Senior Specialist, Mts

ferring.co.kr

Parsippany, New Jersey, US
Base: $76,831 to $142,685; bonus/equity: annual bo...
Drug product technology transfer
Continuous process verification (cpv) program
Statistical analysis and design of experiments (doe)
Ferring pioneers and delivers life-changing therapies that help people build families and live better lives while maintaining an entrepreneurial spirit and a people-first philosophy

Job Summary

  • Ferring pioneers and delivers life-changing therapies that help people build families and live better lives while maintaining an entrepreneurial spirit and a people-first philosophy.
  • The Senior Specialist, MTS is responsible for supporting aseptic drug product manufacturing through technology transfer, process improvements, and regulatory compliance at the US Production site.
  • Ferring offers competitive total compensation, comprehensive benefits, flexible working hours, and a culture recognized as one of the best places to work in the country.

Matching Summary

Ferring pioneers and delivers life-changing therapies that help people build families and live better lives while maintaining an entrepreneurial spirit and a people-first philosophy.

Salary

Base: $76,831 to $142,685; Bonus/Equity: Annual bonus based on individual and company performance; Benefits: Comprehensive healthcare, 401k with company match, disability coverage, paid time off, and parental leave

Skills & Requirements

Must-have

  • Drug product technology transfer
  • Continuous process verification (CPV) program
  • Statistical analysis and design of experiments (DOE)
  • Aseptic fill/finish manufacturing support
  • Process and analytical method improvements
  • Regulatory compliance in GMP environments

Nice-to-have

  • Lean Six Sigma continuous improvement
  • Cross-functional collaboration
  • Strong written and verbal communication
  • Experience with process validation
  • Use of statistical analysis tools (JMP, Minitab)

Key Requirements

  • Bachelor’s degree in biology, biotechnology, or related field
  • 3+ years relevant biopharmaceutical or laboratory experience
  • Experience with aseptic techniques and sterile processing
  • Knowledge of GMP or regulated laboratory environments
  • Experience with process development and analytical method support

Work Rights

Not specified

Tailored Resume

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