Vincit Labs PVT LTd

37 Job openings at Vincit Labs PVT LTd
Quality Controller pitampura, delhi, delhi 2 - 4 years INR 2.4 - 4.2 Lacs P.A. On-site Full Time

Sample Preparation and Analysis: Prepare samples for analysis using various techniques, such as extraction, digestion, filtration, and dilution. Perform analytical testing and characterization of samples using a wide range of analytical techniques and instrumentation, including HPLC, GC and UV-Vis, to determine chemical composition, identify impurities, and assess product quality. Data Interpretation and Reporting: Analyse the experimental data, interpret results, and draw conclusions based on statistical analysis, and quality control criteria to support analytical findings and troubleshoot analytical issues. Instrument Maintenance and Calibration: Maintain analytical instruments and equipment in proper working condition by performing routine maintenance, troubleshooting instrument malfunctions, and calibrating instruments according to manufacturer specifications to ensure data accuracy and instrument reliability. Evaluate instrument performance, monitor quality control parameters, and implement corrective actions as needed to address deviations, minimize variability, and maintain analytical accuracy and precision. Quality Assurance and Compliance: Ensure compliance with laboratory safety procedures, good laboratory practices (GLP). Participate in internal audits, proficiency testing, and quality assurance activities to assess laboratory performance, identify areas for improvement, and implement corrective and preventive actions to enhance operational efficiency and data quality. Experience: B.Sc or M.Sc with 2-4 years of industrial experience. Male candidate preffered NOTE: LOCATION IS OF CHANDIGARH, SONIPAT( BANAUR) Job Type: Full-time Pay: ₹20,000.00 - ₹35,000.00 per month Work Location: In person

Quality Controller pitampura 2 - 4 years INR 2.4 - 4.2 Lacs P.A. On-site Full Time

Sample Preparation and Analysis: Prepare samples for analysis using various techniques, such as extraction, digestion, filtration, and dilution. Perform analytical testing and characterization of samples using a wide range of analytical techniques and instrumentation, including HPLC, GC and UV-Vis, to determine chemical composition, identify impurities, and assess product quality. Data Interpretation and Reporting: Analyse the experimental data, interpret results, and draw conclusions based on statistical analysis, and quality control criteria to support analytical findings and troubleshoot analytical issues. Instrument Maintenance and Calibration: Maintain analytical instruments and equipment in proper working condition by performing routine maintenance, troubleshooting instrument malfunctions, and calibrating instruments according to manufacturer specifications to ensure data accuracy and instrument reliability. Evaluate instrument performance, monitor quality control parameters, and implement corrective actions as needed to address deviations, minimize variability, and maintain analytical accuracy and precision. Quality Assurance and Compliance: Ensure compliance with laboratory safety procedures, good laboratory practices (GLP). Participate in internal audits, proficiency testing, and quality assurance activities to assess laboratory performance, identify areas for improvement, and implement corrective and preventive actions to enhance operational efficiency and data quality. Experience: B.Sc or M.Sc with 2-4 years of industrial experience. Male candidate preffered NOTE: LOCATION IS OF CHANDIGARH, SONIPAT( BANAUR) Job Type: Full-time Pay: ₹20,000.00 - ₹35,000.00 per month Work Location: In person

R&D Chemist delhi, delhi 0 years INR 1.8 - 4.8 Lacs P.A. On-site Full Time

Conducting day- to-day Experiments. Monitoring of the experiments with observations. Calculation of moles & mole ratios. Calculation of molar yield. Familiar on properties of solvents, raw materials and catalysts like boiling point, melting point, density, freezing point etc Familiar on MSDS. Periodically checking the Lab instruments for their maintenance. The difficulties / problems arise during the experiment will be report to Seniors. Interaction with AR&D and stores departments for getting analysis results and raw materials in time. Maintenance of glassware and Equipment. Maintenance of lab clean and tidy cleaning and segregation of glassware. Storage of raw materials, intermediates and finished products based on compatibility. Scale-up and coordination with Production Chemists. Role: Research Associate / Engineer Industry Type: Pharmaceutical & Life Sciences Department: Research & Development Employment Type: Full Time, Permanent Role Category: Pharmaceutical & BiotechnologyEducation UG: B.Sc in Any Specialization PG: MS/M.Sc(Science) in Any SpecializationKey SkillsSkills highlighted with ‘‘ are preferred keyskillsResearch And DevelopmentProcess DevelopmentMaintenance OperationsFormulationCalculation Male candidate preffered Location- Sonipat Job Type: Full-time Pay: ₹15,000.00 - ₹40,000.00 per month Work Location: In person

