ratiotx

ratiotx

Validation Engineer

West Valley City, Utah

Sponsorship not specifiedDetected 20 days ago
GMPResearchCommunicationOrganizational Skills

About the role

  • About Ratio Therapeutics Ratio Therapeutics is committed to improving and extending the lives of cancer patients without sacrificing their quality of life.
  • Join us in our quest to become the leading innovator in radioligand therapy and improve the lives of cancer patients and their families.

Responsibilities

  • Perform commissioning, qualification, and validation activities in alignment with project schedules and site procedures
  • Create, review, and revise qualification-related documents, including SOPs, validation plans, master plans, and execution plans
  • Lead or support design reviews, factory acceptance testing (FAT), commissioning, and qualification activities
  • Lead periodic review activities for validated systems and equipment
  • Partner cross-functionally with internal departments, and external vendors to ensure compliant execution of CQV activities
  • Lead small to mid-sized capital projects and provide validation support for larger projects

Requirements

  • Bachelor's degree in Engineering or a related technical field
  • 5+ years of relevant validation or qualification experience in a GMP-regulated environment
  • Hands-on experience with equipment, utility, or facility qualification and lifecycle validation practices
  • Familiarity with risk-based validation principles and good documentation practices
  • Ability to work safely in a manufacturing environment
  • Strong communication skills with the ability to clearly summarize technical topics for cross-functional audiences
  • The ideal candidate will enjoy working in a collaborative, fast-paced, multidisciplinary environment.

Nice to have

  • Experience with digital validation platforms such as ValKit or Kneat
  • Experience supporting commissioning and qualification during facility startup or expansion
  • Knowledge of aseptic manufacturing environments strongly preferred
  • Experience in radiopharmaceutical, pharmaceutical, biotech, or other highly regulated manufacturing operations
  • Experience supporting change control, deviations, and validation impact assessments

Compensation

  • The annual base salary for this role is expected to range between $90,000 and $120,000.

This listing is sourced directly from ratiotx's careers page and normalized into a canonical job model.