CQV Validation Specialist

We are hiring for a CQV Engineer (staff consultancy role) to join our clients expanding Life Sciences division. The client's HQ is based in Dublin, and the first project is based on site in Co. Louth. Overview: You will join our high-performance team of Technical Engineers and work within an expanding team providing cutting-edge solutions to clients. You...

Role Overview:A CQV Engineer is responsible for ensuring that equipment, systems, and processes in pharmaceutical and biotechnology facilities meet regulatory and operational requirements. They play a key role in commissioning, qualification, and validation activities to ensure compliance with GMP (Good Manufacturing Practices) and other industry...

CQV Engineer- Fill Finish - Pharmaceuticals - Carlow - 12-Month ContractWith worldwide demand for their life-changing oncology treatment increasing; one of our global pharmaceutical clients is looking for a CQV Engineer to join their team to support multiple capital projects taking place onsite in Leinster.This is a fantastic opportunity to work on a...

Job Title: Commissioning, Qualification, and Validation (CQV) EngineerJob Overview: We are seeking a highly skilled and motivated Commissioning, Qualification, and Validation (CQV) Engineer to join our team. This role involves overseeing the validation and qualification of equipment, systems, and facilities within a regulated environment. The CQV Engineer...

Who We Are: At West, we're a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of...

CQV Engineer - Process Equipment 12 month contract On site - South Dublin AMC4083 Overview: I am looking for a Process Equipment Commisioning & Qualification (C&Q) engineer for various capital projects. In this role you will ensure the C&Q activities associated with various capital projects are completed safely, as per schedule and in compliance with GMP and...

A true single-source provider from concept to commercialization for biologics produced from mammalian cell culture.As CQV Engineer (Thermal Mapping) you will be responsible for thermal mapping activities for the upstream and downstream packages to enable start-up of the processing facility and for the ongoing activities during sustaining operations. The...

Summary: An exciting opportunity has arisen for a CQV (Commissioning, Qualification & Validation) Engineer to join a fast-growing biotech start-up in South Dublin. This role will be key in supporting the installation, commissioning, and qualification of small-scale bioprocessing equipment as the company scales its operations. If looking for a hands-on role...

The CQV Engineer will be responsible for the commissioning, qualification, and validation of equipment, systems, and processes used in the production of drug substances. This role ensures that all systems operate as intended and comply with regulatory standards. The CQV Engineer will work closely with cross-functional teams, including engineering, quality...

The CQV Engineer will be responsible for the commissioning, qualification, and validation of equipment, systems, and processes used in the production of drug substances. This role ensures that all systems operate as intended and comply with regulatory standards. The CQV Engineer will work closely with cross-functional teams, including engineering, quality...

Role OverviewWe are seeking a highly skilled Validation Associate to join our team. As a key member of our technology strategy & transformation practice, you will play a crucial role in ensuring the quality and compliance of our clients' IT/OT systems.About UsOleson is a specialist provider of consultancy and implementation services for IT infrastructure and...

The ultimate purpose of technology teams in GxP environments is to serve the evolving needs of the business. We are a specialist provider of consultancy and implementation services for IT infrastructure and data architectures within life science manufacturing. Our role is to be a companion on the road for technology teams to be able to use as a tool at times...

Main ResponsibilitiesManaging the workload and providing coaching for a team of Validation Engineers within the assigned area working on;Aligning new facility introduction with Validation approach across Carlow site and review and approval of project VMP;CQV approver for C&Q documents and input to Validation strategy documents and project plans and...

Job SummaryTandem Project Management Limited is seeking a highly skilled CQV Engineer to join our team. As a key member of our biotech start-up, you will play a critical role in supporting the installation, commissioning, and qualification of small-scale bioprocessing equipment.Key Responsibilities:Develop and execute CQV protocols in compliance with...

RequirementsTo be considered for this role, you should have:A minimum of 6 years of experience in CQV/QA/QC/Validation in a highly regulated industry.A minimum of 2 years of process equipment CQV/QA/Validation experience on Greenfield/Brownfield, Large Scale Project, or new facility introduction.Expertise in Equipment Qualification on cleaning and parts...

About the RoleThis is a key opportunity for a skilled CQV/lead Engineer with 6+ years experience in Vial and Syringe Filling operations to join our team.The successful candidate will be involved in the project from Operational Qualification (OQ) through to the Equipment Performance Qualification, Validation and Product PQ – including filing with regulatory...

Senior Validation Engineer12 month contractOn site CarlowAMC22531Start date ASAPI am looking for an experienced Equipment Validation Engineer to support the transition of a new biomanufacturing facility from project phase to a fully operational manufacturing facility.This role would be suitable for a CQV/lead Engineer with 6+ years experience in Vial and...

Senior Validation Engineer12 month contractOn site CarlowAMC22531Start date ASAPI am looking for an experienced Equipment Validation Engineer to support the transition of a new biomanufacturing facility from project phase to a fully operational manufacturing facility.This role would be suitable for a CQV/lead Engineer with 6+ years experience in Vial and...

CQV Lead Engineer - North of Ireland - 12 Months ContractDo you want to be part of one of the top 10 best companies to work for in Ireland? We have a superb opportunity for a Manufacturing Biotech Associate to join our client, a global pharmaceutical organisation in their new multifunctional facility.Essential Duties and Responsibilities for this role...

CQV Lead Engineer - North of Ireland - 12 Months ContractDo you want to be part of one of the top 10 best companies to work for in Ireland? We have a superb opportunity for a Manufacturing Biotech Associate to join our client, a global pharmaceutical organization in their new multifunctional facility.Essential Duties and ResponsibilitiesFor this role...