close

Did you know that your Internet Explorer is out of date?

To get the best possible experience using our website we recommend that you upgrade to a newer version or download another web browser.
A list of the most popular web browsers can be found below. Just click on the icons to get to the download page.

crome
Google Chrome
IE
Internet Explorer
firefox
Mozilla Firefox
opera
Opera

Your browser will need to close to complete the installation and you will need to manually reload the site when finished
Search Results for Medical Device
Job Title. Location Salary Actions

Senior Regulatory Affairs Specialist

Would you like to join a leading medical device company in Galway, in a regulatoey affairs role? If you have previous Regulatory Affairs experience working with class III medical devices, this could be the role for you. RESPONSIBILITES Responsibilities may include the following and other duties may be assigned. Directs or performs coordination and preparation of document packages for regulatory submissions. Teams with business unit Regulatory Affair Specialists and international regulatory staffs to provide regulatory support for new products/therapies and changes to ex...

Location: Galway,
Senior Regulatory Affairs Specialist
Galway 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

Fluent Italian Medical Information Analyst

Fluent Italian Medical Information Analyst Our client, a global pharmaceutical organisation based in Cork require a fluent Italian speaker to join their Medical Information team. Fluency in English is also essential. As Medical Information Analyst you will combine your scientific knowledge and communication expertise in order to organize and deliver relevant medical communications to customers. Responsibilities Support Medical Information Services in Europe by professionally responding to medical/pharmaceutical inquiries from Health Care Providers (HCPs)%...

Location: Cork,
Fluent Italian Medical Information Analyst
Cork 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

QC Analyst HPLC

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 equipment, lab utilities and testing procedures as required by Good Manufacturing Practice (GMP). Partners with other Departments to ensure that all QC testing activities are completed in an efficient manner. &bull%...

Location: Cork,
QC Analyst HPLC
Cork Not Disclosed

Regulatory Affairs Specialist

Our client a medical device early stage company wishes to add a Regulatory Affairs Specialist to our team. The successful candidate will work with the Design, Quality and Regulatory teams to support all regulatory functions for both existing and new products. Role/Responsibilities • Contribute to the regulatory strategy plans for new products, including required Regulatory Agency approvals. • Provide regulatory input into labelling, test strategies for new product development, risk analysis, clinical, preclinical and marketing issues. • Planning,...

Location: Cork,
Regulatory Affairs Specialist
Cork Not Disclosed

Regulatory Affairs & Quality Manager

Regulatory Affairs & Quality Manager Our client a cardiovascular medical device start-up looking to hire a Quality and Regulatory Affairs manager. The succ

Location: Dublin,
Regulatory Affairs & Quality Manager
Dublin Not Disclosed