Head Of Quality Assurance

Takeda

Lessines, Belgium
Not specified (assumed to be on-site given the nature of the role).
Cgmp compliance
Global regulatory requirements
Biopharmaceutical manufacturing
Takeda is seeking a Head of Quality Assurance for its Lessines, Belgium site, responsible for leading QA operations within a complex biopharmaceutical manufacturing environment. The ideal candidate will possess extensive experience in GxP-regulated settings, strong leadership skills, and a deep understanding of regulatory compliance

Job Summary

  • Lead the QA organization of >90 employees, providing quality oversight across Purification, Aseptic Filling, Packaging, Warehousing, and Shipping, including site sterility assurance governance and batch disposition for marketed and clinical products.
  • Champion compliance and be accountable for implementation by influencing cross-functional partners to adopt and follow applicable regulatory requirements, Quality Systems and Global and Local procedures.
  • We offer a comprehensive benefits package, prioritizing wellbeing, career growth, and work-life balance: Generous Time Off, Health & Wellbeing, Family Support, Career Development, Transportation & Eco-Benefits, Additional Perks.

Matching Summary

Match Score: 85

Takeda is seeking a Head of Quality Assurance for its Lessines, Belgium site, responsible for leading QA operations within a complex biopharmaceutical manufacturing environment. The ideal candidate will possess extensive experience in GxP-regulated settings, strong leadership skills, and a deep understanding of regulatory compliance.

Skills & Requirements

Must-have

  • cGMP compliance
  • global regulatory requirements
  • biopharmaceutical manufacturing
  • quality oversight
  • batch disposition
  • risk-based decision-making

Nice-to-have

  • transformational agility
  • digital solutions
  • operational excellence
  • collaboration
  • innovation

Key Requirements

  • Master’s degree in pharmaceutical, chemical, biological, or technical sciences
  • 10+ years of experience in GxP-regulated pharmaceutical or biotech
  • Proven people leadership experience
  • Strong knowledge of cGMP, FDA CFR, EU GMP
  • Fluent in English and French

Work Rights

Not specified

Tailored Resume

Cover Letter