Validation and CSV Lead for Equipment Inspection

Validation & CSV Lead EngineerJob Type: PermanentLocation: Limerick, Ireland (Fully Onsite)The RoleThe validation lead should be able to guide the team in creating the master validation plan (MVP), validation strategy, and creating the validation output document (FAT, SAT, IQ OQ PQ) aligning to business SOPs. The client is seeking to validate a new machine...

Job Overview: We are seeking a seasoned CSV Lead Engineer to join our team. In this role, you will be responsible for leading the development of validation strategies, creating validation output documents, and ensuring compliance with regulatory requirements. This position requires a strong understanding of computer system validation methodologies, GxP...

Location: Ireland/ RemoteJob Summary:VEQTOR is currently looking for an Automation CSV & CQV Engineer who has demonstrable expertise in the pharmaceutical or life sciences industry and wants to get involved in ensuring the compliance and validation of critical systems. We are seeking a professional with a background in working on validated systems and...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...

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...

We are seeking a highly skilled and experienced QA Validation Lead to join our team at SK pharmteco.About UsAs a global Contract Development and Manufacturing Organisation (CDMO), we have state-of-the-art facilities in Korea, US, France, and Ireland. Our mission is to produce and deliver life-changing therapies that improve patient outcomes and save...

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...

+353-21-4834930 Specialists in Life Science Automation and IT SystemsStay Connected :SimoTech provides manufacturing automation and IT systems engineering, project management and validation services. We partner with life sciences companies to design, build, operate and optimise critical process automation systems that deliver fast track project delivery,...

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...

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...

Company OverviewDPS Group Global is a leading organization in the field of pharmaceutical development and manufacturing. We are committed to delivering high-quality products and services to our clients, while maintaining the highest standards of safety, efficacy, and compliance.Job Description:We are seeking a highly skilled Lead Validator for Pharmaceutical...

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 Validation Lead at SK pharmtecoLocation: Swords, Co DublinContract: 12 monthsABOUT USSK pharmteco 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 SK Inc., a Korea company with revenues of $99 billion in 2023. Our mission is to 'produce and deliver...

QA Validation Lead at SK pharmtecoLocation: Swords, Co DublinContract: 12 monthsABOUT USSK pharmteco 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 SK Inc., a Korea company with revenues of $99 billion in 2023. Our mission is to 'produce and deliver...

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...

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...

Cpl in partnership with The SK pharmteco Small Molecule facility located in Swords, Co Dublin, are looking for a QA Validation Lead to join the team on a 12 month contract.ABOUT US?SK pharmteco 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 SK Inc., a...

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...

Sky-high expectations are set for the ideal candidate who will take on the role of QA Systems and Validation Specialist at Cpl Healthcare's partner company, SK biotek Ireland. A 12-month contract awaits the chosen professional, with the possibility of extension.We're looking for someone with at least 3 years of pharmaceutical industry experience,...