Senior Principal Scientist, Large Molecule Drug Product Scientific Integrator

Johnson & Johnson

Malvern, Pennsylvania, United States
**
Large molecule drug product development
Late-stage program integration
Global cmc team representation
** Johnson & Johnson is seeking a Senior Principal Scientist for its Large Molecule Drug Product Scientific Integrator role in Malvern, PA. The position involves leading late-stage drug product development programs and requires extensive experience in biopharmaceuticals, particularly in regulatory strategy and cross-functional collaboration. **

Job Summary

  • This role provides single‑point accountability for Drug Product strategy within the global Chemistry, Manufacturing, and Control (CMC) team(s), ensuring alignment across formulation, process, delivery system, analytical, manufacturing, quality, regulatory, and supply chain functions.
  • The Scientific Integrator plays a critical role in right‑first‑time registration, launch readiness, and lifecycle success, acting as a trusted scientific advisor and matrix leader across global teams.
  • We provide an inclusive work environment where each person is considered as an individual.

Matching Summary

Match Score: 75

** Johnson & Johnson is seeking a Senior Principal Scientist for its Large Molecule Drug Product Scientific Integrator role in Malvern, PA. The position involves leading late-stage drug product development programs and requires extensive experience in biopharmaceuticals, particularly in regulatory strategy and cross-functional collaboration. **

Skills & Requirements

Must-have

  • Large Molecule Drug Product Development
  • Late-stage program integration
  • Global CMC team representation
  • Drug Product strategy ownership
  • Regulatory submission authoring

Nice-to-have

  • Mentoring and coaching scientists
  • Cross-functional matrix leadership
  • Health Authority interaction experience
  • Complex delivery systems familiarity

Key Requirements

  • PhD with 6+ years of experience
  • Master's degree with 10+ years of experience
  • Late-stage registration/commercial program experience
  • Parenteral biologics CMC strategy experience
  • Regulatory submission authoring/review experience

Work Rights

Not specified

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