ASHA GARKOTI

• Responsible for Change/Updating of SOPs as per cGMP practices.
• Responsible for internal Audit planning and execution as per SOP.
• Data Analysis of 1st Release / Hold / Rework / Rejected Production as per value on daily & monthly basis.
• Ensure Quality Control & Quality assurance Activities of personal care & Cosmetic products.
• Ensure Quality & Regulatory Compliances for Finished Products.
• Implementation of Changes in regulatory requirements.
• Troubleshooting with CAPA for quality improvements.
• Handling of Market Complains.
• Root Cause Analysis & implementation of Corrective & Preventive Actions.
• Responsible for Self Inspection Procedure & Internal Audit of all Departments.
• Conduct Training to Shop floor employees to derive the Quality managements System.
• Monthly Quality Reports, NCs-reports, CAPA reports.
• Customer Complaints Investigation reports.
• Preparation, Approval & Review of SOPs.
• Finished Goods Audits before dispatches.
• Quality Management System & Site Master File Preparation & updation
• Hygiene: Plant & Personnel
• Good Documentation Practices, Incident & Deviations / Nonconformities, Product Recall handling.
• Change Control & implementation, Internal Audits & Closure and Management Review
• Trainings & Development, GMP Implementation & Compliance
• Standard Testing Procedure, Standard Testing Specification, OOS, OOT & Laboratory Investigation
• Material: Inspection, Sampling, Testing, Storage & Release.
• Plan and execute trials of new product development in coordination with the R&D and Supply Chain team.
• Identify Quality Control Points and Critical Control Points for Bulk manufacturing processes.
• Ensure Product stability Studies and Packaging compatibility Studies being done timely.

• Create and update MSDS for all FG batches as per requirement of Domestic and Export regions.
• Label Artwork gets checked and approved as per the checklist.
• Constantly strive to improve GLP, GMP, and QMS practices at the Plant.
• Experience about FDA Ayurveda, and Legal Metrology Act.
• Skilled in managing the overall technical & managerial aspects and handling planning for better productivity.
• Overseeing the production activities by ensuring the targets achieved and compliance with the cGMP and follow safety regulations.
• Adroit in managing the performance of the production team to make sure that the department is operating efficiently.
• Planning for day-to-day production and Quality related activities, allocating work for achieving daily, weekly, and monthly targets.
• To review and improve documents as per the need from time to time.
• To follow through on set processes and ensure adherence to good manufacturing practices (GMP), Safe Quality Product (SQP) standards.
• Handling, review, and investigation of Market Complaints implement corrective actions.
• To carry out internal audits to establish and maintain uniform and controlled methods for planning, scheduling, and coordination performing and reporting.
• Ensuring that the manufactured products are inspected at all stages as per the norms.
• Expertise in managing operations with focus on profitability by ensuring optimal utilization of resources.
• To determine and document any areas that may need improvement.
• To arrange necessary trainings & assessments of all personnel.
• Documentation as per ISO & cGMP's norms
• Inspecting the entire manufacturing and filling/Packing process & implementation of Quality Norms.
• Follow-up with Supply Chain regarding Quality Issues of incoming RM & PM.
• Control Sample Management of Raw materials & Finished Goods & Stability Studies.
• Preparation, Approval & Review of SOPs.
• Co-ordination with R&D regarding new formulations & implementation of new Developments
• Ensure Sampling, Analysis, Approvals & Timely Releasing of RM/PM/Intermediates & FGs.
• Ensure IPQC Activities during manufacturing & packaging processes.
• Calibration & Validation
• Maintain Stability of all New R&D Trial Products as per SOP with Data.
• Real-time study of 3P products as per SOP.
• Maintain Stability of all 3P Products as per SOP with Data.
• Chemical testing of homeopathic medicine like alcohol Percentage by distillation of syrup, and Disintegration time, Lactose content, Friability, Hardness of tablet.

• Search and analyze the latest products from Indian International e-commerce websites.
• Compare prices products listing from competitive websites.
• Technical aptitude and ability to learn web-based tools.
• Experience in launching of Skin Care, Hair Care, and Body Care & Color Cosmetic product range.
• Vendor development & Negotiation - from Raw Material to Packaging to Finished Goods.
• Benchmarking of key competitors & Trend Analysis.
• Leadership: Full ownership of entire Project Deliverables
• Briefing the internal R&D functions and ensuring high quality Innovation & Creativity with strict adherence to timeline.
• To work closely with the procurement team to identify new sources of supply of product needs and sources new packaging Material and passes information on new ideas to NPD Department.
• Trials for New Product Development like Shampoo, Hand wash, Hair cream & Oil.
• Audit Manufacturing Units, Vendors & Finalization.
• Vendor Development (RM & PM).
• Costing Approvals & Testing Parameters Observations.
• Involvement in Artwork preparation & coordination with Graphics & Content writer team.
• Certification, Product Approval, Claims Analysis.
• Samples Trials (Physical Parameters (QC), Results).
• Final Costing Approvals in house & PO/PI.
• Invoices Payment processing & coordination with finance team.
• Day to day follow ups of order processing till production.
• Material collection from vendors (Sampling).
• Material Collection (Sampling) as per requirement & Vendor interaction.
• In house stability check of every product (R&D Trial Batch).
• Maintaining complete documentation of all existing and new products.
• Vendor factory visit for QA and pilot batches.
• New Vendor development for quality optimization.

• Designed and setup of microbiology lab according to regulatory requirements.
• Validated new equipment's, media, and glassware & laboratory consumables for microbiology lab.
• Ensured all testing is performed according to regulatory methods and policy and adheres to good microbiological practices.
• This includes the set up and administration of a laboratory quality assurance system that covers method and material qualification as well as equipment IQ/OQ/PQ, calibration & maintenance.
• Developed & implemented a microbiological sampling and testing program for water, raw materials, work-in-process (WIP), environmental samples & finished products at the facility.
• Developed and implemented plant floor micro control programs based on the C&S Standard, Control Point Monitoring.
• FG/RM MIR Handling.
• Maintenance and preservation of microbial culture as per SOP & record maintenance.
• Preparing, Trend Analysis Reports of Microbiological Monitoring and MLTs of Purified, potable Water.
• Responsible that all Raw Material, Finished Product are analyzed as per specification and method of analysis provided by our Principal, IP, HPI.

• Colgate Palmolive Ltd
• Dabur India Ltd
• ITC Ltd.
• Godrej Consumers Ltd.
• Marico Ltd
• Kama Ayurveda Ltd
• Bajaj Corp. Ltd
• Ustara Ltd
• Wipro Ltd
• Future Consumer Ltd.
• Emami
• Hindustan Unilever Ltd.
• St. Botanica
• Sirona
• Praush
• My Glamm

5,80,000, 48,940

Current CTC + 40% hike (Negotiable)

• Knowledge of Excel, MSWord
• ERP
• LIMPS
• SAP

• Religion: Hindu
• Father's Name: Mr. Khimanand Garkoti
• Date of Birth: 07/01/91
• Gender: Male
• Nationality: Indian
• Marital Status: Married

Hindi & English