4-5

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.

Preparation of literature search reports and patent infringement analysis of the formulation strategies received from FnD team and third party APIs for different geographies.

Aurobindo Pharma Limited is an Indian multinational pharmaceutical manufacturing company headquartered in HITEC City, Hyderabad, India.

Responsible for operation and cleaning of Automatic visual inspection machine and labelling machine for DP. Preparation, review and execution of Study protocol / SOPs / QRM / Study report / QRM report in the drug product facility.

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.

Stability & validation samples analysis, OOS/OOT handling and documentation, GMP / GLP compliance & data integrity

Deviation and CAPA Support. Assist in documentation and tracking of deviations, change controls, and CAPAs. Participate in root cause analysis and follow-up actions.