Devraj Jatav Email & Phone Number

Kolkata, Wb, In

Ahmedabad, Gujarat, India

Kolkata, West Bengal, India

 Deployment and monitoring of Quality management and compliance program (CQA Guideline, policies, and, protocols) to drive Quality @ manufacturing sites and supply chain (Including CFA and distributors) of Health care and HPC business category.  New 3P (Contract Manufacturing) development (Training and Development of QMS, Audit and compliance management) To handle Vendor selection audit, qualification, and vendor approval. Vendor performance monitoring and rating. GMP compliance audit at all manufacturing sites (including contract manufacturing sites) producing CCD and HCD products and GSP compliance review all 26 depots/CFA and E-commerce warehouses To lead and manage the Consumer/Customer care cell of the company to handle their grievance, feedback, and complaints and provide resolution by leading complaint investigation, RCA and CAPA, and sample replacement. To extend support to the site QA team in different external (Customer) audits GMP certifications and accreditations. Quality review with a cross-functional team, MIS reporting to leadership on key Quality performance indicators such as Change Management, Deviations/OOS Management, Consumer/ Customer Complaints, Quality Incidents, QIP, and Vendor performance and Audits).

Kolkata, West Bengal, India

 Innovation Quality Excellence for all NPD projects & and New product rollout and ensure FTR at minimum risk level. Product quality performance in the logistics and at the point of sale. Standardization and deployment of product and pack Quality standards and product quality defect matrix. Validate and monitor AQL at all manufacturing sites. Technical document review and issuance to the sites (product and packing specifications, formulation, and technical specifications)  Site capability gap analysis for successful technology transfer of roll-out products, Hardware compliance (Manufacturing, filling & packing) verification at the site, Equipment Qualification, and process validation at all sites.

Silvassa

 Deployment of QMS, policies, and guidelines and to lead and mentor quality and Manufacturing team for seamless function and First-time right Quality Products Transposition of Customer technical dockets into internal processes, Master validation plan, validation protocols & reports, Equipment qualification, and report. Process validation etc. Management review and QMS compliance audit  New product rollouts, Annual Product Reviews, protocols, Handling customer complaints, Investigations, RCA and CAPA management, Internal Audits, 3P labs, Vendor Audits etc.

Kolkata

Key Accountabilities Overall responsibility for Quality Management at 3P (contract Manufacturing) sites and compliance audits GMP compliance Audits @ Emami's own manufacturing site producing HPC products, Healthcare products Ayurveda Medicines. Product technology transfer - (Site to site) and product rollout at manufacturing sites R&D QA – Product technology documentation and compliance review (Product Formulations, technical specifications, FDA approval documents, etc.) and transfer to the site. Manufacturing Excellence, training, and Quality capability improvement at the site. Annual product quality review.

Mumbai, Maharashtra, India

Key Accountabilities as R&D Executive To draft various trial protocols for consumer claim studies, clinical efficacy trials, and review take approval from the ethical committee. Claim Benchmarking study - liaising with CRA and various research agencies to carry out sensorial, clinical, and claim support studies in-house as well as outsourced. To set up, train, and quality sensory panels (QDA panel, cord panel) to carry out various in-house claim support studies of Indian and global market projects of Oral Care products. To support the legal and regulatory team in case of any query or defend any legal or regulatory notices on product claims.Key Accountabilities as QA Executive (July 2007 - June 2009) To ensure smooth day-to-day functioning of QC and microbiology lab,  To lead TPM edge Quality pillar and compliance audit and product HAPPC study and compliance monitoring. Supplier Quality performance and audit Management (under the direction of CQA) Site internal audit, 3P Contract manufacturing, and co-packers Audit management Cleaning and sanitization validation of product manufacturing, filling, and packing equipment of OTC & non-OTC products. Responsible for Validation Master plan and compliance of USFDA plant facility, Equipment and instruments qualification, water system validation, cleaning and sanitization validation of OTC product manufacturing, filling, and packing equipment

Silvassa

Key Accountabilities Responsible for smooth operation & compliance of QC laboratory (sampling, testing, and product release documentation), Monitoring of DPMO (Online and terminal inspection) trend of all the products manufactured at Site.  Plant hygiene, smooth operation & compliance of ETP and DM Water Plant.  Quality Documentation & management of FDA-related matters, FDA application preparation (based on documents and technical documents received from R&D and Packaging development team).  Handling SAP quality module, Preparation BPR, BMR in SAP, SOP preparation, training, and implementation.

Master Of Science (Ms), Microbiology, General

Qualified in CSIR NET

Green Belt Certification Course, Lean Six Sigma

Activities and Societies: Lean Six Sigma Green Belt

Master Of Business Administration (Mba), Operations Management And Supervision

Activities and Societies: MBA in Operations Managemenet MBA in Operation Mangement