Analytical Expert (Associate Director, Science & Technology)

Role Responsibilities:

•With your strong expertise in analytical development, you take a leading role in supporting analytical control strategies and standards for externalized Drug Substance manufacturing activities (incl. starting materials, intermediates, in-process-control)

• Further, you will support coordination of cGMP related activities at our partners to ensure externalized manufacture under cGMP in a timely and straight forward manner

• As a core member of a cross-functional team, you collaborate closely with our internal and external partners to ensure delivery of new drugs to our patients

• Further, you will support and guide external partners providing relevant process documentation in support of dossier filing

• In this role you also actively participate in scientific exchange groups within Novartis as well as maintaining excellent collaborations with our customers and external partners

What you’ll bring to the team:

• Scientific curiosity coupled with recognized achievements in the development of analytical methods using advanced detection technologies (e.g. UHPLC, GC, SFC and related hyphenated techniques including high resolution MS)

• Dedicated, thoughtful and flexible team working skills

• Strong communication and presentation skills allowing guidance in a scientific sound and compliant way of working towards analytical chemistry teams at external partners

• Good knowledge of English (oral and written) is required, good command of German (spoken/ written) is desirable

• Excellent knowledge of laboratory and/or technical tools

• Good knowledge of analytical software and computer tools such as Office package

Desirable Requirements:

• We are looking for candidates with PhD in analytical chemistry

• Documented and relevant hands-on experience in characterization and release activities for starting materials, intermediates etc. related to small molecule Drug Substances

• A minimum of 3-5 years relevant professional experience in field of analytical development with a strong GMP background is required, preferably in drug substance development

Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Accessibility and accommodation
Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message.