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 Limerick
Job Title. Location Salary Actions

Quality Compliance Specialist

A Quality Compliance Specialist QRM is required to join a leading global biopharmaceutical organisation in Limerick. This role supports the work of our client’s Industrial Operations and Product Supply (IOPS) site through the use of quality risk management (QRM) principles and techniques. The scope may also include collaboration with other IOPS Sites, partners, CMOs and their respective programs. The Role Ensuring compliance with all aspects of the QRM program Provide advice on all QRM matters within the IOPS organization Facilitate risk assessments Res...

Location: Limerick,
Quality Compliance Specialist
Limerick Not Disclosed

Associate Director QA Medical Devices

Our client a multinational biotech company and currently seeking an Associate Director of QA for their Medical Device/Combination Products. The Associate Director will Provide QA oversight of the Medical Device/Combination Products including pre-filled syringe and auto-injectors/pen injectors for biological therapeutics developed in-house and in collaboration with partners and CMO’s. Supports the work of Industrial Operations and Product Supply (IOPS) sites through the use of quality risk management principles and their application to medical device development and comme...

Location: Limerick,
Associate Director QA Medical Devices
Limerick Not Disclosed

Design Control Engineer

In this role with a leading medical device company, you will develop and refine Global Design Controls, Process Development, and Risk Management quality system policies and procedures for new product development (NPD). Ensure quality system policies and procedures meet the needs of stakeholders and the expectations of regulators, in particular: • Ensure the policies and procedures are compliant with applicable standards, regulations, and guidance documents. • Interpret standards, regulations, and guidance documents to tailor these needs into systems ...

Location: Limerick,
Design Control Engineer
Limerick Not Disclosed

Associate Director Quality Risk Management System

Associate Director Quality Risk Management System Our client, a leading biotech organisation are currently recruiting for an Associate Director Quality Risk Management System. As Associate Director Quality Risk Management System you will be global process owner of the end to end Global Quality Risk Management System across global functions at sites, including combination product development, Drug substance and drug product clinical and commercial production. You will be responsible for ensuring adoption of Risk Management principals is applied across disciplines and lifecycle throu...

Location: Limerick,
Associate Director Quality Risk Management System
Limerick Not Disclosed

Senior GMP Auditor

Consistently ranked as a “Top Employer” in Science Magazine’s rankings for pharmaceutical and biotechnology companies, our client offers a unique, world-class opportunity for interested candidates. An outstanding Senior GMP Auditor is required who is excited by a start-up environment and recognizes the opportunities that this offers and wants to be challenged Summary:Responsible for planning and conducting quality audits in manufacturing (GMP) within designated Quality Auditing area. Responsibilities Schedules, prepares, an...

Location: Limerick,
Senior GMP Auditor
Limerick Not Disclosed

Technical Writer

We’re currently recruiting for an exciting opportunity with an award-winning medical device organization based in Limerick . 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 Position Description and Responsibilities Perform technical writing, research, and related editing functions to prepare documents, test plans, user cases, project manuals, business proposals, reports, briefings, presentations, guidelines, and other written materials. Technical Pr...

Location: Limerick,
Technical Writer
Limerick Not Disclosed

Senior Quality Engineer

Senior Quality Engineer The Senior Design Assurance Engineer is accountable for quality support for products developed and process design to achieve these goals through active participation and contribution to multifunctional and multi-divisional teams. The Senior Design Assurance Engineer is responsible for assuring that quality standards and regulatory compliance activities are consistent with Corporate/Division Policies, Government Regulations, International Standards and standards broadly recognized by the Medical Device Industry. The position requires a self-motivated, self-d...

Location: Limerick,
Senior Quality Engineer
Limerick Not Disclosed

QA Validation Manager

QA Validation Manager Our client, a large biopharmaceutical organisation are currently recruiting for a QA Validation Manager to join their team on a permanent basis. As QA Validation Manager you will be responsible for implementing policies and procedures to validate/qualify equipment, systems, and processes in accordance with regulatory requirements and the organisations manufacturing standards, and will manager a team of Validation Specialists. Responsibilities • Manage, develop and build a team of subject matter experts in the areas of cleaning validation and...

Location: Limerick,
QA Validation Manager
Limerick Not Disclosed

Senior GMP Auditor

Consistently ranked as a “Top Employer” in Science Magazine’s rankings for pharmaceutical and biotechnology companies, our client offers a unique, world-class opportunity for interested candidates. An outstanding Senior GMP Auditor is required who is excited by a start-up environment and recognizes the opportunities that this offers and wants to be challenged Summary:Responsible for planning and conducting quality audits in manufacturing (GMP) within designated Quality Auditing area. Responsibilities Schedules, prepares, an...

Location: Limerick,
Senior GMP Auditor
Limerick Not Disclosed