Senior Director-molecule Steward Lead

GlaxoSmithKline

Upper Providence, PA, United States
Base: $220,275 to $367,125; bonus/equity: annual b...
**
End-to-end technical accountability for drug substance and product
Experience with technology transfer activities
Knowledge of fda ema mhra regulatory frameworks
** GlaxoSmithKline is seeking a Senior Director-Molecule Steward Lead to oversee a team of Molecule Stewards responsible for the technical leadership of drug products and ensuring successful product lifecycle management. The role requires expertise in biopharmaceutical development and strong communication skills, with a focus on managing cross-functional teams and stakeholders. **

Job Summary

  • The Senior Director will lead a team of 5-15 Molecule Stewards responsible for the end-to-end technical lifecycle of innovative pharmaceutical programs from development through commercial launch.
  • This role requires defining and owning the technical strategy for long-acting injectable products, ensuring alignment across global supply nodes and maintaining strict quality and robustness standards.
  • GSK offers a competitive compensation package including an annual bonus, share-based long-term incentives, and comprehensive health and retirement benefits for eligible employees.

Matching Summary

Match Score: 75

** GlaxoSmithKline is seeking a Senior Director-Molecule Steward Lead to oversee a team of Molecule Stewards responsible for the technical leadership of drug products and ensuring successful product lifecycle management. The role requires expertise in biopharmaceutical development and strong communication skills, with a focus on managing cross-functional teams and stakeholders. **

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 development teams
  • Expertise in Product Control Strategy development

Nice-to-have

  • Strong communication skills presenting to diverse audiences
  • Experience using risk-based approaches and project tools
  • Comfort working in cross-cultural global teams
  • Deep technical expertise in long-acting injectables
  • Mentoring capabilities for technical talent development

Key Requirements

  • Bachelor's degree in life sciences or related field
  • Experience in biopharmaceutical development and molecule program management
  • Proven track record supporting technology transfer in clinical stages

Work Rights

Not specified

Tailored Resume

Cover Letter