Director of Technical Support – Pilot Plant Operations

Novo Nordisk

Gladsaxe Kommune

On-site

DKK 941,000 - 1,449,000

Full time

2 days ago
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Job summary

Novo Nordisk seeks a visionary Director of Technical Support for CMC API Pilots DK to lead a cross-functional team delivering excellent support for drug substance and pilot plant operations in Bagsværd and Gentofte. You will set strategic direction, build leadership capacity, and drive world‑class pilot operations to enable clinical trial material delivery.

You will lead with conviction, manage complex priorities, and ensure efficient collaboration across CMC Development, Regulatory Affairs, and

Qualifications

  • A relevant scientific or technical Master’s degree (or higher).
  • Proven leadership experience at senior level, preferably in CMC/pharmaceutical development.
  • Strong business understanding of R&D processes and pharmaceutical quality standards.
  • Proven ability to set direction and lead through change in complex environments.
  • Excellent communication skills and high personal integrity in multi-stakeholder settings.

Responsibilities

  • Lead and develop a high‑performing organisation with clear expectations and modern leadership.
  • Ensure timely delivery of high‑quality drug product to clinical trials and development programmes.
  • Set direction and lead through change, balancing speed, quality, and risk.
  • Build a scalable leadership team with clear accountability across four teams.
  • Collaborate across CMC Pilots and with Regulatory Affairs, Global MFG & Supply, and Quality.

Skills

Leadership
English fluency
Strategic thinking
Change management
Cross-functional leadership

Education

Master’s degree or higher

Job description

Novo Nordisk seeks a visionary Director of Technical Support for CMC API Pilots DK to lead a cross-functional team delivering excellent support for drug substance and pilot plant operations in Bagsværd and Gentofte. You will set strategic direction, build leadership capacity, and drive world‑class pilot operations to enable clinical trial material delivery.

You will lead with conviction, manage complex priorities, and ensure efficient collaboration across CMC Development, Regulatory Affairs, and

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