QC Systems Validation Engineer

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...

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...

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...

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...

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...

The role of a Validation Engineer is pivotal in ensuring the seamless integration and operation of technology systems within GxP environments.At Validation Associates LLC, we are seeking a talented professional to join our team as a Validation Engineer.This position offers an exceptional opportunity to work with our blue-chip multinational clients within the...

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...

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...

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...

Senior Validation Engineer12 month contractOn site CarlowAMC22531Start date ASAPI am looking for an experienced Equipment Validation Engineer to support the transition of a new biomanufacturing facility from project phase to a fully operational manufacturing facility.This role would be suitable for a CQV/lead Engineer with 6+ years experience in Vial and...

AMC1234Senior QC AssociateContract – 12 monthsDublinWould you like to join a leading biopharmaceutical company in Dublin to further develop your career? This is an excellent opportunity to work on leading technologies in the biotech industry. As a QC Senior Associate, you will be responsible for planning, executing, and documenting the qualification,...

Cpl in partnership with our client Pfizer are Seeking a QA Validation Specialist to join the team at their state of the art Dublin, Grange Castle Plant for an 11 month fixed term contract with Hybrid working model.Role:To provide a compliance overview of sitewide validation activities. To provide technical QA support to the Engineering function (including...

About the RoleCPL is partnering with SK biotek to recruit a QA Systems and Validation Specialist for a 12-month contract. The successful candidate will join the quality team at the Swords Campus and report directly to the Quality Manager.Key ResponsibilitiesAssess changes for GMP compliance in accordance with site change control procedures for facilities,...

Process Validation Engineer - Pharmaceuticals - Dublin - 12-Months ContractAre you a Process Validation Engineer and wanting to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? QCS Staffing's client is a global healthcare company specialising in delivering lifesaving medicines...

About the CompanySK 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. Our mission is to 'make what matters for a healthy, happier world', from grams to tonnes.The OpportunityWe are seeking a QA Systems and Validation Specialist to...

AMC1234 Senior QC Associate Contract – 12 months DublinWould you like to join a leading biopharmaceutical company in Dublin to further develop your career?This is an excellent opportunity to work on leading technologies in the biotech industry.As a QC Senior Associate, you will be responsible for planning, executing, and documenting the qualification,...

QC Specialist Data AnalyticsTeam Horizon is seeking a QC Specialist Data Analytics for our client based in Dublin who will have a key role in Quality Transformation and the QC Optimization Initiative. The role will be responsible for applying advanced data analytics to extract actionable insights, optimize QC workflows, and drive digital transformation in...