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Search Results for Limerick
Job Title. Location Salary Actions

External Manufacturing Specialist

An External Manufacturing Specialist is required to join a leading global Biopharmaceutical organisation in Limerick. The External Manufacturing Specialist over

Location: Limerick,
External Manufacturing Specialist
Limerick Not Disclosed

Supply Chain Operations Specialist

A Supply Chain Operations Specialist is required to join a global biopharmaceutical organisation in Limerick. The Supply Operations Specialist co-ordinates deli

Location: Limerick,
Supply Chain Operations Specialist
Limerick Not Disclosed

Facilities Maintenance Director

A leading global Biopharmaceutical company based in Limerick is currently seeking a Facilities Maintenance Director. Responsible for the organization and Manage

Location: Limerick,
Facilities Maintenance Director
Limerick Not Disclosed

Indirect Sourcing Manager

An Indirect Sourcing Manager is required to join a leading Biopharmaceutical client in Limerick.The Sourcing manager will be responsible to support and assist in the development of the Category Management strategy by gathering and business unit supply needs and specifications for the In-Direct category globally. In this role you will work collaboratively with the Category Lead and business unit stakeholders to commercially & competitively assess the global supply base’s capabilities and qualifications. The Sourcing Manager owns the global supplier relationship an...

Location: Limerick,
Indirect Sourcing Manager
Limerick Not Disclosed

Senior QA Specialist

A Senior QA Specialist is required to join a leading Biopharmaceutical business in Limerick. The focus of this role is to perform and lead activities in support

Location: Limerick,
Senior QA Specialist
Limerick Not Disclosed

QA Materials Supplier Specialist

A QA Materials Supplier Specialist required to join a leading global Biopharma company in Limerick. This position is an integral part of our client’s program to assure that raw materials used in manufacturing are of the appropriate quality to facilitate the production of drug products meeting or exceeding expectations. It requires working with cross-functional teams and suppliers to resolve quality issues and assure product quality The Role Work with a global supplier quality team to continually evaluate supplier performance and respond accordingly based on triggering...

Location: Limerick,
QA Materials Supplier Specialist
Limerick Not Disclosed

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 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

Supply Chain Operations Manager

A Supply Chain Operations Manager is required to join a leading Biopharmaceutical business in Limerick. The Manager of Supply Chain Operations will be responsible for batch disposition activities. They will coordinate internal and external cross functional teams to ensure that finished goods are available to meet all clinical and commercial demands. The successful candidate must exercise strong leadership, initiative and technical expertise. They must also be able to prioritize work, learn new concepts quickly and juggle multiple tasks in a fast-paced environment. The Role; ...

Location: Limerick,
Supply Chain Operations 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

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 QA Operations Manager

Senior QA Operations Manager Our client, a growing biopharmaceutical organisation are currently hiring for a Senior QA Operations Manager to join their team. As Senior QA Ops Manager you will be responsible for all aspects of assigned QA Team, provides leadership and support to direct reports. You will provide QA oversight to ensure that drug substance manufacturing activities are compliant with Quality Assurance (QA) policies and procedures, cGMPs, SOPs, and Standard Requirement Documents. Responsibilities • Responsible for all aspects of QA Team including re...

Location: Limerick,
Senior QA Operations Manager
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