Position Overview: The QA Chemist is responsible for ensuring that all manufacturing activities, documentation, and quality processes comply with Indian regulatory requirements (Schedule M, CDSCO, WHO-GMP, cGMP) . The role involves reviewing batch records, managing deviations, overseeing in-process controls, and ensuring data integrity and compliance throughout the manufacturing operations. Key Responsibilities:1. Batch Documentation & Quality Compliance Review Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR) for completeness, accuracy, and compliance with SOPs. Ensure all documents follow GDP (Good Documentation Practices) and ALCOA+ principles. Coordinate for batch release by verifying QC results, in-process checks, and production compliance. 2. In-Process Quality Assurance (IPQA) Carry out line clearance for dispensing, manufacturing, filling, and packaging operations. Conduct in-process checks such as weight variation, hardness, disintegration, leak test, pH, labeling checks , etc. Monitor adherence to approved procedures and ensure compliance with cGMP & Schedule M guidelines. 3. Quality Systems Management Handle and update Change Controls, Deviations, CAPA, Incidents, and Market Complaints . Maintain and revise SOPs, BMRs, and BPRs as per regulatory and operational requirements. Participate in internal audits and support external audits (State FDA, CDSCO, WHO, client audits). Ensure proper document archival and control through Document Control Systems. 4. Validation & Qualification Activities Assist in process validation, cleaning validation, equipment qualification , and hold-time studies. Review protocols and reports prepared as per WHO-GMP & ICH guidelines. 5. Training & Compliance Monitoring Conduct and document GMP, hygiene, and documentation training for production and support staff. Monitor shop floor practices to ensure adherence to hygiene, safety, and regulatory standards. Support investigation of OOS/OOT, deviations, and ensure timely implementation of CAPA. 6. Coordination & Cross-Functional Support Liaise with Production, QC, Warehouse, and Engineering for smooth quality operations. Ensure proper sampling of RM/PM and timely coordination with QC for testing. Verify dispensing activities and ensure correct material status labeling across the plant. Skills & Competencies Required: Strong understanding of GMP, WHO-GMP, and Schedule M requirements. Good knowledge of QA processes, documentation, and pharmaceutical manufacturing operations. Excellent attention to detail and compliance-oriented mindset. Strong communication skills and ability to enforce quality standards on the shop floor. Ability to handle audits and regulatory inspections. Qualification & Experience: Education: B.Sc / M.Sc in Chemistry, Pharmaceutical Chemistry, Microbiology, or related field. Experience: 1–5 years in QA department of a WHO-GMP certified pharmaceutical or nutraceutical plant. Freshers with good academic knowledge may also be considered. Job Types: Full-time, Permanent Pay: ₹18,000.00 - ₹30,000.00 per month Benefits: Paid sick time Paid time off Provident Fund Work Location: In person
Position Overview: The QA Chemist is responsible for ensuring that all manufacturing activities, documentation, and quality processes comply with Indian regulatory requirements (Schedule M, CDSCO, WHO-GMP, cGMP) . The role involves reviewing batch records, managing deviations, overseeing in-process controls, and ensuring data integrity and compliance throughout the manufacturing operations. Key Responsibilities:1. Batch Documentation & Quality Compliance Review Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR) for completeness, accuracy, and compliance with SOPs. Ensure all documents follow GDP (Good Documentation Practices) and ALCOA+ principles. Coordinate for batch release by verifying QC results, in-process checks, and production compliance. 2. In-Process Quality Assurance (IPQA) Carry out line clearance for dispensing, manufacturing, filling, and packaging operations. Conduct in-process checks such as weight variation, hardness, disintegration, leak test, pH, labeling checks , etc. Monitor adherence to approved procedures and ensure compliance with cGMP & Schedule M guidelines. 3. Quality Systems Management Handle and update Change Controls, Deviations, CAPA, Incidents, and Market Complaints . Maintain and revise SOPs, BMRs, and BPRs as per regulatory and operational requirements. Participate in internal audits and support external audits (State FDA, CDSCO, WHO, client audits). Ensure proper document archival and control through Document Control Systems. 4. Validation & Qualification Activities Assist in process validation, cleaning validation, equipment qualification , and hold-time studies. Review protocols and reports prepared as per WHO-GMP & ICH guidelines. 