Drug Product Project Leader (m/f/d) – Associate Director Science & Technology

Novartis

Schaftenau, Austria
Base: €78,383.90 pyear; bonus/equity: attractive i...
Hybrid
Lead technical development strategy for complex biologics
Champion scientific excellence in drug product formulation
Lead and coordinate global drug product sub-team
Novartis is seeking a Drug Product Project Leader (Associate Director Science & Technology) in Schaftenau, Austria, to lead the late-stage development of their biologics product pipeline. The ideal candidate should have extensive experience in drug product formulation, regulatory submissions, and strong leadership abilities

Job Summary

  • Join our global team of highly skilled Drug Product Project Leaders with presence in all technical research and development sites for Biologics at Novartis!
  • As Drug Product Project Leader in Austria, you will be the strategic lead of drug product development of Biologics and be accountable for agreed upon deliverables to the CMC team.
  • In addition to a market-competitive base salary, we offer an attractive incentive program, a modern company pension scheme, childcare facilities, learning and development opportunities as well as worldwide career possibilities within the Novartis group.

Matching Summary

Match Score: 85

Novartis is seeking a Drug Product Project Leader (Associate Director Science & Technology) in Schaftenau, Austria, to lead the late-stage development of their biologics product pipeline. The ideal candidate should have extensive experience in drug product formulation, regulatory submissions, and strong leadership abilities.

Salary

Base: €78,383.90 /year; Bonus/Equity: attractive incentive program; Benefits: modern company pension scheme, childcare facilities, learning and development opportunities

Skills & Requirements

Must-have

  • Lead technical development strategy for complex biologics
  • Champion scientific excellence in drug product formulation
  • Lead and coordinate global drug product sub-team
  • Accountable for timely delivery of high quality source documents
  • Proactively communicate project strategy and requirements
  • Assess and consolidate resource and project budget needs

Nice-to-have

  • Openness to digital transformation
  • Proactiveness in adopting new digital tools
  • Thrive in collaborative, cross-functional environments

Key Requirements

  • Ph.D. in pharmaceutical technology, biotechnology, chemical engineering or equivalent
  • Minimum of 8 years of relevant industry experience
  • Proficient in quality principles, QbD, GMP and regulatory requirements
  • Experience in IND / BLA submissions
  • Excellent leadership and interdisciplinary skills
  • Excellent project management, communication / presentation skills
  • Strategic mindset with strong business acumen
  • Fluency in English (oral and written)

Work Rights

Not specified

Tailored Resume

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