Layla Bagagi

Background

About Layla Bagagi

I am an expert in Pharmaceutical Manufacturing Quality Control & Continuous Improvement with experience overseeing the Physical-Chemical Quality Control Laboratory for pharmaceutical industry leaders such as Bayer, Elanco, Zoetis (Pfizer), Novartis, Syngenta, BASF, Virbac and Boehringer Ingelheim. My background lies in ensuring raw material, and produced goods comply with quality specifications and follow regulations, performing automated and manual methods of quality control and laboratory analysis while supporting all company's lab operations focussing on quality issues. BSc in Chemistry Diploma in Drug Degradation Achievements of my career include: • Led internal audits and ongoing reviews of manufacturing operations and the site's quality systems to ensure they comply with GMP and other internal and external regulations. • Provided QA support to data integrity compliance activities across the site. • Supported Regulatory Inspections and third-party audits and maintained validation documentation. • Ensured laboratory compliance with GMP, United States Pharmacopeia (USP), US Food and Drug Administration (FDA), Data Integrity and Good Documentation Practice (GDP). • Reviewed and monitored analytical data from release and stability testing, reference standard qualification and analytical method validation, reporting results and deviations, and reviewing related data. 083 050 8173 laylabagagi@hotmail.com