Senior Specialist, Mts

Ferring B.V

Parsippany, New Jersey, US
Base: $76,831 to $142,685; bonus/equity: competiti...
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Cpv program management
Process and analytical technology transfer
Aseptic fill/finish drug product manufacturing
** Ferring B.V. is seeking a Senior Specialist in MTS for their Parsippany, New Jersey location, focusing on drug product technology transfer and regulatory compliance. The ideal candidate will possess a degree in a relevant scientific field and have at least three years of experience in the biopharmaceutical industry. **

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 process/analytical method improvements/optimizations, and authoring technical documents.
  • Ferring offers competitive total compensation, flexible benefits, tailored learning and development opportunities, and a 'People First' philosophy.

Matching Summary

Match Score: 75

** Ferring B.V. is seeking a Senior Specialist in MTS for their Parsippany, New Jersey location, focusing on drug product technology transfer and regulatory compliance. The ideal candidate will possess a degree in a relevant scientific field and have at least three years of experience in the biopharmaceutical industry. **

Salary

Base: $76,831 to $142,685; Bonus/Equity: Competitive annual incentive compensation targets; Benefits: Comprehensive healthcare, 401k plan and company match, disability coverage, life insurance, wellness benefits, tuition reimbursement, sick time, vacation time, 15 paid holidays, paid parental leave

Skills & Requirements

Must-have

  • CPV program management
  • Process and analytical technology transfer
  • Aseptic fill/finish drug product manufacturing
  • Technical document authoring and review
  • Design of experiment (DOE) studies
  • GMP or regulated laboratory environments

Nice-to-have

  • Entrepreneurial spirit
  • People first philosophy
  • Continuous improvement initiatives
  • Cross-functional collaboration

Key Requirements

  • Bachelor's degree in biology, biotechnology, chemical engineering, or related
  • 3+ years of relevant experience
  • Laboratory or manufacturing experience with biological/pharmaceutical/gene/cell therapy products
  • Experience supporting process development, analytical method development, or process monitoring
  • Experience with statistical analysis, data trending, or design of experiments (DOE)
  • Experience documenting experimental procedures, preparing technical reports, or maintaining laboratory documentation
  • Experience with process validation, technology transfer, or statistical analysis tools

Work Rights

Not specified

Tailored Resume

Cover Letter