Bachelor of Science / Master of Science, having minimum 1-2 years of experience in the pharmaceutical industryCompetences
- Very good spoken and written communication skills in the English language
- Practical experience of preparation & handling of documents related to the Quality Management System.
- Handling of software-based documentation system will be considered as added advantage.
- Well versed with MS office (latest versions)
- Independent working with minimal supervision
- Adequately maintaining the Documents Management System (i.e. to prepare, maintain, control, issue & archival) as per Quality Management System requirement in the electronic system.
- Support for QMS deployment, FDA related activities
- Stability study report preparation
- Support to validation/qualification activities
- APQR data compilation
Supporting to others as required for Quality System & Quality ComplianceLocations
Fixed Term (Fixed Term)Time Type