This role combines high responsibility for GMP compliance and quality standards with cross-department collaboration to impact production safety and efficiency
Job Summary
This role combines high responsibility for GMP compliance and quality standards with cross-department collaboration to impact production safety and efficiency.
Takeda offers an attractive compensation package including hybrid work, 30 vacation days, health programs, and a long-term incentive plan.
The Singen site is a diverse and certified great place to work, specializing in pharmaceutical manufacturing with excellent development opportunities.
Matching Summary
This role combines high responsibility for GMP compliance and quality standards with cross-department collaboration to impact production safety and efficiency.
Skills & Requirements
Must-have
GMP compliance and quality standards
Engineering team leadership and management
Qualification and validation expertise
Cross-functional collaboration
Technical documentation and audit readiness
Nice-to-have
Strategic thinking and process orientation
Stakeholder management skills
Digitalization and standardization initiatives
Fluent German and English communication
Experience with TrackWise and document management systems
Key Requirements
Engineering degree in relevant field
5-7 years pharmaceutical or regulated industry experience
Minimum 3 years leadership experience
Expertise in GMP, IQ/OQ/PQ, FDA and EMA regulations
Experience with qualification and validation processes