Lead, Oral Drug Product Projects - Late-Phase Development

C028 (FCRS = CH028) Novartis Pharma AG

Basel

Sur place

CHF 94 000 - 174 000

Plein temps

Il y a 10 jours

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Avantages offerts par ce poste

Insurance plans
Retirement plans
Wellbeing resources
Global recognition programs
Flexible and hybrid working options
14 weeks parental leave

Résumé du poste

Novartis Pharma AG in Basel, Switzerland is seeking a Drug Product Project Leader (DPPL) to drive late-phase oral drug product development. You will lead DP development strategies, manage budgets and timelines, and coach high-performing cross-functional teams to deliver compliant CMC documentation.

You will collaborate with global development teams, apply quality-by-design principles, assess risks, and ensure alignment with internal functions and external partners.

Qualifications

  • Advanced Degree in Pharmaceutical Technology, Powder Process Engineering, or related field.
  • Minimum 5+ years of industry experience in development of pharmaceutical formulations.
  • Strong understanding of Quality by Design (QbD) and regulatory guidelines.
  • Experience leading cross-functional teams in GMP/GLP environments.
  • Excellent leadership, scientific, and project management and presentation skills.

Responsabilités

  • Represent DP project teams, providing quality awareness and technical leadership.
  • Develop robust DP project strategies, including risk assessments and budgets.
  • Consolidate resources and lead budgeting for DP activities.
  • Ensure adherence to governance processes and DP strategies within the team.
  • Oversee cross-functional interactions, track plans, and deliver DP documentation for CMC submissions.
  • Understand how formulation design and process parameters influence product performance.

Connaissances

Leadership
Project management
Communication
Cross-functional collaboration
Strategic thinking

Formation

PhD or equivalent

Description du poste

Novartis Pharma AG in Basel, Switzerland is seeking a Drug Product Project Leader (DPPL) to drive late-phase oral drug product development. You will lead DP development strategies, manage budgets and timelines, and coach high-performing cross-functional teams to deliver compliant CMC documentation.

You will collaborate with global development teams, apply quality-by-design principles, assess risks, and ensure alignment with internal functions and external partners.

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