5. Training & Compliance Monitoring Conduct and document GMP, hygiene, and documentation training for production and support staff. Monitor shop floor practices to ensure adherence to hygiene, safety, and regulatory standards. Support investigation of OOS/OOT, deviations, and ensure timely implementation of CAPA. 6. Coordination & Cross-Functional Support Liaise with Production, QC, Warehouse, and Engineering for smooth quality operations. Ensure proper sampling of RM/PM and timely coordination with QC for testing. Verify dispensing activities and ensure correct material status labeling across the plant. Skills & Competencies Required: Strong understanding of GMP, WHO-GMP, and Schedule M requirements. Good knowledge of QA processes, documentation, and pharmaceutical manufacturing operations. Excellent attention to detail and compliance-oriented mindset. Strong communication skills and ability to enforce quality standards on the shop floor. Ability to handle audits and regulatory inspections. Qualification & Experience: Education: B.Sc / M.Sc in Chemistry, Pharmaceutical Chemistry, Microbiology, or related field. Experience: 1–5 years in QA department of a WHO-GMP certified pharmaceutical or nutraceutical plant. Freshers with good academic knowledge may also be considered. Job Types: Full-time, Permanent Pay: ₹18,000.00 - ₹30,000.00 per month Benefits: Paid sick time Paid time off Provident Fund Work Location: In person
Position Overview: The QC Chemist is responsible for carrying out analytical testing of raw materials, intermediates, finished formulations, purified water, and stability samples in compliance with Indian regulatory guidelines , including WHO-GMP, cGMP, GLP, and Schedule M . The incumbent ensures that all testing activities meet quality standards required by CDSCO and applicable pharmacopoeias (IP/USP/BP/EP). Key Responsibilities:1. Analytical Testing (As per Indian Pharma Standards) Perform analysis of raw materials, intermediates, and finished products as per Indian Pharmacopoeia (IP) and other approved methods. Test stability batches following ICH & CDSCO stability requirements . Conduct instrument-based analysis using HPLC, GC, UV-Vis spectrophotometer, FTIR, Dissolution Apparatus, pH meter, KF titrator, etc. Carry out Water Testing (Purified Water & WFI) as per IP limits and Schedule M requirements . Ensure timely sampling and testing in coordination with Production, QA, and Warehouse. 2. Documentation & Regulatory Compliance Maintain test records as per GDP (Good Documentation Practice) guidelines mandated by CDSCO. Prepare COA, test reports, logbooks, and maintain analytical raw data in compliance with Audit Trail requirements . Ensure all testing is in line with WHO-GMP & Schedule M guidelines applicable in India. Report OOS (Out of Specification) , OOT (Out of Trend) results, and assist in root cause analysis & CAPA. Follow ALCOA+ principles for data integrity, as required in Indian pharma plants. 3. Laboratory Operations Ensure daily calibrations and proper operation of instruments as per respective SOPs. Maintain reference standards, working standards, volumetric solutions, and reagents as per Indian regulatory norms. Participate in Method Validation / Method Verification as per ICH Q2 guidelines. Adhere to lab safety, housekeeping, and proper waste disposal as per local pollution control guidelines. 4. Coordination & Cross-functional Support Coordinate with QA for batch release, document review, and deviations. Support Production in in-process testing and timely release of materials. Assist in external regulatory inspections (CDSCO, State FDA, WHO, Auditors, & Client Audits). Provide required analytical data during internal and external audits. Skills & Competencies: Strong understanding of Indian Pharmaceutical Regulations & GMP norms . Good knowledge of IP analytical methods and general chemical testing. Knowledge of instrument handling, troubleshooting, and calibration. Strong attention to detail and accuracy. Good communication and teamwork skills. Qualification & Experience: Education: B.Sc / M.Sc in Chemistry, Pharmaceutical Chemistry, or related field. Experience: 3–5 years in QC department of an Indian WHO-GMP certified pharmaceutical or nutraceutical manufacturing plant. Job Types: Full-time, Permanent Pay: ₹25,000.00 - ₹40,000.00 per month Benefits: Paid sick time Paid time off Provident Fund Work Location: In person
Job Title: Sales Manager – FMCG/ Nutraceutical Location: Delhi - Nerest metro Shalimarbough Mail - hr@medglobe.co.in Job Purpose The Sales Manager will be responsible for driving sales growth, developing markets, managing channels, and achieving revenue targets for the company’s Nutraceutical products. & FMCG Key Responsibilities Develop and implement monthly and quarterly sales plans Achieve assigned sales targets and revenue growth Appoint, manage, and support distributors, stockists, and channel partners Identify new business opportunities in domestic and international markets Build and maintain strong relationships with key customers Monitor market trends, competitor activity, and pricing Guide and motivate the sales team to improve performance Coordinate with marketing, supply chain, and regulatory teams Ensure compliance with company policies and industry regulations Prepare sales reports and forecasts for management review Required Qualifications & Experience Graduate / MBA preferred 6–10 years of experience in FMCG/ Nutraceutical sales Proven track record of achieving sales targets Strong knowledge of channel sales and market development Exposure to domestic markets; export experience is an advantage Good communication, negotiation, and leadership skills Willingness to travel extensively Key Skills Sales planning & execution Channel and distributor management Market expansion Team leadership Customer relationship management What We Offer Competitive salary with performance-based incentives Growth opportunities in a fast-growing organization Exposure to domestic and international markets Professional and supportive work culture Job Type: Full-time Pay: ₹35,000.00 - ₹75,000.00 per month Work Location: In person