Senior Quality Analyst delhi 0 years INR 3.30502 - 9.70682 Lacs P.A. On-site Full Time

* Leading and managing the QA team in the development, implementation, and execution of quality assurance processes and strategies. * Developing and enforcing quality standards and procedures, ensuring all team members follow them. * Monitoring and analysing key quality metrics to track product performance and identify areas for improvement. * Working closely with product development, engineering, and operations teams to ensure that quality standards are integrated into the product lifecycle. * Overseeing the planning and execution of audits, inspections, and tests to evaluate product quality. * Developing and maintaining quality documentation, including test plans, reports, and defect tracking records. * Establishing and maintaining a strong communication channel with other departments to ensure quality expectations are met throughout the production process. * Conducting root cause analysis of quality issues and implementing corrective actions to prevent recurrence. * Providing leadership, training, and development opportunities to QA staff to enhance team skills and performance. Your tasks * Oversee and coordinate the daily operations of the QA department, ensuring all activities align with business goals and customer requirements. * Lead the development and execution of quality assurance plans for products, including both manual and automated testing strategies. * Perform risk assessments and ensure quality risks are mitigated throughout the product life cycle. * Monitor testing progress, defect trends, and product performance, providing status updates to senior management. * Ensure compliance with regulatory standards, industry best practices, and company policies regarding quality assurance processes. * Collaborate with engineering, product management, and customer support teams to gather feedback and improve product quality. * Conduct periodic team performance reviews, offer constructive feedback, and implement continuous improvement initiatives. * Ensure all product releases meet defined quality criteria before they are launched to customers. * Assist in the identification and implementation of new tools and technologies to enhance the quality assurance processes. * Manage and mentor the QA team, fostering a collaborative and results-driven environment. * Stay updated on industry trends, new quality management methodologies, and regulatory changes that affect product quality. Location: Ganaur, Haryana MALE CANDIDATE PREFFERED Job Type: Full-time Pay: ₹330,501.64 - ₹970,682.43 per year Work Location: In person

R&D Chemist delhi 0 years INR 1.8 - 4.8 Lacs P.A. On-site Full Time

Conducting day- to-day Experiments. Monitoring of the experiments with observations. Calculation of moles & mole ratios. Calculation of molar yield. Familiar on properties of solvents, raw materials and catalysts like boiling point, melting point, density, freezing point etc Familiar on MSDS. Periodically checking the Lab instruments for their maintenance. The difficulties / problems arise during the experiment will be report to Seniors. Interaction with AR&D and stores departments for getting analysis results and raw materials in time. Maintenance of glassware and Equipment. Maintenance of lab clean and tidy cleaning and segregation of glassware. Storage of raw materials, intermediates and finished products based on compatibility. Scale-up and coordination with Production Chemists. Role: Research Associate / Engineer Industry Type: Pharmaceutical & Life Sciences Department: Research & Development Employment Type: Full Time, Permanent Role Category: Pharmaceutical & BiotechnologyEducation UG: B.Sc in Any Specialization PG: MS/M.Sc(Science) in Any SpecializationKey SkillsSkills highlighted with ‘‘ are preferred keyskillsResearch And DevelopmentProcess DevelopmentMaintenance OperationsFormulationCalculation Male candidate preffered Location- Sonipat Job Type: Full-time Pay: ₹15,000.00 - ₹40,000.00 per month Work Location: In person

