Head Of Centre Of Expertise Aseptic Processes & Global Technical Operations- Manufacturing Technology & Science

Ferring B.V

Kiel, Germany
**
Global standards for aseptic practices
Process standardization and lifecycle management
Technical stewardship and technology transfer support
** Ferring B.V. is seeking a Head of Centre of Expertise for Aseptic Processes within its Global Technical Operations division in Kiel, Germany. The ideal candidate will manage a team of experts to establish global standards for aseptic practices, and will require significant experience in the pharmaceutical industry, particularly in aseptic manufacturing. **

Job Summary

  • You will be responsible for managing a team of experts establishing and leading global standards and capabilities for aseptic practices across the network.
  • The mission includes process standardization, lifecycle management, technical stewardship, technology transfer support, and global capability.
  • Ferring Pharmaceuticals helps people around the world build families and live better lives through scientific advances.

Matching Summary

Match Score: 75

** Ferring B.V. is seeking a Head of Centre of Expertise for Aseptic Processes within its Global Technical Operations division in Kiel, Germany. The ideal candidate will manage a team of experts to establish global standards for aseptic practices, and will require significant experience in the pharmaceutical industry, particularly in aseptic manufacturing. **

Skills & Requirements

Must-have

  • global standards for aseptic practices
  • process standardization and lifecycle management
  • technical stewardship and technology transfer support
  • global capability for aseptic processes
  • risk assessment and validation strategy

Nice-to-have

  • scientific advances in health
  • empowerment and speaking up culture
  • collaboration and continuous improvement

Key Requirements

  • Master’s or PhD in Engineering, Chemistry, Pharmaceutical Technology, Analytical Chemistry, Bioprocessing, or related field
  • 5+ years of experience in pharmaceutical/biotech/chemical industry
  • Strong experience with GMP, regulatory requirements, data integrity, and CMC lifecycle management

Work Rights

Not specified

Tailored Resume

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