Madhya Pradesh

Exposure on technology transfer from lab to pilot & commercial scale. Efficient management of Plant Operations including Men, Material & Machine management in order achieve the best operational efficiency of the Plant.

M.Sc, M.Pharma, B.Pharma. Working in QC analyzing, Stability. In process. FP. RM sample. Handling instruments like HPLC. GC. FTIR. UV, DR. SSA. etc. versatile In handling SAP. documentation like preparing STPs and review of analytical hard copies and electronic data.

Officers under the Central, State, U.T. Governments, Universities, Statutory Bodies, Autonomous Bodies or Research and Development Organizations Holding analogous posts on regular basis.

Finished area Adhere to Safety and CGMP Norms, Distillation, Layer Separation, Solvent Handling, SRP, Hydrogenation, Micronization, DCS Automation

Craft and maintain BPCRs and SOPs with precision, Lead documentation management using EDMS to uphold data integrity and compliance, Drive training and compliance efforts through our LMS, Ensure all production documentation aligns with regulatory standards and internal policies.

Production QMS Quality Management System Handling of QMS activities like Deviation, Incident, Investigation, CCP, Protocol Preparation, Risk Assessment etc.

Experiences in HPLC, GC, LCMS, GCMS, IR, UV, Dissolution, Polarimeter, Potentiometric titrations, KF, PSD by Malvern and Other wet & Physical analysis

M.Pharm, B.Pharm, M.Sc, B.Sc, ITI, Diploma. IPQA, Document Cell, Market Complaints, Market Recall, 00S, 00T, Process, Cleaning Validation, Review of BMR and BPR, Training ,QMS

To monitor routine GLP activities in lab, involves in planning and execution of GLP related activities like preparation of Calibration planner, Preventive Maintenance planner, Preparation and review of SOP, STP, AWR.