Director Of Manufacturing

AstraZeneca

MA, United States
Base: $148,893.60 - $223,340.40 annual; bonus/equi...
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Cgmp manufacturing
Small molecule and peptide targeting moieties
Management of external vendors
** AstraZeneca is seeking a Director of Manufacturing to oversee the development and production of small molecules and peptides. The ideal candidate will possess extensive experience in GMP manufacturing, strong leadership skills, and the ability to manage external vendors in a fast-paced clinical environment. **

Job Summary

  • This individual will be responsible for leading the development and production of all small molecule and peptide targeting moieties (precursors) and linkers for the AZ portfolio.
  • The successful candidate will bring a strong background of GMP manufacturing and management of external vendors.
  • The annual base pay for this position ranges from $148,893.60 - $223,340.40 Annual USD.

Matching Summary

Match Score: 75

** AstraZeneca is seeking a Director of Manufacturing to oversee the development and production of small molecules and peptides. The ideal candidate will possess extensive experience in GMP manufacturing, strong leadership skills, and the ability to manage external vendors in a fast-paced clinical environment. **

Salary

Base: $148,893.60 - $223,340.40 Annual; Bonus/Equity: eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards; Benefits: medical & life insurance, annual bonus, education cost reimbursement, occasional allowances, anniversary awards, additional time off, pension plan, business travel insurance, recognition program, flexible working hours

Skills & Requirements

Must-have

  • cGMP manufacturing
  • small molecule and peptide targeting moieties
  • management of external vendors
  • process development and manufacturing
  • analytical methods and specifications
  • CMC regulatory environment

Nice-to-have

  • collaborative skills
  • multi-tasking ability
  • fast-paced environment
  • clinical stage company
  • strategic partnerships

Key Requirements

  • PhD or MS with 10+ years of experience
  • cGMP Manufacturing experience in small molecules/peptides
  • proven track record leveraging and managing CRO/CDMOs

Work Rights

Not specified

Tailored Resume

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