Dominic Jud

Regulatory Affairs Professional in the Biopharm department at headquarters of Novo Nordisk in Copenhagen. Including early stage clinical development and LCM activities.

Teaching assignment at the Swiss Federal Institute of Technology (ETH) in Zurich for the Module Regulatory Affairs in the Master's curriculum Pharmaceutical Sciences.

Regulatory Affairs Manager in the Swiss Affiliate of Novo Nordisk.

6 month internship at Novartis TRD-Biologics, Late Phase Analytical and Pharmaceutical Development group

Pharmacist (20 %) with the following responsibilities: - Head of the analytical laboratory - Risk assessment of chemical/physical identification reactions (Ph. Eur.) - Process development of analytical testing according to national regulations - Implementation of analytical tests in the laboratory - Setting up of a MS Access database, writing protocols and standard operation procedures and working in a quality management system (QMS)

Sales and field agent in sales promotion, customer advice and product sampling for different companies and brands of the electronic, food, cosmetic, and telecommunication sectors.

Project Management Module according to IPMA Competence Baseline: Contextual / Technical / Behavioural Competences Advanced Project Management Module: Project management systems (PMS) / Projects in an international environment / Agile methods / Project portfolio management