Senior Scientist, Downstream Process Tech (GMP)

Incyte

Yverdon-les-Bains

Vor Ort

CHF 140.000 - 190.000

Vollzeit

vor 47 Stunden
Sei unter den ersten Bewerbenden
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Zusammenfassung

Incyte is seeking a Senior Scientist/Engineer, Downstream Manufacturing Technology, to lead technology transfers and support new product introductions at the Yverdon Bioplant. The role serves as the downstream SME for GMP manufacturing and collaborates across Production, QA, QC, Engineering, and Process Science.

You will drive process description definitions, MES alignment, and risk assessments, while guiding investigations, validations, and continuous improvement initiatives in a fast-paced

Qualifikationen

  • MSc or equivalent in biotech, biochem, or related field.
  • Extensive biopharma manufacturing and MSAT experience, GMP preferred.
  • Experience with technology transfer and downstream processing.

Aufgaben

  • Lead downstream technology transfers for new products at Yverdon Bioplant.
  • Assess facility fit, scalability, and readiness for incoming downstream processes.
  • Provide downstream expertise during GMP campaigns and troubleshoot.
  • Lead investigations, deviations, and process validation activities.
  • Develop and review DSP documentation and GMP reports.
  • Collaborate with QA/QC, Process Science, and Production.
  • Drive continuous improvement and risk management initiatives.

Kenntnisse

Downstream manufacturing
MSAT
Process development
Technology transfer
GMP expertise
DOE
FMEA
Statistical analysis

Ausbildung

MSc or equivalent in biotech/biochem/chemical engineering

Jobbeschreibung

Incyte is seeking a Senior Scientist/Engineer, Downstream Manufacturing Technology, to lead technology transfers and support new product introductions at the Yverdon Bioplant. The role serves as the downstream SME for GMP manufacturing and collaborates across Production, QA, QC, Engineering, and Process Science.

You will drive process description definitions, MES alignment, and risk assessments, while guiding investigations, validations, and continuous improvement initiatives in a fast-paced

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