Sauvegarder Retour à la recherche Description du poste Résumé Offres similaires Mise à jour le 20/10/2026Fast growing Biotech companyBiologics Licence Application Program ManagementÀ propos de notre clientWe are mandated by our client, an innovative biotech company based in Lausanne.Description du posteBLA Program Management- Build, own and continuously maintain the integrated BLA master plan from pre-BLA meeting preparation through submission, filing, review, potential inspections, labeling negotiations and post-action commitments with external BLA regulatory consultants and dossier delivery team.- Ensure all five CTD module plans are appropriately planned and integrated, including US regional content, summaries/overviews, CMC, nonclinical, clinical and labeling. Maintain the respective authoring, review, approval and publishing calendar as part of the overall BLA master plan.Cross-functional Governance and Execution- Establish and run the BLA Team, including meeting cadence, agendas, decision records and action logs.- Prepare concise program updates for the CEO and Executive Committee, Board, and investors as appropriate.Health Authority Meeting, inspection & response Readiness- Establish and run the BLA Team, including meeting cadence, agendas, decision records and action logs.- Prepare concise program updates for the CEO and Executive Committee, Board, and investors as appropriate.- Coordinate operational preparation for Health Authority meetings, including briefing-book timelines, internal alignment, rehearsal, follow-up actions and agency-commitment tracking.- Coordinate FDA pre-approval inspection readiness across internal teams, CMO, analytical laboratories, CROs and clinical sites.- Establish and maintain the review "war room" for rapid, high-quality responses to FDA information requests.Profil recherchéThe ideal candidate combines profound project management capabilities with hands-on leadership without authority skills and BLA delivery experience to deliver the right BLA-ready content, decisions, evidence, quality checks and inspection-readiness activities on time.Experience- Proven track record of successfully coordinating cross-functional teams and external CRO/CDMO/vendor networks in a small or mid-sized biotech environment.- Structured, decisive and hands-on. Turns a complex biologics submission into a clear, accountable plan without creating unnecessary process.- Proven ability to lead complex cross-functional teams without authority. Collaborative but firm. Protecting functional ownership while ensuring program-level decisions and timelines are me- Executive ready communicator. Provides concise, decision-oriented reporting to the Executive Committee, Board and external partners.Qualifications- 10+ years in biotech/pharma program management, development operations, regulatory project management, or submission management- BLA delivery experience from pre-submission through review and approval is strongly preferred.- Strong familiarity with CTD design and submissions, FDA meeting preparation, information-request management, and inspection readiness a plus- Strong Project Management skills- Excellent written and spoken English required.Informations complémentairesPermanent positionIndiquer la référence de l'offreJN-102026-7128432Résumé du posteSecteurSanté & Sciences de la VieSpécialisationBiotechnologie IndustrieHealthcare / PharmaceuticalOù ?LausanneType de contratPermanentRéférence de l´offreJN-102026-7128432
