Compression, Coating, Granulation & Blending. Maintaining BMR of Solid dosage form and related logbooks during process, production activities in line with cGMP norms and applicable SOPs.
Execution of qualification / validation for equipment, utility and facility. Preparation & review of qualification protocols and handling change controls.
Experience in pharma industry for handling shift-related activities like work schedule, release of in-process and intermediate samples etc. Natco Pharma
Micro Labs inviting B.Pharm/M. Pharm / M.Sc for Handling of batch manufacturing and filling activity with regulatory exposure (3 Piece, BFSeye drops and Injectable) in Sterile area.
Experiences in HPLC/ GC/ IR/ UV/ Dissolution/ Polarimeter/ Potentiometric titrations/ KF/ PSD by Malvern. Awareness on current Data Integrity requirements & cGMP requirements. Stability studies
Ability to collaborate effectively with cross-functional teams, including R&D, marketing, sales, finance, and regulatory affairs, to achieve project objectives and deliver end to end results.