Amina Hanif

I am a pharmaceutical scientist with three years' experience in GMP-regulated environments and a First Class BSc in Pharmaceutical Science. I combine hands-on analytical testing with a strong foundation in regulatory compliance and data integrity.

At PSS Eurofins I conduct stability testing in line with ICH Q1A(R2) and maintain audit-ready documentation in Veeva Vault, Sample Manager and ELNs, applying ALCOA principles. I investigate deviations, perform root cause analysis, and support expiry verification and packaging compliance.

Previously at Viatris I performed HPLC/UPLC testing, NGI and APSD analysis and supported method development using ICH Q2(R2) and Q8(R2). I resolved anomalous results, maintained GxP-compliant records in Documentum and collaborated with formulation and material science teams to ensure accurate, compliant reporting.

I am expanding my pharmacovigilance expertise through self-study of ICH E2A, GVP Modules and MHRA guidance and am eager to transfer my quality and regulatory skills into PV case processing. I seek roles where my analytical rigour, audit readiness and documentation practices can strengthen patient-safety focused processes.