Description

In this role, you will leverage your analytical chemistry expertise to develop strategies for oligonucleotide projects, collaborate with cross-functional teams, and ensure the timely delivery of new therapeutic candidates to patients.

Requirements

• •PhD in analytical chemistry or pharmaceutical analysis
• •Minimum of 3 years of relevant experience in pharmaceutical analysis
• •Scientific curiosity and achievements in developing new analytical methods
• •Strong experience in developing analytical methods using HRMS
• •Dedicated, thoughtful, and flexible teamwork skills
• •Good knowledge of English (oral and written)
• •Good command of German (spoken/written)
• •Excellent knowledge of laboratory and/or technical tools
• •Several years of relevant professional experience in analytical development
• •Good knowledge of software and computer tools such as Office package and analytical software suites

Tasks

• •Establish analytical control strategies for oligonucleotide projects
• •Design and execute experiments in the lab
• •Interpret and report data and results
• •Coordinate cGMP activities for starting materials and intermediates
• •Ensure timely manufacture under GMP within Chemical & Analytical Development
• •Collaborate with internal and external partners to deliver new nucleotide drugs
• •Provide process documentation for dossier filings
• •Participate in scientific exchange groups within Novartis and Academia
• •Maintain collaborations with customers

Tools & Technologies