Validation Technical Writer

Job Description A Validation Technical Writer is required by Careerwise recruitment to work with our Limerick biotech client on a 12-months contracting position. Role of this position Generation of Summary Reports. Writing and approving Deviations/ GMP documents. Maintain and update Cleaning/ SIP Validation Plan. Schedule of Cleaning/ SIP...

A Validation Technical Writer is required by Careerwise recruitment to work with our biotech client on a 12-month contracting position.Role and ResponsibilitiesGenerate Summary Reports detailing key findings and conclusions.Write, review, and approve Deviations/GMP documents ensuring compliance with regulatory requirements.Maintain and update Cleaning/SIP...

Technical Writer Cleaning Validation OpportunityIreland's Life Sciences Sector is thriving, with global players establishing new manufacturing facilities across the country. Quanta has partnered with a leading pharmaceutical organization on an expansion project in Munster region. This 12-month contract position offers a unique chance to work in a picturesque...

Technical Writer Cleaning Validation - Limerick - 12-Month ContractIreland 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 organisation on...

Technical Writer Cleaning Validation - Limerick - 12-Month ContractIreland 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 organisation on...

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...

Job Description A QA Validation Technical Writer is required by Careerwise recruitment to work with our Limerick based biotech client on a 12-month contract position. Role of this position Execution of SIP/ cleaning and continuing validation protocols. Writing and approving Deviations/ GMP documents Technical writing experience in writing site...

Technical Writer Cleaning Validation - Limerick - 12-Month ContractIreland is a hive of activity for the Life Sciences Sector at present with global players setting up new and expanding existing operations.Seniority levelEntry levelEmployment typeFull-timeJob functionMarketingPublic RelationsWriting/EditingIndustriesStaffing and Recruiting#J-18808-Ljbffr

Job DescriptionA QA Validation Technical Writer is required by Careerwise Recruitment to work with our biotech client in Limerick on a 12-month contract position. The role involves executing SIP/Cleaning and Continuing Validation Protocols, writing and approving deviations and GMP documents, technical writing experience in site reports,...

A dedicated Technical Writer is required to support our Limerick-based biotech client on a 12-month contract basis. As a key member of the team, you will be responsible for executing critical validation protocols, documenting processes, and ensuring compliance with industry regulations.ResponsibilitiesExecute complex SIP/cleaning and continuing validation...