Specialist - Analytical
• Responsible for planning stability studies, writing and/or review of stability protocols, reports, and preparation of technical documents in CTD format. • Co-ordinate and follow up stability studies at contract research organisations (CROs)/ Chemical Quality Control lab of Orion (CQC). • Co-ordinate and follow up validation and method transfer at CROs. • Write/check/review analytical and pharmaceutical documents as per regulatory requirements (method and validation...