Swaroop Ladiya

Technical Supervisor, Formulation Manufacturing Facility (Tablet and Capsule) @Cadila Pharmaceuticals Limited

Jammu, IN

Current Technical Responsibilities:Day to Day Production Planning, coordination & control of respective production resources to effectively achieve the set production targets & quality standards.Allocation & work distribution of Operators & temporary man-powers.To conduct job training to subordinates on departmental procedures/SOPs.To monitor cCMP on shop floor.Verification of raw materials.To independently analyze in-process checks of formulations (Tablets, Capsules).To do Online Documentation (i.e. online filling of BMR, BPR & equipment log cards) with zero error and as per the Good Documentation Practices.Preparation & Review of BMR & BPR.Preparation & Review of SOPs.Involved in the various validations activities like:Review of protocols for qualification and validation of facility/equipment/product/process.Review of validation reports after execution of validation of facility/equipment/process.Assuring quality of products by:Ensuring SOP compliance, Performing internal quality audits, Controlling the changes made to facility/equipment/product/process & master documents by following change control procedure.Ensuring implementation of Corrective actions/Preventive actions proposed in Deviation/Failure investigations and Customer complaints.Coordination with QA/QC, SCM, Warehouse and Engg. for effective achievement of production target with optimum utilization of hands /materials/ machineries.To coordinate with Engg. dept. for scheduling of preventive maintenance. coordinate with QA & R&D/Technical services dept. for timely release of batches, IPQC tests, validation of processes, equipments as required for execution and submission of validation batches.Involved in the scale up implementation of mfg. process in the plant, Increased the Yield & quality of the product.Waste management – waste minimization.Undertaking process & cleaning validation including optimizing the cost, yields and quality to meet the regulatory requirements.

Jamia Hamdard-Hamdard University, India

PG Diploma in Pharmaceutical Regulatory Affairs (PGDPRA)

Doctor Harisingh Gour Central University, India

Master of Pharmacy (M.Pharm.)

H.C.Jain Higher Secondary School, Sagar

HSC (Phsics, Chemistry, Biology)

Doctor Harisingh Gour Vishwavidyalaya, India

Bachelor of Pharmacy (B.Pharm.)