Enrico Siegbrecht

Head of Department of Microbilogical Validation

Greifswald, Mecklenburg-West Pomerania, Germany

About

Experienced pharmaceutical Quality and Partner Management leader with a strong focus on External Manufacturing Network Management, CMO Oversight, and strategic partner governance. I specialize in building end-to-end oversight models for external manufacturing partners, integrating Quality, Supply, Risk & Compliance, and business perspectives into one structured governance framework. My work includes CMO classification, performance rating, KPI-based monitoring, BRM/QRM governance, supplier qualification, audits, recovery programs, and continuous improvement. I believe that effective CMO management goes beyond compliance. It requires transparency, cross-functional alignment, proactive risk management, and a partnership mindset to ensure product quality, supply continuity, and sustainable performance across the external manufacturing network.

Experience

  • CHEPLAPHARM (Full-time · 6 yrs 9 mos)
    • Senior Quality CMO Oversight Lead
      Oct 2025 - Present · 9 mos

    • Director Quality Assurance
      Jan 2024 - Oct 2025 · 1 yr 10 mos

    • Head of Quality Assurance
      Oct 2020 - Jan 2024 · 3 yrs 4 mos

  • IDT Biologika (Riems)
    • Head Of Quality Assurance
      Dec 2017 - Oct 2019 · 1 yr 11 mos

    • Manager Biological Testing & Hygiene Manager
      Jan 2016 - Nov 2017 · 1 yr 11 mos

      Teamleiter für die bakteriologische Qualitätskontrolle und Umgebungsmonitoring Hygienemanager für den Standort

  • Head of Department of Microbiological Validation at Vetter-Pharma Fertigung GmbH & Co. KG
    Jan 2013 - Dec 2015 · 3 yrs

  • Laborleiter F&E at Creatogen Laboratories GmbH
    2009 - 2011 · 2 yrs