QA Validation Technical Writer

The role:QA Resources is currently recruiting for a Tech Writer on behalf of a leading medical device company based in Limerick. This is a 12-month contract and a fully remote role.Purpose:We are seeking a detail-oriented Technical Writer (Remote) to develop a comprehensive set of technical, validation, quality, and operational documents for medical device...

Job DescriptionAn exciting opportunity has arisen to work on a major expansion project based in Ireland. This role involves working as a technical writer, focusing on Deviation and investigation writing, Validation specifically CIP/SIP and continuing validation.Key Responsibilities:Experience in Deviation and investigation writingExperience in Validation...

Social network you want to login/join with:Technical Writer Cleaning Validation, LimerickClient: Quanta part of QCS StaffingLocation: Limerick, IrelandJob Category: OtherEU work permit required: YesJob Reference: 3caf12aa5dd1Job Views: 4Posted: 03.06.2025Expiry Date: 18.07.2025Job Description:Technical Writer Cleaning Validation - Limerick - 12-Month...

Technical Writer Cleaning Validation - Limerick - 12-Month Contract Ireland is a hive of activity for the Life Sciences Sector at present with global players setting up new and expanding existing manufacturing facilities all over the Country. An exciting opportunity has arisen to work via Quanta on the client's side for a global Pharmaceutical...

PE Global is currently recruiting for numerous QA Cleaning Validation Engineers on behalf of a leading biotech company based in Limerick. This is an initial 12 month contract role.Responsibilities:Execution of cleaning validation protocols.Working closely with manufacturing to ensure the CIP/SIP and dirty holds are to the correct times and samples are...

Job Opportunity: Technical Writer for Validation and Deviation WritingAbout the Role:Assist in administrative tasks, such as organizing documents and managing correspondence.Contribute to projects and provide general support.Answer phone calls and manage communication with stakeholders.Requirements:A willingness to learn and adapt quickly.Good communication...

The role of a Technical Writer in Medical Device DevelopmentWe are seeking a detail-oriented Technical Writer to develop comprehensive technical, validation, quality, and operational documents for medical device development and regulatory submission.Create, edit, and finalize technical and regulatory documents throughout the device lifecycle.Collaborate with...

Job Overview">A Validation Technical Writer is required to work on a 12-months contracting position with our client in the biotech industry.">Key Responsibilities">">Generation of summary reports and documents related to deviations and GMP.">Maintenance and updates of cleaning/SIP validation plans.">Scheduling of cleaning/SIP activities with manufacturing...

Job SummaryWe are seeking a highly skilled and experienced QA Validation Technical Writer to join our team in Limerick, Ireland. As a key member of our operations team, you will be responsible for executing validation protocols, writing and approving technical documents, and generating reports.About the RoleExecute SIP/cleaning and continuing validation...

Quality Assurance and Compliance SpecialistThis role requires a Quality Assurance and Compliance Specialist to oversee the Validation department's adherence to regulatory requirements. The successful candidate will ensure that processes are in place to guarantee compliance and support the implementation of company manufacturing standards policies and...