Minimum 2 years in Quality Assurance within a Pharmaceutical company.
Job Role
- Responsible for Preparation/updation of SOPs and its final archival.
- Responsible to make sure relevant personnel trained on new SOPs/SOP revisions
- To prepare, review product quality reviews and archiving hard copies after the approval as per approved PQR Schedule.
- To initiate, notify internal and external change controls and to submit to QA Manager for its final closure and archive the relevant documentation.
- Responsible to prepare a monthly summary for the purpose of quality metrics.
- Responsible to review and manage complaints
- Performing QA reviews of batch documentation and appraisal of associated deviations and GMP investigations.
- Responsible to work on ad hoc projects and support Qualified Person as required.
Please contact Liam Smith from Science Solutions