Manage sample storage and inventory to ensure traceability and integrity.
Perform analytical testing and maintain documentation for API, drug substances, drug products, finished products, complaints, stability, and packaging material samples.
Ensure all laboratory activities comply with cGxP standards, including data integrity requirements.
Support stability studies including testing, sample management, and documentation in accordance with cGxP standards.
Adhere to all HSE policies, guidelines, and best practices.
Identify, report, and propose solutions for potential accidents and risks.
Requirements
Diploma in Chemistry / Pharmaceutical Science with relevant laboratory experience
2-3 years of experience working in a pharmaceutical laboratory environment
