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Program Management Director - Biologics Licence Application (BLA)

Michael Page · Lausanne

Nouveau
Senior 🇬🇧 English
Regulatory project management

Description du poste

About the role

A fast-growing biotech company based in Lausanne is looking for a Program Management Director to build, own and maintain its integrated BLA master plan, from pre-submission preparation through submission, filing, review, potential inspections, labeling negotiations and post-action commitments. The role works closely with external BLA regulatory consultants and the dossier delivery team.

Key responsibilities

  • Build and maintain the integrated BLA master plan, covering the five CTD modules (US regional content, summaries, CMC, nonclinical, clinical and labeling)
  • Maintain the authoring, review, approval and publishing calendar as part of the BLA master plan
  • Establish and run the BLA team, including meeting cadence, agendas, decision records and action logs
  • Prepare concise program updates for the CEO, Executive Committee, Board and investors
  • Coordinate operational preparation for Health Authority meetings, including briefing-book timelines, internal alignment, rehearsal and follow-up
  • Coordinate FDA pre-approval inspection readiness across internal teams, CMO, analytical laboratories, CROs and clinical sites
  • Run a review war room for rapid, high-quality responses to FDA information requests

Required profile

  • 10+ years in biotech/pharma program management, development operations, regulatory project management or submission management
  • Proven track record coordinating cross-functional teams and external CRO/CDMO/vendor networks in a small or mid-sized biotech environment
  • Experience leading complex cross-functional teams without authority; collaborative but firm
  • Executive-ready communicator who reports concisely to the Executive Committee, Board and external partners
  • Excellent written and spoken English

Required skills

  • Strong project management skills
  • Familiarity with CTD design and submissions, FDA meeting preparation, information-request management and inspection readiness is a plus

The position is permanent.

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Michael Page

Lausanne