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FRFresenius Kabi SwissBioSim GmbH

Senior Manager Regulatory Affairs Lead(m/w/x)

Eysins
VollzeitVor OrtSenior

Global regulatory leadership for biosimilar development, managing submission dossiers and health authority meeting preparations. 6-8 years international regulatory experience with global submission (US BLA/EU MAA) required. Global project scope, international team collaboration.

Anforderungen

  • Degree in life science or related disciplines
  • At least 6-8 years in international regulatory
  • Experience in managing international or regional regulatory submissions, normally a full global submission (new product application), preferably US BLA or EU MAA
  • Experience in working in development project teams
  • Experience in leading regulatory agency interactions including management of the associated documentation and rehearsals
  • Experience in preparation and coordination of regulatory strategy plan
  • Experience in biological development
  • Experience in CTA requirements
  • Capability to manage a number and range of projects throughout development
  • Excellent written and spoken communication skills
  • Excellent interpersonal skills
  • Understanding of Regulatory Affairs contribution to Pharma business
  • Excellent organizational skills, work independently, self-motivated and proactive
  • Attention to details, without losing the overall picture
  • Ability to think strategically
  • Ability to lead regulatory sub team and work in teams
  • Autonomous, goal-oriented and pragmatic
  • Strong customer-orientation and strong communication skills
  • Fluent command of spoken and written English, additional language skills welcome

Aufgaben

  • Provide global regulatory leadership for biosimilar development
  • Manage submission-related documents and regulatory data for biosimilars
  • Lead preparation and rehearsal for meetings with Health Authorities
  • Develop and manage the submission strategy for biosimilar dossiers
  • Ensure compliance with Fresenius Kabi regulatory procedures
  • Establish regulatory storylines for interactions with authorities
  • Collaborate with Regulatory Operations to implement technology strategies
  • Support market units in interactions with local health authorities
  • Contribute to wave 2 submission prioritization assessments
  • Guide Launch Readiness Plans with regulatory process insights
  • Lead the Regulatory Sub-team and Strategic Submission Teams as needed
  • Act as Regional Lead for US, Canada, or EU regulatory responsibilities
  • Manage the regulatory submission process through to approval
  • Coordinate regulatory agency interactions and document preparation
  • Provide recommendations on submission readiness
  • Stay updated on the current regulatory environment
  • Interface with other regulatory groups and company functions
  • Perform additional tasks to support regulatory objectives
  • Drive collaboration with third-party partners for regulatory tasks
  • Mentor Junior Regulatory Affairs Leaders

Berufserfahrung

  • 6 - 8 Jahre

Ausbildung

  • Bachelor-Abschluss

Sprachen

  • Englischverhandlungssicher
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