Equipment Qualification and Validation Lead

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...

RequirementsTo be successful in this role, you should have a Science/Engineering Degree and 3 years plus relevant validation experience in a GMP environment. Experience in executing multiple projects and participating on cross-functional project teams is essential.Additionally, you should have organizational skills for concurrent execution of multiple...

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...

Are you an experienced professional looking for a new challenge in the field of validation and qualification? Next Generation Recruitment is currently hiring an Engineering Specialist (Validation) to join a leading biopharmaceutical company at their state-of-the-art facility.About the Role:The successful candidate will be responsible for executing 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...

Job OverviewOleson is a technology strategy and transformation practice uniquely focused on IT/OT systems in manufacturing operations with a particular strength in regulated life sciences manufacturing. Our team of experts provides strategic advice or specific implementation services to deliver successful projects.We have developed our own knowledge and...

Mason Alexander has partnered with a leading pharmaceutical company in Wicklow to fill a permanent Validation Engineer position.This is a great opportunity for you to join our Quality & Regulatory team, focusing on performing and executing validation and qualification duties for all projects across the site.As a Validation Engineer, your key responsibilities...

Role Brief:The successful candidate will focus on the validation activities for a range of equipment solutions within a regulated Pharma environment. You will have responsibility for a number of activities and pieces of equipment while also supporting the wider Validation function and ensuring Validation activities are closed out in line with the Validation...

Role Brief:The successful candidate will focus on the validation activities for a range of equipment solutions within a regulated Pharma environment. You will both have responsibility for a number of activities and pieces of equipment while also supporting the wider Validation function and ensuring Validation activities are closed out in line with the...

About the RoleThis is an excellent opportunity to work on leading technologies in the biotech industry. We are looking for a skilled Biopharmaceutical Equipment Validator to join our team in Dublin.Key ResponsibilitiesPlan and execute equipment qualification and maintenance programs to ensure compliance with cGMP regulations.Develop and implement technical...

CPL's partnership with Pfizer requires a dedicated QC Equipment Validation Specialist to join their team at Grange Castle in Dublin. This 12-month fixed-term contract involves onsite work and presents an excellent opportunity for individuals interested in a dynamic and fast-paced environment.Key Responsibilities:Support the qualification of new...

Cpl in partnership with our client Pfizer are seeking a QC Equipment Validation Specialist to join the team at their state of the art site in Dublin, Grange castle for a 12 month fixed term contract.This is an onsite role.Job Purpose: Working as part of the QC Laboratory Equipment Validation Team you will be responsible for the qualification of new...

**About Our Company**The Briggs Equipment Group provides asset management and maintenance solutions across the UK and Ireland, with a focus on delivering exceptional service and support to customers.We are seeking skilled Equipment Technicians to join our Engineering team, providing opportunities for experienced professionals to work in a dynamic workshop...

The successful candidate will be responsible for executing all aspects of Laboratory Equipment Validation, including qualification of new instruments, periodic review of instrument qualification packages, routine QC support, and administration of Laboratory Computerized Systems.Key responsibilities include:New instrument and equipment validation (URS, IQ,...

Job Description: QA Validation LeadThe successful candidate will be responsible for:Qualifying computer systems and equipment in accordance with GMP guidelines.Evaluating changes for GMP compliance, including assessment of facilities, utilities, lab, and manufacturing equipment control system changes.Leading laboratory equipment validation and new product...

Key ResponsibilitiesThe primary responsibility of the Validation Engineer is to perform day-to-day tasks related to RTL design, debugging, good manufacturing practice (GMP), validation, and functional verification. This includes generation and execution of validation protocols and reports, leading and/or supporting validation projects and activities on site,...

​ Validation Lead   M/F (29380) At Guerbet, we build lasting relationships so that to enable people to live better. This is Our Purpose. We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals, medical devices, digital and AI solutions, for diagnostic and interventional imaging. As a pioneer in the...

Cpl in partnership with our client Pfizer are seeking a QC Equipment Validation Specialist to join the team at their state of the art site in Dublin, Grange castle for a 12 month fixed term contract. This is an onsite role. Job Purpose:Working as part of the QC Laboratory Equipment Validation Team you will be responsible for the qualification of new...

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...

As a Validation Engineer at Team Horizon, you will play a crucial role in ensuring the quality and reliability of our products. This exciting opportunity involves supporting our new syringe filling line project, working closely with our cross-functional teams to ensure seamless execution.">Key ResponsibilitiesDevelop, execute, review, and approve CQV test...