Pithampur

Topical Formulation, Semi Solid Manufacturing, Cream Ointment Gel Production, QMS, SAP, In Process Checks, Deviation Handling and CAPA, Audit readiness and documentation, Production Planning and Scheduling, Cross functional collaboration, Team Supervision, Process Optimization.

Candidate should have strong understanding of OSD manufacturing processes and knowledge of cGMP and relevant regulatory requirements. Monitoring critical process parameters during manufacturing. Candidate should have sound knowledge of QMS - Incidents, Change control, Deviations etc. Should be able to handle the team of 8-10 persons

HPLC, GC, Physical and Chemical Analysis, QMS,RM,PM. Material Dispensing, RM Store, FG Store, Environment Monitoring, SAP, Inventory, QMS

Day-to-day production activities, Machine operation, GMP Compliance. Exposure to Topical products like; Cream, Lotion, Gel Manufacturing and packing and its documentation. Good Communication, Presentation and Man Management skills.

M. Pharma / B. Pharma; Awareness of regulatory requirement, ANDA filing & new Product filing application, Handle Field Alert Report, Market complaint, Review & presentation of Data, Tracking of data. Planning for sample pullout, Batch charging, storage & reconciliation, destruction & smooth functioning of Stability chamber, Walk-in Chamber

M.Sc / B.Pharm / M.Pharm. Material Dispensing, Ointment, Gel Manufacturing, Filling, Packing, Track and Trace, Labelling, Cartonator, QMS. IPQA, Document Cell, OOS, OOT, Process/ Cleaning Validation, Review of BMR & BPR, Training ,QMS Investigation, CAPA, SOPs etc.

Candidates having hands-on experience in Analysis of Raw Material, Packaging Material, Finished Goods, Stability, Method Transfer and Laboratory Investigations. Should have sound knowledge of QMS like Deviations, Change Control, Vendor Management etc.

IPQA, Document Cell, Market Complaints, Market Recall, 00S, 00T, Process, Cleaning Validation, Review of BMR & BPR, Training, QMS.

Line Clearance, Material verification, environment monitoring, in-process checks, Terminal inspection, online CPV entries & process validation challenges & batch record review.