Junior Quality Analyst delhi 0 years INR 3.6 - 5.4 Lacs P.A. On-site Full Time

* Leading and managing the QA team in the development, implementation, and execution of quality assurance processes and strategies. * Developing and enforcing quality standards and procedures, ensuring all team members follow them. * Monitoring and analysing key quality metrics to track product performance and identify areas for improvement. * Working closely with product development, engineering, and operations teams to ensure that quality standards are integrated into the product lifecycle. * Overseeing the planning and execution of audits, inspections, and tests to evaluate product quality. * Developing and maintaining quality documentation, including test plans, reports, and defect tracking records. * Establishing and maintaining a strong communication channel with other departments to ensure quality expectations are met throughout the production process. * Conducting root cause analysis of quality issues and implementing corrective actions to prevent recurrence. * Providing leadership, training, and development opportunities to QA staff to enhance team skills and performance. Your tasks * Oversee and coordinate the daily operations of the QA department, ensuring all activities align with business goals and customer requirements. * Lead the development and execution of quality assurance plans for products, including both manual and automated testing strategies. * Perform risk assessments and ensure quality risks are mitigated throughout the product life cycle. * Monitor testing progress, defect trends, and product performance, providing status updates to senior management. * Ensure compliance with regulatory standards, industry best practices, and company policies regarding quality assurance processes. * Collaborate with engineering, product management, and customer support teams to gather feedback and improve product quality. * Conduct periodic team performance reviews, offer constructive feedback, and implement continuous improvement initiatives. * Ensure all product releases meet defined quality criteria before they are launched to customers. * Assist in the identification and implementation of new tools and technologies to enhance the quality assurance processes. * Manage and mentor the QA team, fostering a collaborative and results-driven environment. MALE CANDIDATE PREFERED * Stay updated on industry trends, new quality management methodologies, and regulatory changes that affect product quality. Location: Ganaur, Haryana Job Type: Full-time Pay: ₹30,000.00 - ₹45,000.00 per month Work Location: In person

Regulatory Affairs Manager delhi 8 - 12 years INR 4.8 - 9.6 Lacs P.A. On-site Full Time

1. Strong knowledge of regulatory affairs principles, regulations, and guidelines, particularly in the relevant industry. 2. Maintain a thorough understanding of international regulations in relevant markets and guide the organization regarding international expansion plans. 3. Provide regulatory guidance and support to internal stakeholders, including product development teams, to ensure that regulatory requirements are incorporated into the development process. 4. Collaborate with cross-functional teams including R&D, Quality Assurance, and Legal to ensure that all regulatory requirements are met throughout the product lifecycle. 5. Prepare and submit regulatory submissions, including but not limited to, product registrations, pre-market notifications, and post-market surveillance reports. 6. Conduct risk assessments and develop mitigation strategies to manage regulatory risks. 7. Monitor and track regulatory compliance metrics and provide regular reports to senior management. 8. Maintain a thorough understanding of international regulations in relevant markets and guide the organization regarding international expansion plans. Regulatory Affairs Manager Required Skills & Experience 1. Strong knowledge of regulatory affairs principles, regulations, and guidelines, particularly in the relevant industry. 2. Excellent understanding of the product development process and the ability to apply regulatory requirements to each stage. 3. Exceptional attention to detail and ability to review and interpret technical documentation, scientific data, and regulatory guidelines accurately. 4. Excellent written and verbal communication skills, with the ability to effectively communicate complex regulatory concepts to both technical and non-technical stakeholders. 5. Strong project management skills and the ability to prioritize and manage multiple projects simultaneously. 6. Proficient in using regulatory databases and software applications to track and manage regulatory submissions and documents. 7. Strong analytical and problem-solving skills, with the ability to identify and resolve regulatory issues effectively. 8. Demonstrated ability to work collaboratively in cross-functional teams and effectively influence stakeholders at all levels. 9. Experience in interacting with regulatory authorities and managing regulatory inspections and audits. 10. Experience in developing and maintaining regulatory compliance documentation, including technical files, regulatory dossiers, and other relevant documentation. Educational Qualification B. Pharm with 8-12 years of experience in API regulatory affairs M. Pharm with 5-8 years of experience in API regulatory affairs Job Type: Full-time Pay: ₹40,000.00 - ₹80,000.00 per month Work Location: In person

