Engineer TH-C747

Quality & regulatory engineer · Lead / Expert (10+ years)

Quality & Compliance Lead – Pharmaceutical Sciences, CDMO Biologics, cGMP

Skills and tools

  • cGMP
  • QMS
  • Deviations
  • Complaints
  • Root Cause Analysis
  • OOx investigations
  • CAPA
  • change controls
  • Quality Risk Management
  • SOP authorship and review
  • Supplier quality
  • Audit support

Languages

DE B2/B1 · EN C2/C2 · FR native/native · CH-DE speaks/understands · IT C2/C2

Work experience

  1. 2021 – 2026

    Compliance Lead Third Party Analytical Services

    CDMO in the biologics sector, mid-size, Basel site

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Tasks, schools and dates after login

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  1. 2012 – 2021

    ADME/Safety Specialist (Enzymology and Transporters)

    Global pharmaceutical corporation, 10'000+ employees, pharmaceutical sciences R&D division

  2. 1997 – 2012

    Physico-Chemical Assay Development Responsible

    Global pharmaceutical corporation, 10'000+ employees, non-clinical safety research division

Education & further training

  1. Engineer Degree (Master in Chemistry) Chemistry

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