Senior Specialist, Mts

Ferring Com Ar

Parsippany, New Jersey, US
Base: $76,831 to $142,685; bonus/equity: competiti...
Cpv program management
Aseptic fill/finish manufacturing
Process/analytical method improvements
The Senior Specialist, MTS is accountable for functional, technical, and business objectives and supports project execution for drug product technology transfer, continuous improvement, and regulatory compliance at the US Production site

Job Summary

  • The Senior Specialist, MTS is accountable for functional, technical, and business objectives and supports project execution for drug product technology transfer, continuous improvement, and regulatory compliance at the US Production site.
  • Responsibilities include maintaining and expanding the CPV program, supporting aseptic fill/finish drug product manufacturing, authoring technical documents, and executing technical/engineering studies.
  • Ferring offers competitive total compensation, exceptional flexible benefits, personal support, and tailored learning and development opportunities, fostering a 'People First' philosophy.

Matching Summary

The Senior Specialist, MTS is accountable for functional, technical, and business objectives and supports project execution for drug product technology transfer, continuous improvement, and regulatory compliance at the US Production site.

Salary

Base: $76,831 to $142,685; Bonus/Equity: Competitive annual incentive compensation targets; Benefits: Comprehensive healthcare, 401k, disability, life insurance, wellness, tuition reimbursement, sick time, vacation time, paid holidays, paid parental leave

Skills & Requirements

Must-have

  • CPV program management
  • Aseptic fill/finish manufacturing
  • Process/analytical method improvements
  • Technology transfer execution
  • Technical document authoring
  • Design of experiment (DOE) studies

Nice-to-have

  • Entrepreneurial spirit
  • People first philosophy
  • Cross-functional collaboration
  • Lean Six Sigma program support

Key Requirements

  • Bachelor's degree in biology, biotechnology, chemical engineering, or related scientific discipline
  • 3+ years of relevant experience
  • Laboratory or manufacturing experience with biological, pharmaceutical, or gene/cell therapy products
  • Experience supporting process development, analytical method development, or process monitoring
  • Familiarity with GMP or other regulated laboratory environments

Work Rights

Not specified

Tailored Resume

Cover Letter