Responsibilities Conduct daily morning rounds for all in-patient department (IPD) patients and review prescriptions in wards and ICUs before dispensing. Lead the prescription audit team, ensuring thorough reviews and compliance with hospital policies. Collaborate with doctors to adjust doses for patients with abnormal pharmacokinetics and pharmacodynamics, particularly in cases of renal and hepatic impairment. Monitor restricted antibiotic use and coordinate with the infection control officer for the antibiotic stewardship program. Prevent, anticipate, and investigate potential drug interactions and adverse drug reactions, presenting monthly reports on these issues to the quality department. Monitor and implement the hospital’s narcotic policy, ensuring compliance. Regularly check and verify the contents of crash carts and disaster kits. Oversee blood sugar monitoring for all IPD patients and ensure timely incident reporting for any major incidents. Provide daily reports on medication errors, adverse drug reactions, incomplete prescriptions, dispensing errors, and patient counseling sessions. Ensure proper drug information is provided to both doctors and patients, with detailed counseling during patient discharge.Qualification & ExperienceEither Masters or Doctor of Pharmacy (Pharma D) is required Minimum 2 years experience.

ResponsibilitiesCollect, assess, and process adverse event reports to ensure accuracy and timely compliance with regulatory requirements Partner with cross-functional teams to address safety-related questions and support ongoing investigations Maintain current knowledge of pharmacovigilance regulations, global safety guidelines, and industry standards Manage safety inbox and acknowledge case receipt. Perform case triage and book-in to safety database. Enter case details accurately and write narratives. Code events, drugs, and medical history using MedDRA/WHO-DD. Apply correct product labeling and perform QC checks. Finalize case processing and generate queries for follow-up Knowledge of seriousness, expectedness, causality, and global reporting Familiarity with reconciliation processes and aggregate reporting (PSUR/DSUR) Ability to mentor new joiners and review SOPs Working knowledge of SDEA and KPI/SLA basics Process literature ICSRs and maintain compliance with monitoring requirements Qualification & ExperienceMinimum 2 years of experience in safety background, with direct involvement in case processing Solid experience in Post Marketing Surveillance/Clinical Trial case processing Bachelors degree in life sciences Strong analytical skills with attention to detail in data collection and reporting Excellent communication and interpersonal skills, enabling effective collaboration with team members and stakeholders A commitment to maintaining high standards of quality and compliance in all pharmacovigilance activities

ResponsibilitiesLead a team responsible for preparation and delivery of C&Q documentation supporting commissioning and qualification activities across Engineering projects and systems. Manage work across a blended team of employees and contingent resources, ensuring effective planning, prioritization, and execution of deliverables. Oversee development of qualification protocols, reports, risk assessments, traceability matrices, and related qualification documentation. Execute C&Q documentation preparation using established CoE standards, templates, and processes to ensure consistency, compliance, and efficiency. Partner with Engineering, Validation, Quality, Manufacturing, Facilities, and Project teams to support qualification execution and operational readiness activities. Monitor documentation progress, identify risks, and drive timely resolution of issues that may impact project timelines. Maintain inspection-ready documentation and support regulatory inspections and internal audits as required. Support implementation of standardized C&Q practices, templates, and procedures across Engineering projects and sites. Provide leadership, coaching, and development for team members while fostering a culture of accountability, collaboration, and quality execution. Contribute to continuous improvement initiatives that enhance C&Q documentation quality, efficiency, and compliance. Qualification & ExpeirenceBachelor’s or Master’s degree in engineering, Life Sciences, Pharmaceutical Sciences, or a related technical field. 8-13 years of experience in GMP commissioning, qualification, validation, engineering, or technical operations within the pharmaceutical or biotechnology industry. Experience supporting commissioning and qualification activities for manufacturing systems, packaging equipment, or facilities and utilities.

ResponsibilitiesBuild weekly, monthly, and end-of-contest reporting for assigned business units based on contest rules and eligibility criteria in IC platform. Execute data pulls, validation checks, and quality assurance to ensure accurate reporting for field teams and leadership. Translate contest rules into reporting logic, calculation steps, and data requirements. Partner with IC Design, IDNA, Field Reporting, and IC platform team to clarify assumptions and resolve data or logic discrepancies. Produce clear, analytical, and well-structured reporting outputs and summaries for business stakeholders. Maintain documentation of reporting logic, processes, and data sources. Support contest modelling, scenario analyses, and ROI calculations as needed. Identify opportunities to streamline recurring tasks through automation, templates, or improved workflows. Respond to field and stakeholder inquiries by investigating and explaining data or reporting variations.Qualification & Expeirence5-9 years of experience in Incentive Compensation.Relevant Bio/Pharmaceutical industry and/or consulting experience. Execution-Focused Delivery: Own and execute day-to-day analytics tasks, reporting development, and field data operations with speed, accuracy, and minimal oversight.