Quality Analyst gurgaon 10 - 15 years INR 8.4 - 14.4 Lacs P.A. On-site Full Time

Quality Analyst - Head Team Leadership: Lead, mentor, and develop the QA team through training and performance reviews. Quality Management System (QMS): Establish and maintain a robust quality system, including SOPs, quality manuals, and other necessary documentation. Audits and Compliance: Conduct internal audits and prepare the site for external regulatory and customer audits. Ensure all activities adhere to GMP, GLP, and ISO guidelines. Documentation Review: Review and approve key documents, including batch manufacturing records (BMRs), batch packaging records (BPRs), specifications, Technical package, Stability protocol and validation documents etc. Review of drug substances as per compendial norms. Product Lifecycle Management: Oversee the release of drug substance, intermediates, and raw materials. Manage the investigation of deviations, out-of-specification (OOS) & out of trend (OOT) results, and market complaints, and ensure timely implementation of corrective and preventive actions (CAPA). Change Control: Manage the change control process to ensure that changes are properly evaluated, documented, and approved. Supplier Qualification: Oversee the qualification of raw material suppliers to ensure their compliance and the quality of incoming materials. Continuous Improvement: Drive continuous improvement initiatives within the quality department and across the organization. Qualifications and skills •* *Education: Typically requires a Bachelor's or Master's degree in Pharmacy (B.Pharm, M.Pharm) or Chemistry (B.Sc, M.Sc). •* *Experience: 10-15 years of experience in a pharmaceutical QA or QC role, specifically within API or bulk drug manufacturing, is necessary. •* *Technical Skills: Proficiency in quality management systems, GMP, validation, and a strong understanding of regulatory requirements is essential. Job Type: Full-time Pay: ₹70,000.00 - ₹120,000.00 per month Work Location: In person

Production Chemist delhi, delhi 4 - 6 years INR 3.0 - 6.0 Lacs P.A. On-site Full Time

Role & responsibilities Train on, comply with, and understand all policy and procedures at Experic including Regulatory, Safety, SOPs, Work Instructions, etc. Assist in the development of new processes in procedures under the management direction including: Becoming subject matter expert for pharmaceutical manufacturing equipment. Adapting understanding of equipment into (write) new SOPs and work instructions and assisting in the training of additional staff on equipment specialty. Front line troubleshooting of processes and equipment. Perform Pharmaceutical Manufacturing activities including: Batch Documentation/Record Generation Materials sampling, staging, dispensing, and return Pharmaceutical Equipment and Room set-up, operation, and cleaning Use of appropriate personal safety equipment and engineering controls In-process inspection and sampling Perform developmental manufacturing experiments under the direction of Production head/Supervisor. Support investigational and quality systems activities. Assist maintenance in the performance of preventative maintenance activities, troubleshooting and repair of equipment. Participate in continuous improvement activities at Experic. Carries out duties in compliance with all federal and state regulations and guidelines. Complies with all company and site policies and procedures. Minimum qualification : 10th Pass with 4-6 years of experience in Bulk drug/chemical plant. Job Type: Full-time Pay: ₹25,000.00 - ₹50,000.00 per month Work Location: In person

Production Chemist delhi 4 - 6 years INR 3.0 - 6.0 Lacs P.A. On-site Full Time

Role & responsibilities Train on, comply with, and understand all policy and procedures at Experic including Regulatory, Safety, SOPs, Work Instructions, etc. Assist in the development of new processes in procedures under the management direction including: Becoming subject matter expert for pharmaceutical manufacturing equipment. Adapting understanding of equipment into (write) new SOPs and work instructions and assisting in the training of additional staff on equipment specialty. Front line troubleshooting of processes and equipment. Perform Pharmaceutical Manufacturing activities including: Batch Documentation/Record Generation Materials sampling, staging, dispensing, and return Pharmaceutical Equipment and Room set-up, operation, and cleaning Use of appropriate personal safety equipment and engineering controls In-process inspection and sampling Perform developmental manufacturing experiments under the direction of Production head/Supervisor. Support investigational and quality systems activities. Assist maintenance in the performance of preventative maintenance activities, troubleshooting and repair of equipment. Participate in continuous improvement activities at Experic. Carries out duties in compliance with all federal and state regulations and guidelines. Complies with all company and site policies and procedures. Minimum qualification : 10th Pass with 4-6 years of experience in Bulk drug/chemical plant. Job Type: Full-time Pay: ₹25,000.00 - ₹50,000.00 per month Work Location: In person

