Senior/Team Lead International Regulatory Affairs

Your responsibility

  • Overall responsibility for all approval processes (incl. life cycle management) in approx. 35 countries worldwide
  • Management and further development of the 12-strong team
  • Developing the approval strategy for the region, including meeting deadlines through targeted prioritization
  • Main contact person for Business Development and Market Access in order to achieve overarching goals and make decisions
  • Close coordination with authorities, including occasional on-site presence
  • Close interface coordination as part of the approval process

Dein Hintergrund

  • Successfully completed scientific studies
  • Relevant experience in international marketing authorization of medicinal products
  • Initial management experience desirable – but can also be developed on site
  • Strong analytical and forward thinking skills
  • Fluency in English
  • Good knowledge of German
  • Ideally good knowledge of French
  • Willingness to travel globally (approx. once a month)

Deine Benefits

  • A wide range of development opportunities
  • Employee benefits, such as fitness allowances and much more
  • Regular team events and numerous company celebrations
  • Firmly anchored and „lived“ corporate culture
  • 40% mobile working
  • 30 days vacation per year
Gender note

For reasons of better readability the language forms masculine, feminine and diverse (m/f/*) are used simultaneously. All references to persons apply equally to all genders.

Type of contract

Permanent Position

Industry

Pharmaceuticals

Department

Regulatory Affairs

Location

Munich

Germany

Entry date

ASAP

Duration

Permanent

Remote

teilweise

Capacity (FTE)

1

Dein Ansprechpartner
DST
Danijela Stevanovic

Senior Recruiting Managerin

DST
Danijela Stevanovic

Senior Recruiting Managerin

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