMP Inspector will be responsible for assessing the compliance of manufacturers with EU Good Manufacturing Practice (GMP). The Manufacturing Compliance Specialist will evaluate the compliance of sites inspected, in Ireland and abroad, with the requirements of National legislation European Community Directives, Regulations and Guidance. These sites may include; • Manufacturers and distributors of medicinal products. • Manufacturers of investigational medicinal products. • Sites involved in ...

Location: Dublin,
GMP Inspector
Dublin Not Disclosed

Director, PVE (Risk Management)

Our client is a global Bio-Pharma with a strong pipeline of products across a range of therapeutic areas from Infectious diseases, Inflammation & Oncology. They are seeking a Director of Pharmacovigilance & Epidemiology (Risk Management) to join a new team in Dublin. This team shall be a Centre of Excellence for global Paediatric clinical trials. The ideal person shall have a healthcare degree with a strong drug safety background. Role/Responsibilities: Signal detection and authorship of signal work-up documents in collaboration with a Medica...

Location: Dublin,
Director, PVE (Risk Management)
Dublin Not Disclosed

Associate Director, Pharmacovigilance & Epidemiology (PVE)

Associate Director, Pharmacovigilance & Epidemiology (PVE) Our client is a Global Biopharma who are establishing a new Centre of Excellence for Clinical Trials in Dublin. They are seeking an Associate Director who will manage Vendor Oversight Operations within PVE. Role/Responsibilities: Oversight of vendor(s) responsible for ICSR processing. This includes, but is not limited to: Scheduled and ad hoc meetings with the vendor(s) Oversight of training and quality metrics Review feedback and performance metrics relating to the vendor(s)f...

Location: Dublin,
Associate Director, Pharmacovigilance & Epidemiology (PVE)
Dublin Not Disclosed

Director of Clinical Pharmacology (Infectious Diseases)

Our client is a leading Bio-Pharma who are establishing a new office in Dublin in the area of Clinical Research. As a Director within the Clinical Pharmacology Group, the successful person will have ultimate responsibility and accountability for clinical pharmacology programs in the area of HIV and emerging viral infections. As a member of the Clinical Pharmacology team this person shall have unparalleled opportunity to be involved with every aspect of the product development process, from first-in human through approval, including post-marketing activities. In this role, ...

Location: Dublin,
Director of Clinical Pharmacology (Infectious Diseases)
Dublin Not Disclosed

Director, Quality & Compliance (GCP)

Our client is a global Biopharma organisation who play a crucial role in developing life-saving therapies. They are seeking a Clinical Quality and Compliance Director who is ready to dive-in to support our clients clinical development programs. As a Clinical Quality and Compliance Director, you will support and work with our clinical study management teams and teammates across R&D Quality and Compliance. They need someone with strong leadership skills, expert Good Clinical Practice (GCP) knowledge, audit skills, communication, facilitation skills, and the ability to...

Location: Dublin,
Director, Quality & Compliance (GCP)
Dublin Not Disclosed

Director, Pharmacovigilance Quality & Compliance (GVP)

Our client is a leading Global Biopharmaceutical organisation who play a crucial role in developing life-saving therapies. They are seeking a Pharmacovigilance Compliance Director who will join their Global R&D Quality and Compliance team. As a member of the global PV management team you will provide leadership in setting the strategic direction of Quality and Compliance PV activities. This role is suited to candidates who possess strong leadership skills and strategic thinking. Utilizing expert Good Pharmacovigilance (GVP) and Good Clinical Practice (GCP) knowledge. The su...

Location: Dublin,
Director, Pharmacovigilance Quality & Compliance (GVP)
Dublin Not Disclosed

Associate Manager (Technical Training)

Our client is a Global Biopharma based in Limerick. They are currently seeking an Associate Manager for their Technical Training who will focus on Instructional Design. This organistaion seeks people who are excited by a start-up environment, recognize the opportunities that this offers and want to be challenged. The successful person shall be responsible for leading instructional design within Technical Training, managing the eLearning program, training delivery standards, incorporating emerging learning techniques and technologies into the global training program. Role...

Location: Limerick,
Associate Manager (Technical Training)
Limerick Not Disclosed

Sr Associate QC

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

Location: Dublin,
Sr Associate QC
Dublin Not Disclosed

Sr Associate QC

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

Location: Dublin,
Sr Associate QC
Dublin Not Disclosed

QA Specialist

We’re currently recruiting for an exciting opportunity with an award winning pharmaceutical organization based in Cork. 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 •This position is responsible for carrying out tasks and projects related to management of Quality Assurance activities as required by Good Manufacturing Practice (GMP). These activities include Incoming material release, Batch release, Change control, Event management, Supplier qualification%...

Location: Cork,
QA Specialist
Cork Not Disclosed

Sr Associate QC (Senior)

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

Location: Dublin,
Sr Associate QC (Senior)
Dublin Not Disclosed

QA Specialist

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

Location: Cork,
QA Specialist
Cork Not Disclosed

QA Specialist

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

Location: Cork,
QA Specialist
Cork Not Disclosed

QA Specialist

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

Location: Cork,
QA Specialist
Cork Not Disclosed
Other Regulatory Affairs Jobs
Job Title Location Salary Actions
Director, PVE (Risk Management) Dublin Not Disclosed