Senior Director-molecule Steward Lead

GSK

Upper Providence, PA, United States
Base: $220,275 to $367,125; bonus/equity: annual b...
Hybrid
End-to-end technical accountability for drug substance and product
Experience with technology transfer activities
Knowledge of fda ema mhra regulatory frameworks
GSK is seeking a Senior Director-Molecule Steward Lead to manage a team responsible for technical leadership in the development and lifecycle management of innovative biopharmaceutical products. This hybrid role requires a strong background in biopharmaceutical development, team leadership, and collaboration across various functions

Job Summary

  • The Senior Director will lead a group of 5-15 Molecule Stewards responsible for the end-to-end technical accountability of innovative pharmaceutical programs including drug substance and product manufacturing.
  • This role requires defining and owning the technical strategy throughout the product lifecycle, including technology transfers, performance qualification, and ongoing continuous process verification.
  • GSK offers a comprehensive benefits program including health care, retirement benefits, paid holidays, and eligibility for share-based long-term incentive programs.

Matching Summary

Match Score: 85

GSK is seeking a Senior Director-Molecule Steward Lead to manage a team responsible for technical leadership in the development and lifecycle management of innovative biopharmaceutical products. This hybrid role requires a strong background in biopharmaceutical development, team leadership, and collaboration across various functions.

Salary

Base: $220,275 to $367,125; Bonus/Equity: Annual bonus and share-based long term incentive program; Benefits: Health care, retirement, paid holidays, vacation, and parental leave

Skills & Requirements

Must-have

  • End-to-end technical accountability for drug substance and product
  • Experience with technology transfer activities
  • Knowledge of FDA EMA MHRA regulatory frameworks
  • Leadership of cross-functional matrixed teams
  • Expertise in Product Control Strategy development

Nice-to-have

  • Strong communication skills for diverse audiences
  • Experience with risk-based project management tools
  • Comfort working in global cross-cultural teams
  • Deep expertise in long-acting injectable products
  • Ability to mentor and develop technical talent

Key Requirements

  • Bachelor's degree in life sciences or related field
  • Experience in biopharmaceutical development
  • Experience supporting molecule program management across preclinical/clinical stages
  • Experience with external regulatory frameworks (FDA, EMA, MHRA)

Work Rights

Not specified

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