Dispatch Executive delhi 0 years INR Not disclosed On-site Full Time

Dispatch Planning & Execution Develop and execute daily/weekly/ monthly dispatch schedules based on customer orders, production plans, and inventory levels. Ensure timely availability of packing materials, approved finished goods, and required documentation. Monitor and manage dispatch timelines for domestic and export shipments. B. Documentation & Compliance Ensure accurate preparation and review of dispatch-related documents: COA (Certificate of Analysis) MSDS / SDS Packing List Commercial Invoice Batch Release Note Gate Pass/Delivery Challan Export documentation (LC documents, customs papers, AWB/BL, etc.) Ensure compliance with GDP, cGMP, FDA, ICH, and regulatory requirements . C. Coordination & Communication Liaise with QA/QC, Warehouse, Production, Regulatory Affairs, and Customer Service for dispatch readiness. Coordinate with freight forwarders, transporters, CHA (Custom House Agents), and courier agencies. Communicate with domestic & international customers regarding dispatch status, delivery timelines, and shipment documents. D. Inventory & Warehouse Management Monitor FG (Finished Goods) inventory to align dispatch and delivery commitments. Oversee storage compliance for APIs (temperature, humidity, segregation). Ensure proper FIFO/FEFO adherence and batch traceability. E. Audits & Quality Systems Participate in internal, external, customer, and regulatory audits. Maintain dispatch SOPs and ensure team adherence. Conduct deviations, CAPAs, RCA (Root Cause Analysis) for dispatch-related issues. F. Logistics Optimization Optimize transportation routes, freight costs, and carrier performance. Evaluate transporters and logistics service providers periodically. Monitor OTIF (On-Time In-Full) metrics and drive continuous improvement. 3. Skills & Competencies Strong understanding of cGMP / GDP guidelines and API handling regulations. Knowledge of export-import documentation, DG shipments, customs processes . SAP / ERP / WMS proficiency. Excellent leadership, communication, and cross-functional coordination skills. Analytical approach to solve logistical issues under time pressure. 4. Qualifications & Experience Education: B.Sc / B.Pharm / M.Sc / MBA in Supply Chain or related discipline. Experience: in dispatch/logistics within API or pharmaceutical manufacturing . Experience in handling domestic & international shipments is mandatory. Knowledge of IATA rules for hazardous chemicals (if applicable). Location is Punjab candidate should be immidiate joiner and must be comforatble with location. Senior Manager Job Type: Full-time Pay: ₹20,000.00 - ₹150,000.00 per month Work Location: In person

Shift Operator delhi, delhi 2 - 3 years INR 2.4 - 4.8 Lacs P.A. On-site Full Time

1. Inventory & Material Management Maintain accurate records of RM, PM, consumables, and engineering spares. Ensure timely receipt, storage, and issuance of materials as per SOP. Monitor stock levels and initiate purchase requests to avoid shortages. Conduct daily, weekly, and monthly stock reconciliation. Implement FEFO/FIFO for all materials. 2. Compliance & Documentation Maintain all store records as per GMP/GDP and audit requirements . Ensure proper labeling, identification, and documentation of materials. Prepare GRN (Goods Receipt Note), Issue Slips, Stock Registers, and Material Movement reports. Support internal, external, and regulatory audits. 3. Storage & Handling Ensure proper storage conditions for sensitive raw materials (temperature, humidity, segregation). Monitor and maintain cleanliness, pest control, and safety standards in the store area. Ensure compliance with EHS (Environment, Health & Safety) guidelines. 4. Coordination Coordinate with Purchase, Production, QC, QA, and Finance teams for smooth operations. Follow up with vendors for timely delivery based on requirements. Support production planning by ensuring timely availability of materials. 5. System & Process Management Manage ERP/Inventory Management System for all material entries. Ensure correct posting of inward and outward material transactions. Improve store processes and implement best practices for efficiency. 6. Team Management Lead and supervise store staff and helpers. Assign tasks, monitor performance, and ensure proper training on SOPs. Male CANDIDATE PREFFERED LOCATION SONIPAT BACKGROUND MUST BE FROM PHARMACEUTICAL COMPANY EXPERIEINCE- 2-3 YEARS Job Type: Full-time Pay: ₹20,000.00 - ₹40,000.00 per month Work Location: In person

