Process Development Senior Associate

Amgen Inc

Base: $80,044.50 - $108,295.50 usd annually; bonus...
Not specified (potentially hybrid or onsite based on typical biotech industry practices)
Master's degree or equivalent experience
Hands-on formulation laboratory experience
Knowledge of gmp and cgmp requirements
Amgen Inc. is seeking a Process Development Senior Associate to join their Oral and Enabling Delivery Systems group, focused on developing oral solid dosage forms for early-stage clinical programs. The position requires strong laboratory experience and collaboration skills, with an emphasis on process development and experimental design

Job Summary

  • The role involves executing formulation and process development experiments for oral solid dosage forms within the Drug Product Technologies group.
  • Candidates must independently plan and execute routine material characterization studies while contributing to experimental design.
  • Amgen offers a comprehensive benefits package including retirement plans, health coverage, and stock-based long-term incentives.

Matching Summary

Match Score: 85

Amgen Inc. is seeking a Process Development Senior Associate to join their Oral and Enabling Delivery Systems group, focused on developing oral solid dosage forms for early-stage clinical programs. The position requires strong laboratory experience and collaboration skills, with an emphasis on process development and experimental design.

Salary

Base: $80,044.50 - $108,295.50 USD annually; Bonus/Equity: Discretionary annual bonus and stock-based incentives; Benefits: Comprehensive health, dental, vision, and retirement plans

Skills & Requirements

Must-have

  • Master's degree or equivalent experience
  • Hands-on formulation laboratory experience
  • Knowledge of GMP and cGMP requirements

Nice-to-have

  • Experience with oral solid dosage forms
  • Strong written and verbal communication skills
  • Ability to manage multiple priorities

Key Requirements

  • Master's degree OR Bachelor's with 2 years experience
  • 2+ years pharmaceutical industry experience preferred
  • Working knowledge of pharmaceutical development in GMP environment

Work Rights

Not specified

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