To undertake production of lab, pilot batch, stability batch, trial batch, scale up batch of new products.
To prepare and update all documents i.e., specifications, process sheet, test methods, product manuals, procedure, batch manufacturing record (BMR), batch packaging record (BPR), process validation and instructions related to cGMP & ISO.
To work with QC & production team if face any problem in that respective area.
To develop the approved procedure, policies, and protocol in all levels of operation at co manufacturing unit.
To perform physical & chemical analysis of raw materials, packaging materials.
To updates intermediate products & finished goods time to time by internal resource and keep.
To minimizing the rejection or defects of finished goods by ensuring quality at each stage of production from PD respective during development any process.
To keep up to date of regulatory information like BDS, DGDA etc.
Any other task assigned by HoD as per department requirement.
Educational Requirements :
Bachelor of Pharmacy (B. Pharm), Master of Pharmacy (M. Pharm)