Job Title: Quality Control Manager Department: Quality Control Location: Bhagwanpur Industrial Area Job Purpose The Quality Control Manager is responsible for managing and approving all Quality Control activities related to Chemical, Instrumentation, and Microbiology testing , ensuring compliance with regulatory and quality standards. Key Responsibilities Chemical Analysis Oversee testing of raw materials, in-process samples, and finished products Review and approve analysis reports, COAs, STPs, and test results Ensure compliance with pharmacopeia and internal specifications Instrumentation Control Manage analytical instruments such as HPLC, GC, UV, FTIR, AAS, Karl Fischer, Dissolution, pH, TOC etc. Ensure calibration, validation, IQ/OQ/PQ, and maintenance of instruments Review chromatograms, system suitability, and analytical data integrity Microbiology Control Supervise microbiological testing , environmental monitoring, water testing, and hygiene controls Review and approve microbiology reports and trends Ensure contamination control and compliance with microbiological standards Compliance & Documentation Ensure adherence to GMP, GLP, ISO, WHO-GMP requirements Maintain GDP-compliant documentation Handle OOS, OOT, deviations, and CAPA related to QC Audit & Team Management Support regulatory, customer, and internal audits Train and supervise QC analysts and microbiologists Coordinate with QA, Production, and R&D teams Qualifications & Experience M.Sc. (Chemistry / Microbiology) / B.Pharm / M.Pharm 8–12 years of relevant QC experience Mandatory hands-on exposure to Chemical, Instrumentation, and Microbiology QC Experience in audit handling and regulatory inspections Job Type: Full-time Pay: ₹45,000.00 - ₹75,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person
Business Coordinator – Sales (Female Candidate Preferred) [email protected] Location: Delhi- Near Shalimar Bough Metro Department: Sales & Marketing Reports To: Sales Head / Business Manager Job Purpose The Business Coordinator – Sales will support the sales team by coordinating daily sales activities, managing data and communication, and ensuring smooth execution of sales operations between field teams, management, and clients. Key Responsibilities Coordinate with field sales team for daily activities, meetings, and follow-ups Maintain sales data, MIS, orders, and customer records Prepare sales reports, presentations, and trackers Follow up on quotations, samples, orders, and dispatch status Act as a communication bridge between sales, accounts, logistics, and management Handle customer calls, emails, and WhatsApp communication professionally Support lead management and CRM updates Assist in sales planning, reviews, and target tracking Qualifications & Experience Graduate / MBA preferred 2–5 years of experience in sales coordination / business coordination Experience in Pharma / Nutraceutical / Healthcare is an advantage Key Skills Strong coordination & follow-up skills Good Excel & MS Office knowledge Professional communication (verbal & written) Multitasking & time management CRM handling (preferred) Working Days 6 days working What We Offer Professional work environment Growth-oriented role Stable career opportunity Job Type: Permanent Pay: ₹25,000.00 - ₹35,000.00 per month Benefits: Provident Fund Work Location: In person
Business Coordinator – Sales (Female Candidate Preferred) hr@medglobe.co.in Location: Delhi- Near Shalimar Bough Metro Department: Sales & Marketing Reports To: Sales Head / Business Manager Job Purpose The Business Coordinator – Sales will support the sales team by coordinating daily sales activities, managing data and communication, and ensuring smooth execution of sales operations between field teams, management, and clients. Key Responsibilities Coordinate with field sales team for daily activities, meetings, and follow-ups Maintain sales data, MIS, orders, and customer records Prepare sales reports, presentations, and trackers Follow up on quotations, samples, orders, and dispatch status Act as a communication bridge between sales, accounts, logistics, and management Handle customer calls, emails, and WhatsApp communication professionally Support lead management and CRM updates Assist in sales planning, reviews, and target tracking Qualifications & Experience Graduate / MBA preferred 2–5 years of experience in sales coordination / business coordination Experience in Pharma / Nutraceutical / Healthcare is an advantage Key Skills Strong coordination & follow-up skills Good Excel & MS Office knowledge Professional communication (verbal & written) Multitasking & time management CRM handling (preferred) Working Days 6 days working What We Offer Professional work environment Growth-oriented role Stable career opportunity Job Type: Permanent Pay: ₹25,000.00 - ₹35,000.00 per month Benefits: Provident Fund Work Location: In person