Director Discovery Process And Analytical Development

AstraZeneca

**
12+ years postgraduate industry experience
Lentiviral vector manufacturing expertise
Gmp and analytical development leadership
** AstraZeneca is seeking a Director of Discovery Process and Analytical Development to lead the strategy for early process development and analytical methods for novel in vivo lentiviral vectors. The successful candidate will drive innovation in cell and gene therapy, collaborating across teams to ensure compliance with regulatory standards and operational excellence. **

Job Summary

  • This role involves leading the strategy for adapting EsoBiotec's R&D vectors to bioreactor manufacturing and engineering new production cell lines.
  • The successful candidate will serve as a senior representative in cross-functional teams to shape comprehensive CMC strategies and ensure regulatory readiness.
  • You will direct vector manufacturing and quality testing at external CDMOs while establishing governance, oversight, and compliance frameworks.

Matching Summary

Match Score: 75

** AstraZeneca is seeking a Director of Discovery Process and Analytical Development to lead the strategy for early process development and analytical methods for novel in vivo lentiviral vectors. The successful candidate will drive innovation in cell and gene therapy, collaborating across teams to ensure compliance with regulatory standards and operational excellence. **

Skills & Requirements

Must-have

  • 12+ years postgraduate industry experience
  • Lentiviral vector manufacturing expertise
  • GMP and analytical development leadership
  • CDMO oversight and management
  • CMC regulatory guideline fluency

Nice-to-have

  • Passion for gene therapy innovation
  • Strong stakeholder communication skills
  • Collaborative cross-functional mindset
  • Experience with in vivo cell therapies

Key Requirements

  • MSc or PhD in Virology, Biochemistry, Cell Biology, Molecular Biology, Biomedical Engineering, or related discipline
  • 12+ years of postgraduate industry experience in manufacturing (including GMP) and analytical development
  • Proven track record leading process and analytical development teams
  • Familiarity with CMC regulatory guidelines for gene or cell therapy products

Work Rights

Not specified

Tailored Resume

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