GxP Validation Specialist

Overview of the JobWe are seeking a skilled Validation Specialist to join our team in DPS Group Global. As a CSV Specialist, you will be responsible for managing the validation of GxP computerized systems, ensuring compliance with regulatory requirements and maintaining data integrity.Your key responsibilities will include:Project management and execution of...

Requirements and ResponsibilitiesWe are looking for a highly skilled and experienced CSV Specialist to join our team in DPS Group Global. The ideal candidate will have extensive experience working in a GMP environment and knowledge of validation requirements relating to GxP computerized systems.The successful candidate will be responsible for:Project...

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...

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 DescriptionAbout the RoleThe CSV (Computer System Validation) Specialist will manage the validation of GxP computerized systems, including the preparation of validation documentation and execution of required testing.This role is responsible for project management and execution of qualification activities related to GxP computerized system validation....

Get AI-powered advice on this job and more exclusive features.Recruitment Specialist @ Arcadis DPS GroupCSV SpecialistPurpose and Scope:Reporting to the Lead, Pharma Manufacturing Quality Services Dublin, the CSV (Computer System Validation) Specialist will manage the validation of GxP computerized systems, including the preparation of validation...

About this JobThis Mid-Senior level position is part of the Information Technology and Project Management team in DPS Group Global. As a CSV Specialist, you will be working on the validation of GxP computerized systems, which includes the preparation of validation documentation and execution of required testing.Key responsibilities include:Project management...

Job Summary: We are seeking a highly skilled Automated Validation and Qualification Specialist to join our team. In this role, you will be responsible for developing validation strategies, creating validation output documents, and ensuring compliance with regulatory requirements. This position requires a strong understanding of computer system validation...

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...

Hobson Prior is collaborating with a Biotech company who are in search of a Specialist in QA Validation. The chosen individual will offer supervision for the production and distribution of Gene Therapy medicinal products. They will be instrumental in guaranteeing that processes and equipment meet validation and qualification standards as per relevant...

Company OverviewWarman O'Brien is a leading provider of IT solutions to the pharmaceutical manufacturing and biotechnology research industries.We are committed to delivering high-quality products and services that meet the strict regulations of our clients.As a Senior Validation Engineer, you will play a critical role in ensuring that our IT applications are...

We're currently recruiting for an exciting opportunity with a Pharmaceutical organization based in Carlow. 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.DutiesExecute cleaning cycle development and PQ of equipment.Writing and adhering to validation strategies, coordinating with...

Required Skills and QualificationsTo be successful in this role, you will need:At least 10 years of experience in software validation and SQA.Proficiency in GxP regulations, validation principles, and automated testing.Experience with Salesforce, Veeva, and tools like JIRA, Tosca, ALM, and Confluence.Knowledge of Agile and Waterfall methodologies.

Job Description: We are seeking a highly skilled Validation & CSV Lead Engineer to join our team. As a key member of our engineering department, you will be responsible for guiding the development of the master validation plan, creating validation strategies, and overseeing the creation of validation output documents. This role requires a deep understanding...

Exciting Opportunity with a Pharmaceutical OrganizationWe're currently recruiting for an exciting opportunity with a Pharmaceutical organization based in Carlow. 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.DutiesExecute cleaning cycle development and PQ of equipment.Writing...

About Our ClientOleson is a specialist provider of consultancy and implementation services for IT infrastructure and data architectures within life science manufacturing. We take a full system view, understanding the complex relationships between manufacturing operations, business continuity, IT infrastructure, compliance & change control, and system...

Company OverviewThe Rovisys Company is a leading provider of validation services to the pharmaceutical, biotechnology, and medical device industries. Our team of experts works closely with clients to ensure compliance with regulatory standards and drive business growth.We are seeking an experienced and motivated Validation leader to develop and lead a...

Direct message the job poster from Warman O'BrienPractice Lead - Regulatory Affairs at Warman O'BrienSenior Validation Engineer12-month freelance contractOnsite in Dublin40 hours/week€50 per hour maximum payOverview:Seeking an experienced CSV professional to ensure compliance and quality of SDLC deliverables for regulated IT...

Job Overview\We are seeking a highly skilled and experienced Senior Validation Engineer to join our team at Eir Evo Talent. The successful candidate will have a strong background in automation process validation, with a focus on CSV (Computer System Validation) methodologies.\The ideal candidate will be responsible for leading the overall validation &...

Job Description\This is a unique opportunity to join Eir Evo Talent as a Lead Validation Engineer for medical devices. The successful candidate will have extensive experience in process/equipment validation, with a strong understanding of CSV (Computer System Validation) methodologies.\The ideal candidate will be responsible for guiding the team in creating...