Senior Manager, Msat

Moderna

Norwood, US
Base: $130,800.00 - $209,400.00; bonus/equity: eli...
70% in-office, 30% remote
Cgmp manufacturing experience
Drug product technical transfer
Process validation
Moderna is seeking a Senior Manager for its MSAT team in Norwood, US, to lead the technical transfer and process validation of mRNA-based drug products. The ideal candidate will have extensive experience in the pharmaceutical/biotechnology industry, focusing on cGMP manufacturing and process optimization

Job Summary

  • Serve as a central figure in ensuring the successful transfer and validation of mRNA-based drug product manufacturing processes.
  • Lead the execution of Technical Transfer and Process Validation activities, including protocol creation, PPQ execution, and report generation.
  • Support the global expansion of Moderna’s manufacturing network and provide close exposure to cutting-edge digital and AI-based tools.

Matching Summary

Match Score: 85

Moderna is seeking a Senior Manager for its MSAT team in Norwood, US, to lead the technical transfer and process validation of mRNA-based drug products. The ideal candidate will have extensive experience in the pharmaceutical/biotechnology industry, focusing on cGMP manufacturing and process optimization.

Salary

Base: $130,800.00 - $209,400.00; Bonus/Equity: Eligible for annual discretionary bonus, other incentive compensation, or equity award; Benefits: Best-in-class healthcare, holistic well-being support, family planning benefits, generous PTO, savings and investment opportunities

Skills & Requirements

Must-have

  • cGMP manufacturing experience
  • drug product technical transfer
  • process validation
  • cross-functional collaboration
  • regulatory submissions support

Nice-to-have

  • digital tools and AI integration
  • continuous improvement methodologies
  • risk assessment facilitation
  • culture of safety and innovation

Key Requirements

  • 10+ years in pharmaceutical/biotechnology industry
  • Science Degree with pharmaceutical/biotechnology applicability
  • Knowledge of drug product manufacturing

Work Rights

Must be a US person (citizen, permanent resident, asylee, or refugee)

Tailored Resume

Cover Letter