Senior Production Engineer, Fractionation

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5+ years pharmaceutical manufacturing experience
Aseptic and fractionation processing expertise
Root cause analysis and capa implementation
** The Senior Production Engineer role at CSL Behring focuses on providing engineering support to pharmaceutical manufacturing operations, particularly in fractionation processes. Candidates are expected to lead maintenance strategies, ensure compliance with industry standards, and mentor junior engineers, while also being involved in continuous improvement initiatives. **

Job Summary

  • The Senior Production Engineer provides technical leadership to ensure optimal asset performance and compliance throughout the pharmaceutical asset lifecycle.
  • This role drives risk-based asset management strategies aligned with ISO 55000 principles and GMP requirements while partnering with cross-functional teams.
  • CSL Behring is a global biotherapeutics leader committed to saving lives through innovative therapies derived from plasma fractionation and recombinant protein technology.

Matching Summary

Match Score: 75

** The Senior Production Engineer role at CSL Behring focuses on providing engineering support to pharmaceutical manufacturing operations, particularly in fractionation processes. Candidates are expected to lead maintenance strategies, ensure compliance with industry standards, and mentor junior engineers, while also being involved in continuous improvement initiatives. **

Skills & Requirements

Must-have

  • 5+ years pharmaceutical manufacturing experience
  • Aseptic and fractionation processing expertise
  • Root cause analysis and CAPA implementation
  • GMP and ISO 55000 compliance knowledge
  • SAP CMMS data analysis skills

Nice-to-have

  • Six Sigma or Lean principles knowledge
  • Mentoring junior engineers and technicians
  • Strategic planning and execution capabilities
  • Cross-functional collaboration experience

Key Requirements

  • Bachelor's degree in Engineering
  • Master's degree preferred
  • Proven experience supporting cGMP environments
  • Strong knowledge of sterile filling operations

Work Rights

Not specified

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