Production Operator delhi, delhi 3 - 4 years INR 2.4 - 4.8 Lacs P.A. On-site Full Time

Train on, comply with, and understand all policy and procedures at Experic including Regulatory, Safety, SOPs, Work Instructions, etc. Assist in the development of new processes in procedures under the management direction including: Becoming subject matter expert for pharmaceutical manufacturing equipment. Adapting understanding of equipment into (write) new SOPs and work instructions and assisting in the training of additional staff on equipment specialty. Front line troubleshooting of processes and equipment. Perform Pharmaceutical Manufacturing activities including: Batch Documentation/Record Generation Materials sampling, staging, dispensing, and return Pharmaceutical Equipment and Room set-up, operation, and cleaning Use of appropriate personal safety equipment and engineering controls In-process inspection and sampling Perform developmental manufacturing experiments under the direction of Production head/Supervisor. Support investigational and quality systems activities. Assist maintenance in the performance of preventative maintenance activities, troubleshooting and repair of equipment. Participate in continuous improvement activities at Experic. Carries out duties in compliance with all federal and state regulations and guidelines. Complies with all company and site policies and procedures. Candidate must be having 3-4 years of experience Male candidate preffered location - sonipat must be near about location Job Type: Full-time Pay: ₹20,000.00 - ₹40,000.00 per month Work Location: In person

Human Resource Executive delhi 0 years INR 2.4 - 3.6 Lacs P.A. On-site Full Time

Responsibilities: * Manage recruitment process from sourcing to onboarding * Collaborate with hiring managers on talent acquisition strategies * Ensure compliance with HR policies and procedures MALE CANDIDATE LOCATION- PUNJAB CANDIDATE SHOULD BE NEAR BY THAT LOCATION Job Type: Full-time Pay: ₹20,000.00 - ₹30,000.00 per month Work Location: In person

Production Operator delhi 3 - 4 years INR 2.4 - 4.8 Lacs P.A. On-site Full Time

Train on, comply with, and understand all policy and procedures at Experic including Regulatory, Safety, SOPs, Work Instructions, etc. Assist in the development of new processes in procedures under the management direction including: Becoming subject matter expert for pharmaceutical manufacturing equipment. Adapting understanding of equipment into (write) new SOPs and work instructions and assisting in the training of additional staff on equipment specialty. Front line troubleshooting of processes and equipment. Perform Pharmaceutical Manufacturing activities including: Batch Documentation/Record Generation Materials sampling, staging, dispensing, and return Pharmaceutical Equipment and Room set-up, operation, and cleaning Use of appropriate personal safety equipment and engineering controls In-process inspection and sampling Perform developmental manufacturing experiments under the direction of Production head/Supervisor. Support investigational and quality systems activities. Assist maintenance in the performance of preventative maintenance activities, troubleshooting and repair of equipment. Participate in continuous improvement activities at Experic. Carries out duties in compliance with all federal and state regulations and guidelines. Complies with all company and site policies and procedures. Candidate must be having 3-4 years of experience Male candidate preffered location - sonipat must be near about location Job Type: Full-time Pay: ₹20,000.00 - ₹40,000.00 per month Work Location: In person

