Process Development Sr Scientist

Amgen

Thousand Oaks, California, United States
Base: $126,066.05 - $170,559.95 usd; bonus/equity:...
Not specified (assumed onsite).
Doctorate degree in life sciences
Analytical chemistry or biochemistry expertise
Hplc and ce method development experience
Amgen is seeking a Process Development Senior Scientist to join its Attribute Sciences department in Thousand Oaks, California. The role involves providing strategic analytical leadership and technical support in the development of manufacturing processes for various therapeutic modalities, with a strong emphasis on collaboration and innovation

Job Summary

  • This role involves defining favorable quality characteristics and optimizing analytical tools to guide the development of robust manufacturing processes for various therapeutic modalities.
  • The successful candidate will supervise a team, act as an Attribute Sciences Team Lead, and drive product characterization for process comparability studies and regulatory filings.
  • Amgen offers a comprehensive benefits package including retirement plans, health coverage, stock incentives, and flexible work models to support professional growth.

Matching Summary

Match Score: 85

Amgen is seeking a Process Development Senior Scientist to join its Attribute Sciences department in Thousand Oaks, California. The role involves providing strategic analytical leadership and technical support in the development of manufacturing processes for various therapeutic modalities, with a strong emphasis on collaboration and innovation.

Salary

Base: $126,066.05 - $170,559.95 USD; Bonus/Equity: Discretionary annual bonus and stock-based long-term incentives; Benefits: Comprehensive health, dental, vision, retirement plan, and flexible time-off

Skills & Requirements

Must-have

  • Doctorate degree in life sciences
  • Analytical chemistry or biochemistry expertise
  • HPLC and CE method development experience
  • Regulatory filing authoring experience
  • GMP and GLP compliance knowledge

Nice-to-have

  • Experience with live oncolytic viruses
  • Cross-functional leadership skills
  • Protein-based therapy characterization
  • Contract manufacturing site management

Key Requirements

  • Doctorate degree OR Master's with 2 years experience
  • 5-7+ years in Analytical Chemistry or Biochemistry
  • Proficiency in HPLC and CE methods
  • Knowledge of regulatory requirements and guidelines
  • Understanding of Good Laboratory Practices (GLP) and GMP

Work Rights

Not specified

Tailored Resume

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