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.
• Identification, selection and management of Contract Development & Manufacturing Organizations (CDMOs) for process optimization, cGMP manufacture of Precursors in support of ongoing clinical programs and subsequent commercial supply in compliance with cGMP, ICH and FDA regulations.
• The annual base pay for this position ranges from $ 148,893.60 - $223,340.40 Annual USD.

Matching Summary

Salary

Base: $148,893.60 - $223,340.40 Annual USD; 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, qualified retirement programs, paid time off, health, dental, and vision coverage

Skills & Requirements

Key Requirements

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

Work Rights