Sr Engineer, Process Development

Amgen

Us
Base: 115,494.60usd - 156,257.40usd; bonus/equity:...
On-site
Biopharmaceutical manufacturing processes
Downstream purification
Process improvements
Amgen is seeking a Sr Engineer in Process Development to support their Drug Substance Technology group at their FleX Batch Biologics Manufacturing Facility. The ideal candidate should have extensive experience in biopharmaceutical manufacturing processes, particularly in downstream purification, and will play a critical role in developing process improvements and supporting regulatory activities

Job Summary

  • Amgen's shared mission to serve patients living with serious illnesses drives all that we do.
  • Apply fundamental scientific principles to Biopharmaceutical manufacturing processes (downstream purification) in the development of process improvements, facility adaptations, and new process operations.
  • In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities.

Matching Summary

Match Score: 85

Amgen is seeking a Sr Engineer in Process Development to support their Drug Substance Technology group at their FleX Batch Biologics Manufacturing Facility. The ideal candidate should have extensive experience in biopharmaceutical manufacturing processes, particularly in downstream purification, and will play a critical role in developing process improvements and supporting regulatory activities.

Salary

Base: 115,494.60USD - 156,257.40USD; Bonus/Equity: discretionary annual bonus program, stock-based long-term incentives; Benefits: comprehensive employee benefits package, Retirement and Savings Plan, group medical, dental and vision coverage, life and disability insurance, flexible spending accounts, award-winning time-off plans, flexible work models where possible

Skills & Requirements

Must-have

  • Biopharmaceutical manufacturing processes
  • downstream purification
  • process improvements
  • facility adaptations
  • new process operations
  • technical leadership
  • on-the-floor support
  • GMP manufacturing process tech transfer
  • evaluations
  • investigations
  • innovation
  • product life cycle management
  • regulatory filing
  • inspection
  • CMC activities
  • mammalian next generation technologies
  • increase yield
  • process robustness
  • enable new unit operations
  • biologics purification processes
  • chromatography
  • ultrafiltration
  • normal flow filtration operations
  • process scale-up
  • technology transfer
  • facility fit
  • PPQ support
  • MFG troubleshooting
  • complex investigation
  • engineering principles
  • statistical analysis
  • Quality by Design (QbD)
  • design of experiments (DoE)
  • verbal and written communication skills
  • interact effectively with diverse internal and external stakeholders
  • work in moderate direction
  • self-starter
  • take on several projects at one time

Nice-to-have

  • collaborative culture
  • science based
  • passion for challenges

Key Requirements

  • 10 years of biologics process development or commercial-scale technology transfer and technical support experience OR Associate’s degree and 8 years of biologics process development or commercial-scale technology transfer and technical support experience OR Bachelor’s degree and 4 years of biologics process development or commercial-scale technology transfer and technical support experience OR Master’s degree and 2 years of biologics process development or commercial-scale technology transfer and technical support experience OR Doctorate degree
  • 4+ years of experience in a Biotech/Pharma Process Development and/or Manufacturing Support role for drug substance manufacturing

Work Rights

Not specified

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