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
Alert

Sorry
There are no Open Vacancies that Match your Search

Please explore current open vacancies in the box below
Search Results
Job Title. Location Salary Actions

Project Manager UDI

A Project Manager UDI is required to join a leadingMedical Device organisation. This role is International and will require 15% travel . Your role: As the Project Manager (UDI – Unique Device Identification) you will be responsible for supporting the implementation of GS1 standards which lead to maintaining regulatory and commercial compliance and approval for the company’s products in International Region. Your responsibilities: Complete or assist with implementation of GS1 standards and UDI requirements in collaboration...

Location: Republic of Ireland,
Project Manager UDI 		Republic of Ireland Not Disclosed

Regulatory Affairs Manager (EMEA)

A Regulatory Affairs Manager (EMEA) is required to join a leadingMedical Device organisationin Athlone . Your role: As the Regulatory Affairs Manager you will be responsible for determining and supporting the regulatory activities which lead to, and maintain regulatory compliance and approval for company products globally. Your responsibilities: Primary responsibility for regulatory affairs in the EMEA region. Pursue relevant information pertaining to new developments in regulatory affairs by maintaining contact w...

Location: Roscommon,
Regulatory Affairs Manager (EMEA) 		Roscommon Not Disclosed

Regulatory Affairs Project Leader

We’re currently recruiting for an exciting opportunity with an award-winning Medical Device organization based in Cork . The Regulatory Affairs Project Leader is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Your duties: As the Regulatory Affairs Project Leader, you will serve as a technical expert on Regulatory Affairs matters and will be responsible for providing assistance in the preparation and submission of global regulatory documents with little to no supervision. You may act as a team le...

Location: Cork,
Regulatory Affairs Project Leader 		Cork Not Disclosed

NPD Project Manager (Healthcare)

NPD Project Manager Our client is a leading Healthcare company, based in Dublin. Reporting to the New Product Development (NPD) Director, the NPD Projects Manager will give full support to the delivery of NPD projects. The New Product Development Projects Manager supports and interacts within a team dedicated to developing and creating meaningful and lasting solutions that patients can understand and identify with. As an important member of the NPD team, the Product Development Projects Manager is responsible for assisting in the work-flow for the development of multiple proje...

Location: Dublin,
NPD Project Manager (Healthcare) 		Dublin Not Disclosed

Clean Utilities Engineer

The Clean Utilities Engineer will perform an integral role in the development of the company. You will take ownership for the clean utilities (such as, but not limited to, Water for injection, clean steam, clean dry air, nitrogen) and the clean utilities equipment. You will provide leadership, cross functional support and technical expertise to IUFT, maintenance and manage their operation through design, construction, validation, start-up and commercial manufacturing. Ensure that objectives are effectively achieved, consistent with the company’s requ...

Location: Carlow,
Clean Utilities Engineer 		Carlow Not Disclosed

Scientific Communications Publication Capability Lead

Our client, a global pharmaceutical organisation are currently recruiting for a Scientific Communications Publication Technical Advisor to join their team. As Publication Capability Lead you will help drive launch and publication capabilities and operational excellence for the Global Scientific Communications Group. Responsibilities Function as an expert on the publication medical writing, publication processes and practices, including authorship, transparency and ethics Consults and advise site publication writers on issue management and escalation Represent the gro...

Location: Cork,
Scientific Communications Publication Capability Lead 		Cork Not Disclosed

Regulatory Scientific Communications Associate

Our client, a global pharmaceutical organisation are currently recruiting for a Scientific Communications Associate to join their newly created Global Scientific Communications team. As Regulatory Scientific Communications Associate you will work with cross-functional, multidisciplinary teams to lead the development of documents intended for regulatory audiences including, clinical study reports, briefing documents, regulatory responses, Investigational New Drug Applications, and marketing authorization applications. Responsibilities Document Preparatio...

Location: Cork,
Regulatory Scientific Communications Associate 		Cork Not Disclosed

GMP Inspector (Compliance )

Our client, based in Dublin city centre, requires a GMP Inspector to join their team. This is a 3 year Fixed Term Contract. Reporting to a Senior Inspector, the Inspector will be primarily responsible for assessing the compliance of manufacturers with EU Good Manufacturing Practice (GMP). The role of an Inspector is to evaluate the compliance of sites inspected, in Ireland & abroad, with the requirements of National legislation (in Ireland), European Community Directives, Regulations and Guidance. These sites may include; o Manufacturers & distribu...

Location: Dublin,
GMP Inspector (Compliance ) 		Dublin Not Disclosed

Senior Regulatory Compliance 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 supporting tasks and projects related to management of Regulatory Compliance and new product submissions •These activities include QA/Compliance support for worldwide submissions of new drug applications and post approval changes, change control support, manufactu...

Location: Cork,
Senior Regulatory Compliance Specialist 		Cork Not Disclosed

Regulatory & Claims Officer

Role Overview: This role is responsible for product registration and document control across all global brands and markets. The position requires significant organisation skills, with cross functional engagement to ensure relevant documents are supplied on time and to a high standard. Role Deliverables: Register products for new markets, maintain and submit necessary documentation to local regulatory agencies and ensure continued licence to operate for brands. Manage technical standards and support regulatory product compliance across all bra...

Location: Louth,
Regulatory & Claims Officer 		Louth 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

Scientist Data Analytics

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 • The Data Analyst will contribute to development of Automated reports and Visualizations. Specifically, the Scientist will create statistical models and visualizations that integrate many types of data to create comprehensive models. Models will then be applied to determine stability of Product and ...

Location: Cork,
Scientist Data Analytics 		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

Supplier Quality Auditor (Pharmaceutical)

Our client is based in Cork and are a leading international supplier of generic pharmaceutical drugs. Their products are manufactured at established facilities that are registered with the U.S. Food and Drug Administration (FDA). Our clients generics portfolio is broad and continues to meet the wide-ranging, ever-growing needs of its customers. As a member of the auditing team the post holder will be responsible for assisting the Auditor Manager in ensuring that licensed pharmaceutical products are manufactured, tested and released in compliance with cGMP, US FDA and other applic...

Location: Cork,
Supplier Quality Auditor (Pharmaceutical) 		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

Senior Associate Regulatory Affairs

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

Location: Dublin,
Senior Associate Regulatory Affairs 		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

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
Subscribe RSS feed for this search