We are looking for a Validation Expert who is passionate about quality and process excellence to ensure robust validation across the full lifecycle at our Kurtköy site
Job Summary
We are looking for a Validation Expert who is passionate about quality and process excellence to ensure robust validation across the full lifecycle at our Kurtköy site.
The role involves leading validation planning, maintaining GMP compliance, driving ongoing process verification, and ensuring inspection readiness through strong technical expertise and documentation.
Novartis is committed to building an outstanding, inclusive work environment and offers various benefits to help associates thrive personally and professionally.
Matching Summary
We are looking for a Validation Expert who is passionate about quality and process excellence to ensure robust validation across the full lifecycle at our Kurtköy site.
Skills & Requirements
Must-have
Process validation lifecycle management
GMP compliance and quality systems
Technical report writing and review
Ongoing process verification (OPV)
Cross-functional team collaboration
Inspection readiness and deviation management
Nice-to-have
Risk management and pre-validation assessments
Quality risk management
High-quality documentation standards
Strong technical expertise
Commitment to diversity and inclusion
Lean manufacturing principles
Key Requirements
Bachelor’s degree in Chemistry, Pharmacy, Chemical Engineering, Pharmaceutical Technology or related field
2–3 years pharmaceutical manufacturing or quality experience
Fluent in English and local site language
Experience with process validation and technical report writing