Parenteral Process Engineer: NPI & LCM Leader

Biopharma Careers

Schaffhausen

Vor Ort

CHF 120.000 - 180.000

Vollzeit

14 Tage+
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Zusammenfassung

Johnson & Johnson in Schaffhausen is seeking a Staff Process Engineer for Parenterals New Product Introduction & Life Cycle Management. You will lead technology transfer projects, introduce new products into commercial production, and implement new processes aligned with transfer plans and business objectives.

You will support inspections, regulatory filings, health authority responses, and ensure robust, compliant processing.

Qualifikationen

  • Bachelor’s degree in natural sciences or engineering required.
  • Master’s degree preferred.
  • 4+ years in pharmaceutical manufacturing or development.
  • Experience with parenteral products and manufacturing site operations.
  • Knowledge of SAP or PAS-X or similar systems.
  • Strong planning and logistics to integrate deliverables.

Aufgaben

  • Lead technology transfer projects for new product commercialization.
  • Prepare and execute engineering runs and validation batches.
  • Drive process improvements for robustness and compliance.
  • Manage change controls and documentation updates.
  • Train floor and leadership teams on project content.
  • Support audits and inspections as SME.
  • Collaborate with Production and other partners to align implementation.

Kenntnisse

Agile Manufacturing
CMC (Chemistry, Manufacturing, Control
Problem Solving
Data Analysis
Project Management
GMP Compliance
Quality mindset
Team Collaboration
Communication

Ausbildung

Bachelor’s degree in natural sciences or engineering
Master’s degree preferred

Tools

SAP
PAS-X

Jobbeschreibung

Johnson & Johnson in Schaffhausen is seeking a Staff Process Engineer for Parenterals New Product Introduction & Life Cycle Management. You will lead technology transfer projects, introduce new products into commercial production, and implement new processes aligned with transfer plans and business objectives.

You will support inspections, regulatory filings, health authority responses, and ensure robust, compliant processing.

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