Our client, Norgine, is a leading European specialist pharmaceutical company with over 110 years of expertise and a presence in all major European markets. Their vision is to be the „go to“ European specialist pharmacy company, which means that they want to be the organisation that other companies come to in order to develop and commercialise their products in Europe. 

Norgine Alps is one of the Commercial RCUs within the company represented in Austria, Switzerland and Liechtenstein. For their office in Vienna the company is currently looking for a Medical Manager, who manages the Medical Department and Medical Activities and Medical Information in Austria, Switzerland and Liechtenstein.

In this exciting role the position holder leads a team of two Medical employees and is also part of the Alps leadership team.

Your tasks

  • Act as QMR (Quality Management Representative) and local Pharmacovigilance officer. Technical Director (Gewerberechtlicher Geschäftsführer AMBO 2009, §10) and QMR (Quality Management Representative) 
  • For Austria: Act as Technical Director (GewerberechtlicherGeschäftsführer; Befähigung zum Großhandel mit Arzneimittel und Giften), Adept Person ("Fachkundige Person") according to the Austrian Medicinal Products Site Regulation (AMBO 2009, §10) and person designated responsible for information (“Information Officer”) according to the Medicinal Products Act Austria (AMG 2013, § 56) as well as local contact person for Pharmacovigilance
  • For Switzerland: Procuration (joint authorization)
  • Develop and ensure that all promotional materials together with Sales and Marketing activities is made according to applicable WPs and SOPs, medicine legislation and applicable codes of practice
  • Coordinating marketing activities
  • Reporting and Budgeting of Medical activities
  • Participate in cross-functional projects and meetings as a representative of the medical function
  • Train sales force on product background and pharmacovigilance
  • Responsible for interactions with key opinion leaders and management of investigator initiative studies

Your qualifications

  • Life science degree (Dr. med.) with at least 4 years of pharmaceutical experience
  • Excellent training and experience in copy approval incl. all aspects of legislation and relevant codes of practice regulation the promotion of medicines in AT and CH
  • Working knowledge of drug safety regulations 
  • Strong leadership and excellent communications skills
  • Clinical understanding on therapeutic areas
  • Influencing skills
  • Ability to work effectively as part of a successful and highly motivated Leadership team
  • Proactive approach to working in sales and marketing environment
  • Organizational skills to manage day to day business effectively including having good IT skills
  • Being able to understand and speak English and German 
  • Be problem solving and have analytical skills
  • Solution oriented focus and handle stress well

Remuneration: EUR 80.000 gross annual salary (excl. variable pay) with willingness to overpay

If you are interested in this challenging position, please forward your CV and a recent photograph quoting reference number E9018 to