Computer System Validation Specialist

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...

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...

QA Systems and Validation Specialist(12 month Contract)Location: Swords CampusABOUT USSK biotek Ireland, an SK pharmteco company, is a global Contract Development and Manufacturing organisation (CDMO) with state-of-the-art facilities in Korea, US, France and Ireland. We are part of the wider SK Inc. with revenues of $95 billion in 2020. Our mission is to...

QA Systems and Validation Specialist(12 month Contract)Location: Swords Campus,ABOUT US?SK biotek Ireland, an SK pharmteco company, is a global Contract Development and Manufacturing organisation (CDMO) with state-of-the-art facilities in Korea, US, France and Ireland. We are part of the wider SK Inc. with revenues of $95 billion in 2020. Our mission is to...

QA Systems and Validation Specialist(12 month Contract)Location: Swords CampusABOUT US?SK biotek Ireland, an SK pharmteco company, is a global Contract Development and Manufacturing organisation (CDMO) with state-of-the-art facilities in Korea, US, France and Ireland. We are part of the wider SK Inc. with revenues of $95 billion in 2020. Our mission is to...

Cpl in partnership with SK pharmteco are looking for QA Systems and Validation Specialist on a 12 month Contract to join the team in the Swords Campus.ABOUT US?SK pharmteco company, is a global Contract Development and Manufacturing organisation (CDMO) with state-of-the-art facilities in Korea, USA, France and Ireland. We are part of the wider SK Inc. with...

Cpl in partnership with SK biotek are looking for QA Systems and Validation Specialist on a 12 month Contract to join the team in the Swords Campus.ABOUT US?SK biotek Ireland, an SK pharmteco company, is a global Contract Development and Manufacturing organisation (CDMO) with state-of-the-art facilities in Korea, US, France and Ireland. We are part of the...

Welcome to Oleson's Technology Strategy & Transformation PracticeWe are uniquely focused on IT/OT systems in manufacturing operations with a particular strength in regulated life sciences manufacturing. Our strength lies in taking a full system view and understanding the complex relationships between manufacturing operations, business continuity, IT...

About the RoleWe are seeking a highly skilled professional to fill the position of Pharmaceutical Validation Expert at DPS Group Global. The successful candidate will be responsible for leading the validation of computer systems, ensuring compliance with regulatory requirements, and collaborating with various functions on site.Key Responsibilities:Validate...

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...

Cpl Healthcare is looking for a seasoned Validation Specialist Lead to join their team. In this role, you will be responsible for ensuring the quality and compliance of our pharmaceutical products by leading projects related to computer system validation, data integrity, and change control.About the RoleYou will assess changes for GMP compliance and...

QA Systems and Validation Specialist (12 month Contract) Location: Swords Campus,ABOUT US SK biotek Ireland, an SK pharmteco company, is a global Contract Development and Manufacturing organisation (CDMO) with state-of-the-art facilities in Korea, US, France and Ireland.We are part of the wider SK Inc. with revenues of $95 billion in 2020.Our mission is to...

**About the Role**">This is an exciting opportunity to join NNIT Ireland as a Technical Validation Specialist.As a Technical Validation Specialist, you will be responsible for managing and coordinating validation activities across various equipment solutions within our regulated Pharma environment. Your key responsibilities will include drafting...

About the Job:">This is an exciting opportunity to work as a QA Systems & Validation Specialist with Cpl Healthcare. You will be responsible for providing expert guidance on quality systems, validation, and regulatory compliance. Your primary focus will be on ensuring that our quality systems meet the highest standards, adhering to relevant regulations and...

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...

Position Description:The QA Systems and Validation Specialist will be responsible for:Assessment of changes for GMP compliance in accordance with site change control procedure for facilities, utilities, lab and manufacturing equipment and control system changes.Review and approve the GMP design aspects of major capital projects including new facility...

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...

Cleaning Validation Specialist - Pharmaceuticals - 12 Month Contract - Dublin Are you looking for the chance to join a life changing pharmaceutical organisation in their mission to continuously drive innovation? We are recruiting for a Cleaning Validation Specialist for a 12-month contract based in Dublin. Located 15 minutes from Dublin Airport and...

Job DescriptionWe are seeking a customer-focused, highly motivated, and technical IT Specialist to join our IT Store & Customer team. The successful candidate will be responsible for store and retail systems used in over 220 stores across the island of Ireland.Keep the POS systems and customer-facing solutions running smoothly in our stores.Manage new store...