Drug Safety Specialist

We are seeking aDrug Safety Specialistwith35 years of pharmacovigilance experienceand a clinical background (RN, BSN, RPh, or PharmD). The ideal candidate will support end-to-end adverse event case processing for marketed and investigational products, ensuring compliance with FDA, ICH, and Google Cloud Platform regulations. Required Skills: 35 years of Drug Safety/Pharmacovigilance experienceClinical degree (RN, BSN, RPh, or PharmD)Experience with AE/SAE case processing and safety surveillanceKn

Job#: 3043177 Job Description: Contractor, Safety Systems (Pharmacovigilance) Our biotech client is seeking an experienced Contractor, Safety Systems to support the administration, maintenance, and optimization of global pharmacovigilance (PV) safety systems. This individual will serve as a subject matter expert for safety databases and reporting tools, ensuring compliance, system integrity, and operational efficiency across global safety operations. Key Responsibilities Administer and maintai

By clicking the ?Apply? button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda?s and . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as Associate Director, Quantitative Clin

Job Summary: We are seeking a Computer System Validation (CSV) Engineer with experience in Computer System Validation (CSV) within a GMP-regulated pharmaceutical or biotechnology environment. The ideal candidate will have expertise in GAMP 5, 21 CFR Part 11, validation lifecycle documentation, and QC laboratory or manufacturing systems validation, while collaborating with cross-functional teams to ensure regulatory compliance. Roles & Responsibilities: Develop, execute, and maintain Computer S