Senior Manager, Master Production Planning – Clinical Supply

Gilead Sciences

Bay Area, CA, US
Base: $157,590.00 - $203,940.00 (bay area); $143,2...
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8 years experience in production planning
Master production schedule ownership
Gmp/gxp compliance knowledge
** Gilead Sciences is seeking a Senior Manager for Master Production Planning in Clinical Supply, responsible for overseeing clinical master production planning strategies. The ideal candidate will possess significant experience in supply planning within a regulated pharmaceutical environment and demonstrate strong leadership qualities. **

Job Summary

  • This role oversees strategy and execution for clinical master production planning across multiple programs to ensure an agile, compliant supply of investigational medicinal products.
  • The position requires balancing trial needs with capacity, inventory, and timelines while managing risk governance and decision support across functions.
  • Employees are eligible for a discretionary annual bonus, stock-based long-term incentives, and a comprehensive benefits package including medical, dental, vision, and life insurance.

Matching Summary

Match Score: 75

** Gilead Sciences is seeking a Senior Manager for Master Production Planning in Clinical Supply, responsible for overseeing clinical master production planning strategies. The ideal candidate will possess significant experience in supply planning within a regulated pharmaceutical environment and demonstrate strong leadership qualities. **

Salary

Base: $157,590.00 - $203,940.00 (Bay Area); $143,225.00 - $185,350.00 (Other US); Bonus/Equity: Discretionary annual bonus and stock-based incentives; Benefits: Medical, dental, vision, life insurance

Skills & Requirements

Must-have

  • 8 years experience in production planning
  • Master Production Schedule ownership
  • GMP/GxP compliance knowledge
  • Clinical trial supply management
  • Cross-functional leadership skills

Nice-to-have

  • Experience with IVRS and ERP systems
  • Project management certification
  • Strategic enterprise thinking
  • Digital transformation sponsorship
  • Strong written communication skills

Key Requirements

  • Bachelor's Degree with 8 years experience OR Master's with 6 years
  • PhD/PharmD with 2 years experience
  • Knowledge of Phase I-III clinical study designs
  • Experience leading complex high-uncertainty supply portfolios

Work Rights

Not specified

Tailored Resume

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