Quality Documentation Specialist - determined period of time
Zentiva(3 months ago)
About this role
A Quality Documentation Specialist at Zentiva supports pharmaceutical product quality by managing and maintaining specification and quality documentation to ensure compliance with internal procedures and regulatory requirements. The role operates within a manufacturing and regulatory environment, contributing to product registration readiness and quality assurance processes.
Required Skills
- Specification Writing
- LIMS
- Document Control
- Change Control
- Compliance
- Excel
- SAP
- Database Management
- English
- Communication
Qualifications
- University Degree in Chemistry
- University Degree in Biochemistry
- University Degree in Pharmacy
About Zentiva
zentiva.comWe develop, produce, and deliver high-quality, affordable medicines to more than 100 million people across Europe.
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