Posted:16 hours ago|
Platform:
Work from Office
Full Time
1. Preparation and Review of AQA SOPs.
2. Review of validation protocols & reports.3. Review of completed laboratory control records.4. Making sure that effective systems are used for calibrating critical instruments.5. Review of changes that potentially impact product quality.6. Review of incidents / deviations and ensuring that they are resolved and closed with adequate CAPA.7. Performing general system reviews.8. Ensuring the implementation of continuous training program to departmental personnel as per established procedures.9. Issue and Retrieval of Formats, Protocols, Reports and Relevant records.10. Responsible for archival of GMP documents.
MSN Group
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