You will ensure the flow of stability samples and coordinate the execution of stability studies for externally manufactured products
Job Summary
You will ensure the flow of stability samples and coordinate the execution of stability studies for externally manufactured products.
You will prepare and verify documentation related to these studies, ensuring compliance with quality and regulatory requirements within a one-year contract.
Novartis offers a supportive and inclusive community focused on collaboration and innovation to improve patients' lives.
Matching Summary
You will ensure the flow of stability samples and coordinate the execution of stability studies for externally manufactured products.
Skills & Requirements
Must-have
Stability sample analysis coordination
GMP compliance adherence
Quality documentation management
Use of SAP/SLIM and Trackwise
Product quality assurance
Deviation and complaint investigation
Nice-to-have
Collaboration with technical operations and third parties
Digital savviness
Leadership
Problem solving skills
Communication skills
Data integrity
Dealing with ambiguity
Decision making
Regulatory requirements knowledge
Key Requirements
Higher education in Pharmacy, Chemistry, Medicine, Biology or related
Advanced English language proficiency
Minimum 6 months pharmaceutical industry experience
Knowledge of pharmaceutical quality control and production
Familiarity with GMP standards
Experience with Office Suite and digital quality tools
Work Rights
Must have right to work in Romania; no relocation support