Validation Specialist for Pharmaceutical Manufacturing

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...

About the RoleThis Pharmaceutical Validation Professional position offers an excellent opportunity to work with an award-winning organization based in Dublin.The successful candidate will provide technical expertise in validation activities, ensuring compliance with regulatory requirements.Key ResponsibilitiesThe role involves validation oversight of...

Cleaning Validation Specialist - Pharmaceuticals - 12 Month Contract - DublinAre 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 just a...

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...

Cleaning Validation Specialist - Pharmaceuticals - 12 Month Contract - DublinAre 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 just a...

Job OverviewWe are currently recruiting for an exciting opportunity with a leading Pharmaceutical organization based in Dublin.This is an excellent position for individuals who want to work with a multinational company known for excellence in their field.Duties and ResponsibilitiesThe Senior Validation Specialist will be responsible for providing oversight...

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...

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 life-saving and...

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...

We are looking for a skilled Maintenance Technician to join our team at DPS Group Global. As a key member of our team, you will be responsible for ensuring the optimal performance and reliability of all equipment and systems within the pharmaceutical manufacturing facility.This is a mid-senior level position that requires strong analytical and...

Aseptic Manufacturing Validator PositionWe are seeking an experienced Aseptic Manufacturing Validator to join our team.The role involves providing technical expertise in validation activities, ensuring compliance with regulatory requirements.Main ResponsibilitiesThe Aseptic Manufacturing Validator will be responsible for validation oversight of External...

About the Role:This QA Manufacturing Analyst role is responsible for performing aseptic sampling and environmental monitoring as part of the establishment of the Environmental Monitoring programme for aseptic manufacture and water systems.Responsibilities:Performing aseptic sampling and environmental monitoringLiaising with Validation, Quality Control,...

About the RoleWe are seeking a highly skilled and motivated Manufacturing Associate to join our team at TN Ireland. As a global biologics manufacturer, we have a strong focus on quality and excellence in everything we do.The successful candidate will be responsible for filling pharmaceuticals in accordance with cGMP regulations, setting up and operating...

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 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...

Validation and Tech Transfer Specialist (BBBH27990) Dublin, Republic of IrelandThe Validation & Tech Transfer Specialist will be responsible for developing and maintaining validation (process and cleaning validation, continued process verification) and tech transfer guidance and supporting toolkit to support implementation in a consistent manner across...

Job OverviewWe are looking for an experienced engineer to join our team and support a new syringe filling line project.The successful candidate will have extensive knowledge of pharmaceutical/biotechnology projects and experience executing validation activities.Main TasksExecute commissioning, qualification, and validation activities for pharmaceutical...

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...