- Responsible for overall quality of products and compliance of GMP at the site.
- Line clearance prior to dispensing, manufacturing, packing and validation activity.
- Sampling during manufacturing of validation, exhibit and commercial batches.
- In process control, routine inspection and online process verification and documentation.
- Preparation, review and approval of documents such as SOP, BMR, BPR, SMF, VMP, APQR, MFR validation protocols/report and qualification protocols/report.
- Execution and evaluation of qualification and validation studies.
- To evaluate and authorize rework or reprocessing of the batch.
- To review batch documentation and release the batches for distribution.
- To involve in quality control functions to ensure GLP and data authenticity.
- Review and approval of work sheet, COA, raw and packing material specification, semi- finished specification, finished product specification and stability protocol.
- To review stability data generated at site and submit to RA for dossier preparation.
- To control, distribute, retrieve and destruction of the master and executed documents such as BMR, BPR, analytical work books, master SOPs, protocols, reports, log books.
Job Types: Full-time, Permanent
Pay: From ₹14,000.00 per month
Work Location: In person
