Associate Director, Quality Management – Translational Medicine Oncology

medizinstellenmarkt.de

Base: $137,344.80 - $206,017.20; bonus/equity: sho...
Quality management system (qms) oversight
Ich-gcp and gxp compliance
Risk-based quality and change control
Join Early Oncology’s Translational Medicine Global Operations team to drive quality across Translational Medicine and Biomarker Science & Technology organizations

Job Summary

  • Join Early Oncology’s Translational Medicine Global Operations team to drive quality across Translational Medicine and Biomarker Science & Technology organizations.
  • The role involves advising on compliance and risk, leading continuous improvement, and championing a culture of quality excellence that delivers high-quality science to patients.
  • A competitive Total Reward program is offered including market driven base salary, bonus, long term incentive, generous paid time off, and comprehensive benefits.

Matching Summary

Join Early Oncology’s Translational Medicine Global Operations team to drive quality across Translational Medicine and Biomarker Science & Technology organizations.

Salary

Base: $137,344.80 - $206,017.20; Bonus/Equity: short-term incentive bonuses, equity-based awards; Benefits: qualified retirement programs, paid time off, health, dental, vision coverage

Skills & Requirements

Must-have

  • Quality Management System (QMS) oversight
  • ICH-GCP and GxP compliance
  • Risk-based quality and change control
  • Deviation and CAPA management
  • Quality SOP authoring and maintenance
  • Cross-functional quality improvement
  • Quality training and coaching

Nice-to-have

  • Experience with biomarker development
  • Human biological sample handling
  • Clinical trial sample lifecycle knowledge
  • Digital quality systems proficiency
  • Audit readiness and leadership
  • Collaborative team culture
  • Continuous improvement mindset

Key Requirements

  • Bachelor’s degree in sciences or equivalent experience
  • 5+ years pharmaceutical/biotech Quality Assurance experience
  • Strong knowledge of ICH-GCP and international regulations
  • Experience in risk-based quality and CAPA management
  • Ability to operate independently in matrix environment
  • Preferred Master’s degree in related field
  • 3+ years relevant biomarker or clinical trial experience

Work Rights

Not specified

Tailored Resume

Cover Letter