Job Summary

• This leader will own end‑to‑end CDMO partnerships aligning external execution with AstraZeneca’s business objectives to deliver reliable, cost‑effective supply and technical robustness across preclinical, clinical, and commercial stages.
• Partner with QA to ensure GMP compliance at CDMOs, support audits, investigations, and CAPAs, and maintain alignment with global regulations and evolving guidance for viral vectors and plasmids.
• The annual base pay for this position ranges from $ 180,740.80 - 271,111.20.

Matching Summary

Salary

Base: $180,740.80 - $271,111.20; Bonus/Equity: short-term incentive bonus opportunity, equity-based long-term incentive program; Benefits: 401(k) plan, paid vacation and holidays, paid leaves, health benefits (medical, prescription drug, dental, vision)

Skills & Requirements

Key Requirements

• 10+ years in biopharmaceuticals
• 5+ years managing external manufacturing/CDMOs
• Advanced degree (PhD or MS preferred)
• Proven track record of tech transfer
• Familiarity with cost modeling

Work Rights