I have performed the following works (prepare & update) and will reproduce them for others
* Validation Master Plan
* Site master File
* Quality manual ISO 9001:2015
* Risk analysis & reduction with FMEA
* Process validation
* Method validation
* Equipment qualification
* Cleaning Validation
* GMP training
* Calibration Schedule
* Preventive maintenance schedule
* QC test method for raw, packaging & finished product including microbiology
* Sampling for validation batch, Raw & packaging materials, the finished product
* sampling by AQL
* validation of Water treatment plant
* Protocol of Effluent treatment Plant
* Annual product quality review (APQR)
* implement Internal audit
* Incinerator
* Find out the root cause of complaints by layout/check sheet/ fishbone diagram/ scatter diagram
* Temperature mapping in warehouse
* To prepare all types of SOP ( AS per GMP guideline & mentioned above with relevant format etc.)
* Human drug formulation of the tablet, capsule, powder for suspension, semisolid, oral liquid, and external liquid
* Formulation of veterinary drug and feed supplement
* Implement QA system on the pharmaceutical proactive basis