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General Manager – Pharmaceutical Manufacturing Site

Mantell Associates

Senior 🇬🇧 English
Lean Manufacturing GMP regulations Continuous Improvement

Job description

About the role

The client, a leading CDMO, is seeking an experienced General Manager to lead a strategically important manufacturing site in Germany. This senior leadership position holds full responsibility for site performance, operational excellence, commercial success, and long‑term growth.

Key responsibilities

  • Lead all site functions including manufacturing, engineering, supply chain, continuous improvement and EHS.
  • Develop and execute site strategy aligned with corporate goals and growth plans.
  • Drive Lean manufacturing and continuous improvement initiatives to raise operational excellence.
  • Ensure compliance with GMP, quality standards and health, safety and environmental regulations.
  • Build, develop and mentor a high‑performing leadership team and succession pipeline.
  • Collaborate with commercial teams to meet customer expectations and retain business.
  • Own site financial performance, including P&L, budgeting, forecasting and cost management.
  • Monitor operational and financial KPIs and implement actions to improve productivity and profitability.

Required profile

  • Degree in Engineering, Pharmaceutical Sciences, Operations Management, Chemistry or related field; advanced qualifications preferred.
  • Extensive leadership experience in pharmaceutical manufacturing, CDMO or regulated life‑sciences environments.
  • Proven track record of leading large‑scale operations with measurable improvements and full P&L accountability.
  • Strong commercial awareness and ability to translate business objectives into operational execution.
  • Fluent in German and English and willing to be site‑based in Germany.

Required skills

  • Lean Manufacturing
  • GMP regulations
  • Continuous Improvement

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Published 3 months ago

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Mantell Associates