Senior Qa Csv Auditor For Fda-ready Di

Purpose Provide independent quality oversight and documented challenge of OT CSV and data-integrity remediation. Revised responsibilities Review/challenge scope, risk rankings, test strategy, deviations, validation reports and CAPA evidence. Verify independence from authors/executors and identify unresolved GMP risks. Review DI controls and critical...

Provide independent quality oversight and documented challenge of OT CSV and data-integrity remediation.PurposeProvide independent quality oversight and documented challenge of OT CSV and data-integrity remediation.Revised responsibilitiesReview/challenge scope, risk rankings, test strategy, deviations, validation reports and CAPA evidence.Verify...

Location Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. The site in Visp, Switzerland is growing and for our Biologics Quality organization, we are currently looking for a Senior QA Specialist (f/m/d) for the Bioconjugates plant. What you will get An...

Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.The site in Visp, Switzerland is growing and for our Biologics Quality organization, we are currently looking for a Senior QA Specialist (f/m/d) for the Bioconjugates plant. The successful candidate will...

Senior Scientist QC BioanalyticsLonzaVisp, SwitzerlandAt the Visp site, we are looking for a Scientist (m/f/d). As a member of our great Quality Control team, you will be responsible for the routine execution of various biochemical methods, focusing on ELISA, qPCR, ProA and enzyme assays, while adhering to GMP and safety guidelines.Key...

About Usten23 health is a human-centric and sustainable strategic partner of choice for the pharmaceutical industry and biotech start-ups for the development, manufacture, and testing of tomorrow's medicines. We support our clients in developing differentiated, stable, usable, and safe injectable treatments for patients. Your mission We are looking for a...

SGI is seeking an experienced QA/CSV professional to provide independent GMP QA oversight of computerized systems and prepare inspection narratives. The role requires direct FDA inspection exposure, strong knowledge of Part 11, Annex 11, and DI guidance, with DeltaV familiarity and travel to Visp (2 days/month).The successful candidate will challenge risk...

Source Group International seeks a senior QA professional to provide independent oversight of GMP CSV activities and data integrity remediation. The role requires navigating regulatory expectations, supervising CAPA evidence, and ensuring inspection readiness for FDA-related reviews.The ideal candidate has extensive QA experience in computerized systems,...

PurposeProvide independent quality oversight and documented challenge of OT CSV and data-integrity remediation.Revised responsibilitiesReview/challenge scope, risk rankings, test strategy, deviations, validation reports and CAPA evidence.Verify independence from authors/executors and identify unresolved GMP risks.Review DI controls and critical...