Veeda Lifesciences is seeking a passionate “Pharmacovigilance QA”.
Job Location : Ahmedabad
Experience Required: 1 to 2 Years
Education Required: B pharma and M pharma
Responsibilities:
To prepare audit plan, audit report, compliance verification, corrective and preventative actions (CAPA) closure of
Study based audits for clinical studies (including Phase-1 and BA/BE studies) as per audit plan in compliance with ICH-GCP, Indian GCP, internal procedures (SOP), protocol and applicable regulatory requirements
Clinical studies audit and releasing audit certificate
In-process audits of IMP related activities like dispensing, retention etc.
Veeda Lifesciences is an internationally recognized contract research organization (CRO) that delivers a wide range of services—including clinical, preclinical, and bioanalytical solutions—to advance the development of generic, biosimilar, and innovative drugs.
Operating across several global locations, Veeda offers specialized support in preclinical research, bioavailability/bioequivalence (BA/BE) studies, bioanalytical testing, and clinical trials spanning all phases (Phase I to Phase IV).
Known for its scientific rigor, adherence to regulatory standards, and commitment to ethical conduct, Veeda upholds the highest research quality by continually investing in skilled professionals, robust processes, and cutting-edge technologies.
