Csv validation engineer jobs in Cashel, Co. Tipperary

 ...Job Spec for QA Validation Contract Contract for 6-12 months. Role is mostly on site – could be scope for small amount remote,...  ...Project validation plans. · Co-ordinates with manufacturing / engineering personnel for respective Qualification / Validation / Re-... 

 ...QA Validation Specialist Equipment Utilities 6 mth contract Summary : QA Validation role...  ...and procedures. Support to production / engineering to ensure the qualified state of...  ...validation and computerized system validation (CSV) activities including data integrity compliance... 

 ...QA Validation Specialist Lab 6 mth contract Summary : QA Validation role to ensure Qualification...  ...overseeing Computer System Validation (CSV) activities including URS FS RA IQ OQ PQ...  .... Educational background in Science Engineering or IT with 5 years pharmaceutical or... 

 ...Designation/Service provider QA Validation Specialist Reporting to whom...  ...and procedures. Support to production / engineering to ensure the qualified state of equipment...  ...advice for qualification activities including CSV qualification and data integrity. Provide... 

 ...dynamic and fast-paced environment. R&D Partners is seeking a QA Validation Specialist to support the qualification and validation of...  ...operations. The successful candidate will work cross-functionally with engineering, production, and quality teams to support ongoing and project-... 

 ...Are you looking for a new challenge in engineering? Step into a high-impact role where your expertise in utility validation helps power the future of pharmaceutical innovation. R&D Partners is seeking a QA Validation Engineer - Utilities to join a pharmaceutical company... 

Abbott in Ireland Abbott serves the Irish market with a diverse range of healthcare products, including diagnostics, medical devices, and nutritional products. In Ireland, Abbott employs over 6,000 people across ten sites. We have seven manufacturing facilities located in...

 ...the role We’re looking for a forward-thinking Manufacturing Engineer to join our team and help shape the future of production. This...  ...and suppliers. Ensure Compliance : Participate in validation and quality assurance activities, ensuring all work meets regulatory... 

 ...enthusiastic Graduate or Junior Automation Engineers with exposure to GMP-regulated...  ...Participate in commissioning, qualification, and validation activities (IQ, OQ, PQ) for automated...  ...systems or  platforms. Knowledge of GAMP5, CSV, data integrity, or validation principles... 

 ...Purpose: Boston Scientific Clonmel is hiring a Process Engineer III to join its Process Development Team. This role will work cross...  ...strong knowledge and application of Process and equipment validation techniques (IQ, OQ, PQ), PFMEA’s, and associated regulatory requirements... 

 ...possibilities for a brighter tomorrow We are seeking a Process Engineer II on a permanent basis to join our team. Purpose:...  ...Demonstrates knowledge and application of Process and equipment validation techniques (IQ, OQ, PQ), FMEA, and associated regulatory requirements... 

 ...they relate to technology selection system configuration SDLC validation hardware software environments and business processes. Partner...  ...Knowledge Skills & Education: Required: BS in Engineering Computer Science or other technical degree. Training completed... 

 ...Position: Automation Project Engineer.  Location: Munster, Ireland. PACIV, a global leader in industrial automation solutions with...  ...equipment. Support specification, procurement, implementation, and validation of automated systems, ensuring adherence to GMP procedures on-... 

 ...Position: PLC Automation Engineer.    Location: Munster, Ireland. PACIV, a global leader in industrial automation solutions with offices...  ...manner to provide clarity and a path forward on any issues. ~ Applicants must have a valid EU Work Permit and Irish Residency...