Long Description

1             Exposure of execution of planning of Inprocess, Finished product, stability and cleaning validation samples of

MDI / DPI formulation.

2             Exposure of compliance to all cGMP, GxP or any other regulatory requirements, including EHS requirements.

3             Maintenance of GLP in the Laboratory.

4             Having knowledge of Analytical Instruments like HPLC, GC, GCMS, LCMS, UV, IR, KF, ACI, NGI, DUSA, Spray Pattern etc.

5             Exposure of Laboratory investigation like OOS, OOT, Incidence, Deviation, CAPA, Change control etc.

6             Exposure of Stability sample management & Regulatory Audits.

7             Exposure of Analytical method transfer, Analytical method validation / Verification activity.

8             Exposure of Calibration of Analytical Instruments & Equipment’s

9             Compliance to observation noted during internal and external audits.

Competencies Strategic AgilityProcess ExcellenceCollaborationInnovation & CreativityResult OrientationStakeholder ManagementCustomer CentricityDeveloping TalentEducation Graduation in PharmacyWork Experience

10 to 15 years.