Regulatory Affairs Project Manager (m/w/d)

Location: 

Vienna, AT, 1030 Herrenberg, DE, 71083

Description Overview

Perrigo Company is dedicated to making lives better by bringing high quality and affordable self-care products that consumers trust everywhere they are sold.  Help us do it. We are looking for the following:

Regulatory Affairs Project Manager DACH (m/w/d)

Based in Stuttgart, Vienna or Remote

Reporting Line: Senior Regulatory Affairs Manager DACH

Scope of the Role

  • Ensuring regulatory compliance for an interesting and diverse OTC and Self-Care portfolio
  • Regulatory responsibility across several product classifications, such as OTC medicines, medical devices, food (food supplements, meal replacements, FSMP), cosmetics and consumer goods
  • Planning and handling of regulatory life-cycle activities with a focus on OTC medicines
  • Provide mandatory labelling elements
  • Approval of promotional material and labelling
  • Responsibility as Drug Information Officer in Germany and Austria
  • Provide scientific support for our well-known brands
  • Support Consumer Service team with responses to customer and consumer enquiries
  • Monitoring and interpretation of applicable legislation and requirements for the various product categories
  • Communication with authorities and associations within the Regulatory Affairs network across DACH
  • Close cooperation with local Patient Safety, Quality, Marketing and Sales teams and with the Central functions in our business unit Consumer Self-Care International
  • Active support of DACH teams and international project teams, e.g. regarding new product launches and product changes
  • Lead regulatory projects
  • Active contribution to the constant improvement of processes and their implementation in the recently established DACH cluster organisation

Experience Required

  • Master degree in natural sciences, preferably pharmacy, chemistry, biology or similar degree
  • Several years of professional experience in Regulatory Affairs, ideally in an OTC environment
  • Experience in Drug Advertising and qualification as Drug Information Officer Germany and/or Austria preferable
  • Profound knowledge of the regulatory environment on national (Austria, Germany, Switzerland) and EU level
  • Languages: fluent in German and English (both written and spoken),
  • Proficiency in Microsoft Office applications
  • Strong team spirit, communication skills
  • Reliability, engagement, pro-active mindset, innovative and analytical thinking
  • Outcome-oriented, precise and independent way of working
  • Customer and consumer oriented mindset