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Search Results for Limerick
Job Title. Location Salary Actions

Facilities Compliance Specialist

Facilities Compliance Specialist Our client is a leading pharmaceutical company based in Limerick who are currently looking for a Facilities Compliance Specialist to join their team. This is a full time, permanent position with excellent salary and benefits package. Main Responsibilities: • Determine the requirement for a Deviation for Facilities Department related events. • Lead and complete investigations for the Facilities Department issues of non-compliance. • Acts as a liaison between the Facilities Department and quality and regulatory groups to define...

Location: Limerick,
Facilities Compliance Specialist
Limerick Not Disclosed

QA Specialist - External Manufacturing

A QA Specialist/ Senior Specialist - External Manufacturing is required to join a leading biopharmaceutical organisation in Limerick. The focus of the role is t

Location: Limerick,
QA Specialist - External Manufacturing
Limerick Not Disclosed

Quality Specialist

A Quality Specialist / Senior Specialist is required to join a leading global Biotechnology organisation based in Limerick. The focus of the role is to perform activities in support of dispositioning product and/or raw materials while ensuring compliance with Quality Assurance (QA) policies and procedures, cGMPs and SOPs Responsibilities Represent Quality Assurance in support of complex Deviations, Change Controls, CAPAs, etc., including active participation in investigation, evaluation, and problem resolution Train and/or mentor junior employees, in...

Location: Limerick,
Quality Specialist
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

QA Specialist - MES

AQuality Assurance Specialist MES is required to join a leading global Biotechnology organisation. This is a newly created role where you will be the lead QA representative for the recently implemented MES. You will be responsible for the review and approval of QA procedures associated with the Manufacturing Execution System. The Role Support the dispositioning of product and/or raw materials while ensuring compliance with Quality Assurance (QA) policies and procedures, cGMPs, SOPs, and Standard Requirement Documents. Work directly with the MES and Operati...

Location: Limerick,
QA Specialist - MES
Limerick Not Disclosed