Director, Rayzebio Quality Systems And Compliance

RayzeBio

Indianapolis, IN, USA
Base: $190,989 - $231,434; bonus/equity: + incenti...
Fully remote
Quality management system (qms) implementation
Gxp electronic systems implementation
Regulatory inspection readiness
The Director, RayzeBio Quality Systems and Compliance is responsible for providing leadership and expertise in creating, implementing, and communicating the execution and effectiveness of the Quality Management System (QMS) at RayzeBio

Job Summary

  • The Director, RayzeBio Quality Systems and Compliance is responsible for providing leadership and expertise in creating, implementing, and communicating the execution and effectiveness of the Quality Management System (QMS) at RayzeBio.
  • This role influences leadership on the strategic direction and tactical implementation of the quality systems for radiopharmaceutical operations and establishes QMS specific quality objectives, priorities, and roadmap.
  • Benefits include health coverage, wellbeing support, financial well-being and protection, and work-life benefits such as flexible time off and paid holidays.

Matching Summary

The Director, RayzeBio Quality Systems and Compliance is responsible for providing leadership and expertise in creating, implementing, and communicating the execution and effectiveness of the Quality Management System (QMS) at RayzeBio.

Salary

Base: $190,989 - $231,434; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Health Coverage, Wellbeing Support, Financial Well-being and Protection, Work-life benefits

Skills & Requirements

Must-have

  • Quality Management System (QMS) implementation
  • GxP electronic systems implementation
  • Regulatory inspection readiness
  • Supplier qualification program
  • Data Integrity initiatives

Nice-to-have

  • Transformative radiopharmaceutical therapies
  • Nimble, pioneering spirit
  • Multidisciplinary team collaboration
  • Continuous quality improvement
  • QA release by exception vision

Key Requirements

  • Bachelor’s degree in science, engineering, or pharmaceutical-related discipline
  • 10+ years of pharmaceutical quality leadership experience
  • Previous experience in implementing and developing quality systems
  • Previous experience in directly dealing with GMP health authority inspections
  • Prior regulatory inspection readiness and inspection execution experience
  • Strong knowledge of cGMP regulations

Work Rights

Not specified

Tailored Resume

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