Shift Operator delhi 2 - 3 years INR 2.4 - 4.8 Lacs P.A. On-site Full Time

1. Inventory & Material Management Maintain accurate records of RM, PM, consumables, and engineering spares. Ensure timely receipt, storage, and issuance of materials as per SOP. Monitor stock levels and initiate purchase requests to avoid shortages. Conduct daily, weekly, and monthly stock reconciliation. Implement FEFO/FIFO for all materials. 2. Compliance & Documentation Maintain all store records as per GMP/GDP and audit requirements . Ensure proper labeling, identification, and documentation of materials. Prepare GRN (Goods Receipt Note), Issue Slips, Stock Registers, and Material Movement reports. Support internal, external, and regulatory audits. 3. Storage & Handling Ensure proper storage conditions for sensitive raw materials (temperature, humidity, segregation). Monitor and maintain cleanliness, pest control, and safety standards in the store area. Ensure compliance with EHS (Environment, Health & Safety) guidelines. 4. Coordination Coordinate with Purchase, Production, QC, QA, and Finance teams for smooth operations. Follow up with vendors for timely delivery based on requirements. Support production planning by ensuring timely availability of materials. 5. System & Process Management Manage ERP/Inventory Management System for all material entries. Ensure correct posting of inward and outward material transactions. Improve store processes and implement best practices for efficiency. 6. Team Management Lead and supervise store staff and helpers. Assign tasks, monitor performance, and ensure proper training on SOPs. Male CANDIDATE PREFFERED LOCATION SONIPAT BACKGROUND MUST BE FROM PHARMACEUTICAL COMPANY EXPERIEINCE- 2-3 YEARS Job Type: Full-time Pay: ₹20,000.00 - ₹40,000.00 per month Work Location: In person

CRM Executive delhi, delhi 0 years INR 1.8 - 3.6 Lacs P.A. On-site Full Time

Manage backend office operations and maintain accurate records. Share dispatch details with customers and address related queries. Follow up with clients for pending payments in a professional manner. Female candidate required Job Type: Full-time Pay: ₹15,000.00 - ₹30,000.00 per month Work Location: In person

CRM Executive delhi 0 years INR 1.8 - 3.6 Lacs P.A. On-site Full Time

Manage backend office operations and maintain accurate records. Share dispatch details with customers and address related queries. Follow up with clients for pending payments in a professional manner. Female candidate required Job Type: Full-time Pay: ₹15,000.00 - ₹30,000.00 per month Work Location: In person

Store Operator sonipat, haryana 1 years INR 1.8 - 3.0 Lacs P.A. On-site Full Time

Operate computer systems and POS (Point of Sale) machines for accurate billing. Generate customer bills, invoices, and receipts. Handle cash, card, UPI, and other digital payment modes responsibly. Maintain daily billing records and reconcile cash and digital transactions. Assist customers during billing and resolve basic billing-related queries. Ensure correct pricing, discounts, offers, and tax (GST) application. Maintain cleanliness and organization of the billing counter area. Coordinate with floor staff and store in-charge for smooth operations. Report discrepancies or system issues to the supervisor immediately. Follow company policies and billing procedures strictly. CANDIDATE MALE PREFFERED LOCATION GANAUR HARYANA EXPERIENCE- 6MONTH- 1 YEAR Job Type: Full-time Pay: ₹15,000.00 - ₹25,000.00 per month Work Location: In person

Store Operator sonipat 1 years INR 1.8 - 3.0 Lacs P.A. On-site Full Time

Operate computer systems and POS (Point of Sale) machines for accurate billing. Generate customer bills, invoices, and receipts. Handle cash, card, UPI, and other digital payment modes responsibly. Maintain daily billing records and reconcile cash and digital transactions. Assist customers during billing and resolve basic billing-related queries. Ensure correct pricing, discounts, offers, and tax (GST) application. Maintain cleanliness and organization of the billing counter area. Coordinate with floor staff and store in-charge for smooth operations. Report discrepancies or system issues to the supervisor immediately. Follow company policies and billing procedures strictly. CANDIDATE MALE PREFFERED LOCATION GANAUR HARYANA EXPERIENCE- 6MONTH- 1 YEAR Job Type: Full-time Pay: ₹15,000.00 - ₹25,000.00 per month Work Location: In person