Provides occupational health services to employees across industries. Conducts pre-employment and periodic medical examinations for workers. Diagnoses and manages occupational diseases and work-related injuries. Assesses fitness-for-duty for hazardous work environments. Develops workplace health and safety programs and policies. Conducts worksite inspections and health hazard assessments. Manages EAP (Employee Assistance Programs) and mental health support. Collaborates with safety officers and ergonomists on workplace risks. Prepares medical reports for insurance and compensation claims. Trains employees on occupational health and safety awareness. Ensures compliance with Factories Act and occupational health regulations. Participates in industrial hygiene monitoring programs. Manages vaccination and health surveillance programs for workers.

Develops and implements community health programs and disease prevention initiatives. Conducts epidemiological surveillance and outbreak investigation. Manages immunization campaigns and public health interventions. Collaborates with government agencies on national health programs. Analyzes public health data for disease trends and risk factors. Designs health education and behavior change communication programs. Manages maternal and child health programs in rural and urban settings. Coordinates with ASHA workers, ANMs, and community health workers. Prepares public health reports and policy recommendations. Manages health data collection and HMIS reporting systems. Participates in disaster health preparedness and response planning. Builds partnerships with NGOs and CSOs for community health. Conducts health needs assessments and impact evaluations.

Coordinates and manages telemedicine consultation services for patients. Schedules and manages virtual OPD appointments across specialties. Trains doctors and patients on telemedicine platform usage. Ensures smooth video consultation experiences and technical support. Manages patient records, prescriptions, and digital documentation. Coordinates with pharmacy for digital prescription fulfilment. Monitors telemedicine adoption metrics and patient satisfaction scores. Resolves technical issues and escalates to IT team as needed. Ensures compliance with telemedicine guidelines issued by NMC and MoHFW. Builds referral networks with primary care providers for teleconsultations. Prepares weekly telemedicine utilization and performance reports. Coordinates follow-up consultations and specialist referrals. Manages telemedicine platform vendor relationships and improvements.

Manages hospital information systems, EHR, and digital health infrastructure. Oversees HMIS, LIS, PACS, and RIS system implementation and operations. Manages IT team responsible for hardware, software, and network support. Ensures 24/7 availability of critical hospital IT systems and applications. Develops IT strategy aligned with hospital digital transformation goals. Manages IT security, access controls, and data backup protocols. Implements and manages telemedicine and digital health platforms. Ensures compliance with data privacy and healthcare IT regulations. Manages vendor relationships for IT services and system contracts. Supports NABH and JCI digital health documentation requirements. Prepares IT budgets and manages capital and operational expenditures. Conducts IT risk assessments and business continuity planning. Trains staff on new IT systems and digital health tools.

Provides clinical and technical support for complex medical device products. Trains surgeons, nurses, and clinical staff on device usage and protocols. Assists in live procedures to ensure optimal product performance. Supports new product launches through clinical education programs. Demonstrates technical expertise and answers clinical queries from HCPs. Coordinates with R&D and clinical affairs on product improvements. Monitors device performance and reports clinical feedback to company. Manages pre- and post-sales technical support for accounts. Participates in clinical studies and data collection for devices. Develops clinical training materials and educational content. Attends medical conferences and presents clinical data on products. Maintains expert knowledge of competitive device landscape. Supports regulatory affairs with clinical evidence documentation.

Promotes and sells medical devices to hospitals, surgeons, and procurement. Conducts product demonstrations and in-service training for clinical staff. Provides technical support during surgical procedures as required. Achieves territory sales targets for device portfolio. Builds and maintains relationships with key surgeons and hospital administrators. Manages tender submissions and hospital formulary inclusions. Monitors competitive device landscape and adjusts sales strategies. Collects and reports adverse events and product complaints to vigilance team. Coordinates with clinical and marketing teams for product launches. Conducts clinical education sessions and CMEs for physician customers. Manages consignment inventory and instrument set management. Prepares monthly territory performance reports for management. Ensures ethical promotion aligned with MDR 2017 requirements.

Prepares and submits drug registration applications to CDSCO and state FDAs. Compiles Common Technical Documents (CTD) for global market submissions. Manages drug master files, certificates of analysis, and GMP certificates. Handles clinical trial authorizations and IND application filings. Monitors regulatory timelines and tracks submission progress. Responds to queries from regulatory authorities on pending applications. Manages license renewals, amendments, and post-approval changes. Stays updated on CDSCO notifications, drug alerts, and regulatory revisions. Reviews and approves labelling, package inserts, and patient information leaflets. Coordinates with international regulatory affairs teams on global filings. Manages regulatory database and filing systems for all products. Supports pre-submission meetings with regulatory health authorities. Trains team members on regulatory submission standards and tools.

Performs physical, chemical, and microbiological testing of pharmaceutical products. Analyzes raw materials, intermediates, and finished dosage forms. Operates HPLC, GC, UV spectrophotometer, and dissolution apparatus. Performs method validation and verification studies for analytical methods. Reviews and approves analytical data against specifications. Conducts out-of-specification (OOS) investigations and reporting. Maintains and calibrates analytical instruments in QC laboratory. Ensures compliance with ICH, USP, BP, and IP testing standards. Manages reference standards, working standards, and reagent controls. Participates in stability studies and ongoing stability programs. Maintains GLP in laboratory documentation and data recording. Supports regulatory inspections by preparing data and documents. Contributes to laboratory investigations and technical troubleshooting.

Develops and implements pharmaceutical quality management systems. Manages GMP compliance across manufacturing, packaging, and distribution. Oversees change control, deviation, CAPA, and OOS investigation processes. Reviews and approves batch manufacturing records and analytical reports. Manages supplier qualification and vendor audit programs. Ensures compliance with Schedule M, USP, BP, and ICH guidelines. Prepares site for CDSCO, USFDA, and MHRA regulatory inspections. Manages document control systems and SOPs across manufacturing. Reviews product complaints and coordinates market recall procedures. Develops risk management systems and quality risk assessments. Trains manufacturing and QC staff on GMP and quality culture. Participates in global quality governance and audits. Prepares Annual Product Reviews and quality trend analysis.

Conducts drug discovery and formulation research for new pharmaceutical products. Synthesizes and evaluates new chemical entities for therapeutic activity. Performs in-vitro and in-vivo pharmacological screening studies. Develops and optimizes drug formulations for target delivery systems. Conducts stability studies and stress testing of pharmaceutical products. Analyzes drug-excipient compatibility and physicochemical properties. Prepares scientific reports and contributes to regulatory dossiers. Manages laboratory notebooks, data integrity, and documentation standards. Collaborates with analytical, clinical, and regulatory teams. Operates analytical equipment including HPLC, GC, and spectrophotometers. Stays updated with IP landscape and files patents for novel discoveries. Participates in scientific conferences and publishes research findings. Mentors junior scientists and graduate research interns.