Responsibilities Execute the medical review of ICSRs (narratives, coding, expectedness, causality and seriousness) to ensure quality reports. Produce medically accurate ICSRs reports  Execute ICSR case escalation as appropriate  Execute appropriate case follow up per SOPs  Support medical coding conventions, and systematic process improvements for ICSR medical review  Conduct reportability assessment for medical device associated events and /or product complaint associated events, and review for potential product problems.  Support Quality Assurance of ICSR medical review (if applicable)  Provide input on teams for interdepartmental and cross-functional initiatives including, process improvement, standards development, Standard Operating Procedures (SOP) creation, and metrics with regards to medical review (if applicable)  Perform other duties related to the position as necessary as defined in SOPs or as requested by his/her supervisorQualification & Expeirence MD/DO or international equivalent and 1 year of related drug safety experience MD/DO or international equivalent plus 3 years of relevant work

ResponsibilitiesPrepare and manage IPQA shift rosters to ensure adequate coverage across all manufacturing and packing areas. Allocate qualified personnel based on activity criticality, workload, and skill matrix. Ensure no gaps during critical operations and maintain backup planning. Ensure IPQA presence during dispensing, granulation, compression, coating, and packing activities to maintain real-time compliance and control. Ensure proper line clearance before starting any activity. Verify equipment cleanliness, status labeling, and removal of previous product/material. Perform and monitor in-process checks such as weight variation, hardness, thickness, disintegration, and coating parameters as per BMR/BPR and SOP requirements. Conduct real-time and final review of batch documents to ensure completeness, accuracy, and compliance with US FDA expectations. Initiate and review deviations, out-of-specification (OOS), and out-of-trend (OOT) events. Drive root cause analysis and ensure effective CAPA implementation.Monitoring of reject handling on shopfloor. Tracking of in-process samples and ensuring timely release of areas for manufacturing and packing. Identification of opportunity of process and practice improvement on shop floor. Ensure all time compliance at manufacturing, packing and warehouse shop floor. Immediate reporting of observed non-compliance to IPQA In charge/ QA Head.Qualification & ExperienceB. Pharm/ M. Pharm/ M.Sc. With relevant experience in pharma. Must have knowledge of working on the shop floor as an in-process quality assurance. Exposure to various regulatory bodies such as US FDA, EU-GMP, MHRA, TGA Exposure to specific dosage forms like OSD.

ResponsibilitiesAs a Senior Analyst in Forecasting, you will collaborate closely with the GIBEx/GA&I Forecast Leader and Commercial teams to develop brand forecasts for strategic brands and early assets. Your role will involve understanding therapeutic areas, setting performance expectations, and guiding brand strategy. You will develop and maintain forecast models, lead forecasting processes, identify key business issues, and incorporate research results into forecasts. Additionally, you will align forecast assumptions with business partners and support continuous improvement in forecasting capabilities.Experience6+ years of direct Pharmaceutical forecasting experience with an in-depth knowledge of forecasting techniques, models and approaches Good understanding of multiple disease areas, with experience in rare diseases/OBU including how patients move through their respective diagnosis and treatment pathways, including treatment dynamics Experience integrating insights from market research and secondary data analysis into forecast assumptions Experience applying a range of data sources and analytics involving standard data in the Pharmaceutical industry – e.g. IQVIA (MIDAS, DDD NPA, Monthly Xponent), claims data (Truven, Marketscan), epidemiological data, etc. For US forecasting, experience with TRx / NBRx / NRx data and methodologies

Responsibilities Participate in KOM, project planning/strategy making meeting.  Ensuring the aggregate reports and RMP documents are medically relevant, complete, consistent and accurate.  Providing inputs/insights from review of aggregated and RMP data aligned to client’s processes(s) and SOPs.  Addresses all previous Health authority comments and adhoc requests received from Health authority.  Review and provide any noteworthy cases & published studies including pregnancy registries.  Discuss and provide medical analysis for all relevant sections of AR and RMP  To provide the conclusion regarding the current safety profile of the product.  Address all medical queries/comments raised by the Client.  Perform QC of all the assigned aggregate reports and RMP documents.  Complete all trainings, assigned by internally or client on respective LMS within due date.  Responsible for knowledge sharing, coaching, review and providing feedback of reports medically analyzed by the mentees.  Notify critical and major deviations (referred, as Quality Issues) within one business days, and minor deviations within three business days to Accenture Quality Management team. Ensure to meet all SLAs and KPIs.  Incorporate comments from Client (or external) stakeholders into the draft RMP/ associated documents and seek clarification where applicable.Qualification & ExperienceQualifications:MBBS/MD Years of Experience:3 to 14 years

ResponsibilitiesHead the Safety Evaluation And Risk Management Team Author/review/approve safety reports and maintain oversight Contribute to the development and implementation of Risk Management Plans including authoring/review/approval Review and oversight of Signal detection and evaluation activities Liaise and collaborate with other GPV functions, Global Glenmark affiliates and external business partners Review draft responses to regulatory authority/healthcare professionals queries as applicable Review literature search results for ICSRs and articles for inclusion in safety reports Participate in governance meetings Support product labelling activities Support audits, inspection and CAPA management relating to SERM activities Support assessment and implementation of regulatory intelligence impacting SERM activities Provide technical guidance in the development and maintenance of procedural documentation Support organizational initiatives in driving global operational excellence in Pharmacovigilance Support the QPPVsQualification & ExperienceMD/MBBSYears of experience: 16-18 years

ResponsibilitiesLiterature search and study designing of Bioavailability and Bioequivalence studies of oral & non-oral products towards different regulatory submission. Review of BA/BE study protocol and provide Pharmacokinetic (PK) inputs into the study protocols Coordinate with the CRO for finalizing pilot and pivotal biostudy protocol for DCGI BE application. Develop protocol for patient based BA/BE studies & PD end point study for complex generics. Perform PK and Statistical analysis of in-vivo data obtained from BA/BE and pharmacokinetics studies using Phoenix Software. Use modeling & simulation tools for study optimization. Respond to regulatory queries related to PK analysis and study interpretation.  Qualification & ExperienceGraduate : M.Pharm /Pharm D Experience Tenure : Minimum 3 years of relevant experience