Validation and Qualification Professional

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...

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...

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...

We are looking for a highly skilled Equipment Qualification and Validation Lead to join our team in Dublin. As part of the QC Laboratory Equipment Validation Team, you will be responsible for the qualification of new instrumentation, modernization of existing equipment, and facility modification or expansion projects within the QC Laboratories.Key...

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...

What We Offer">Demonstrated strong Communication and Leadership skills.Demonstrated ability to collaborate with senior stakeholders to achieve optimal outcomes.Strong understanding of a risk-based approach to commissioning and qualification within the biotechnology industry.">About Us">Recruitment By Aphex Group is committed to delivering exceptional talent...

Job TitleWe are seeking a senior-level Senior Validation Professional to join our team. In this role, you will play a key part in ensuring that all aspects of validation are performed to the highest standards.About the RoleYou will be responsible for leading technical projects, including designing, documenting, and executing qualification/validation...

Commissioning and Qualification Expert WantedTandem Project Management Limited is a dynamic biotech start-up in South Dublin, dedicated to pioneering cutting-edge bioprocessing technology. We are seeking an experienced CQV Engineer to lead our commissioning and qualification efforts.Responsibilities:Lead CQV activities for small-scale bioprocessing...

Role OverviewThis is an exciting opportunity for a Pharmaceutical Validation Professional to join our team at TN Ireland. The successful candidate will be responsible for supporting various aspects of validation, including sterilization, cleaning, and controlled temperature units.Main ResponsibilitiesDevelop and execute qualification and validation...

The role of QC Equipment Validation Specialist with CPL is a critical component of our partnership with Pfizer at their site in Dublin. This 12-month fixed-term contract offers an exciting opportunity for professionals to contribute to the success of this project.Main Duties:Support the qualification of new instrumentation and modernization of existing...

We have partnered with a prominent pharmaceutical company based in Ireland to fill a permanent Validation Engineer position.The ideal candidate will join a dynamic team as part of the Quality and Regulatory function, focusing on delivering validation and qualification services for all projects across the site.Your key responsibilities will include:Protocol...

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,...

Job DescriptionCpl Healthcare, in partnership with our client Pfizer, are seeking an experienced Cleaning Validation Specialist to join their team for a fixed-term contract at their state-of-the-art facility.The successful candidate will be responsible for supporting new product introduction and cleaning validation activities across the site. This role is...

As a Validation Specialist at Viatris, you will have the opportunity to make a significant impact on the development and implementation of our process validation and qualification strategies. This role is ideal for individuals who are passionate about quality assurance and have a strong background in validation engineering.The Job DescriptionThis role...

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...

About the OpportunityWe are offering an exciting opportunity for a GMP Validation Engineer to join our team at Orion Group Life Sciences. As a key member of our engineering department, you will play a crucial role in ensuring the quality and compliance of our biopharmaceutical products.Key ResponsibilitiesDesign and Development: Create and execute...

Job Title: Verification and Validation ProfessionalCpl Healthcare is seeking a highly skilled Verification and Validation Professional to join our team. As a Content Moderator, you will be responsible for content clarification and verification of business contact details. This involves making outbound phone contact with clients in a courteous and...

Cpl Healthcare is committed to delivering high-quality medical devices that meet the needs of patients and healthcare professionals. We are seeking a skilled Validation Engineer to join our team and contribute to the development of our products.About the RoleThis is an exciting opportunity for a qualified Validation Engineer to take on a challenging role...