ResponsibilitiesDaily ward round through out the hospital, Auditing the medicine chart,Cross checking the medicine card with consultant notes, Checking the indent and dispensing,Monitoring of proper administration,Reporting the medication errorChecking medicines storage and usage,Narcotic audit,Crash cart audit,Storage condition and Inventory checking,Sound Alike & Look Alike medicine storage,Training for nursing staffs, MO's and technicians,Restricted antibiotic usage monitoring,Drug drug interaction monitoring,Adverse drug reaction monitoring,Coordinating with work related to compliance of JCI and formulating the policies as per requirements. Qualification & Experience      Able to work accurately and with minimal supervision.Ability to comprehend written instructions given by the Doctors and the other related departmental personnel.Ability to plan & organize ones work schedule effectively.Speaking and listening are essential requirements to understand and carry out the instructions given by the supervisors and other related departmental personnel.Affinity to work in team.Enthusiasm.

Responsibilities Literature 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 in India and outside India for finalizing biostudy pilot and pivotal study 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.  Literature 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 Qualification & ExperienceM.Pharm Experience Tenure : 4-6 years

Responsibilities• You will be responsible for the promotion of the new product. You will be executing the Product Management Team’s marketing strategy, analysing market trends, consulting with doctors on new product potential, and relaying feedback to the Product Management Team. Additionally, responsibilities include identifying key opinion leaders, monitoring product availability, and implementing brand strategies to facilitate a successful product launch.• You will be responsible for monitoring primary and secondary sales through regular visits to stockists and pharmacies, ensuring the accomplishment of doctor and product-specific sales objectives. Active participation in monthly review meetings to assess coverage, adherence to SOPs, and expense management, all aimed at achieving area-level, product-level, and overall sales targets.• You will be responsible for focusing on customer relationship management, the role entails establishing strong connections and addressing queries promptly using Infoginip. It also involves customer classification based on potential, determining meeting frequency accordingly, and tracking return on investment per customer to foster a loyal customer base for the company.• You will responsible to meet Key Opinion Leader (KOL) and Key business leader (KEL) frequently and pursue them to conduct CME with the company; Collect interest areas of key customers and hospitals and conduct CMEs on those topics.• You will responsible to prepare product matrix depending upon doctor's potential & preference and decide which product will fit doctor's need. Update data on chemist, doctors and Retail Chemist Prescription Audit (RCPA) through palm top to Unnati portal in order to ensure all stakeholders' access to latest information.Qualification & Experience• Educational qualification- Graduate with science background.• Minimum work experience- 6 months of experience in pharmaceutical sales.• Basic understanding of pharmaceutical products and marketing• Experience in implementing and analysing sales and marketing strategies.• Basic knowledge of Computers.• Excellent communication and interpersonal skills.• Good at building and leveraging relationship.• Strong analytical and problem-solving abilities.• Strong Decision making skills.

ResponsibilitiesMedical Strategy & PlanningExecute the Medical Affairs plan for DRL new product launch in EM countriesProvide strategic inputs to cross-functional teams including marketing, strategy, regulatory, portfolio and clinical developmentSupport the creation of target patient profiles, CLM contents and contribute to product differentiation strategiesScientific Engagement & CommunicationBuild and maintain relationships with a set of KOLs globally and support country teams (MSL/ commercial) to address HCP queriesOrganize and lead COE-driven scientific events such as advisory boards, global webinars, and ISPsDisseminate scientific updates at internal and external meetings on product and therapy areaEvidence Generation & PublicationsSupport DRL sponsored or investigator initiated studies, real-world evidence generation, and post-marketing surveillance, as and when requiredContribute to scientific publications, conference proceedings, and subsequent development of HCP communication on those studiesOther Core Internal and Administrative SupportReview and approve promotional materials/ events/ FMV calculation/ KOL tiering and ensure compliance with SOPs and regulatory standardsConduct training sessions for internal teams (MSLs/ commercial) on disease area, product knowledge, guidelines, differentiation etc. at regular intervalProvide scientific and clinical support to sales, marketing, portfolio and strategy teamsMarket Insights & Future Strategy DevelopmentGather and analyse customer insights and market trends to further strengthen medical and commercial strategiesEvaluate new products and provide medical rationale for portfolio expansion in related disease areaSupport digital content creation, review, and approval for DRL platforms and leverage technology for scientific exchange and stakeholder engagementQualification & ExperienceMBBS + MD Pharmacology from a recognized medical institute in IndiaMinimum 2 years of experience in Medical Affairs in pharmaceutical industryMust have prior experience in handling products in Diabetes and Cardiovascular therapy areas, preferably launching novel entitiesGood understanding of clinical research, medical statistics, regulatory standards, and therapeutic area expertiseExcellent English communication, presentation skills, and project/stakeholder management skills.

ResponsibilitiesYou will be responsible to provide tactical and strategic inputs, and business/technical expertise, to Product Management towards ethical promotion of assigned products, in the operational areas listed.You will be responsible for providing strategic inputs for marketing and brand plans, overseeing the design and execution of medical-marketing programs, and facilitating interactions with healthcare professionals.You will be responsible for developing, reviewing, and approving protocol documents and supporting materials for various clinical projects.You will be responsible to provide useful, timely, accurate, and balanced medical information to internal (sales staff) and external customers.You will be responsible for training the Sales Force on basic sciences/assigned products and pre-launch and launch training for new products.You will be responsible to develop and share expertise in identified medical and/or scientific therapeutic areas.You will be one-point Medical Affairs contact for Customer Relationship Management and operational liaison in various functional domains.You will be responsible forfostering a culture of learning and development and managing the Medical Affairs staff, providing training, guidance, and support across various functional domains.You will be responsible to support the cluster Head Medical Affairs in budgeting, provisioning, and expense control.Qualification & ExperienceEducational QualificationPost-graduate degree in Pharmacology or other Medical specialty/ Graduate degree in MedicineMinimum Work Experience6-10 years of relevant experience in medical affairs handling brand medical strategy with at least 2-3 years in a people management roleBasic knowledge of the pharmaceutical industry, drug discovery, research & development, commercialization, promotion, and applicable policies, procedures, regulations, and guidelines.Expertise in clinical trial design and methodology, and understanding of interfaces, and conduct.Communication skills, both written and verbal (including medical writing and presentation skills).Interpersonal skills, internal & external networking, and the ability to impact and influence.Analytical skills and reasoning, and sound medical judgment/decision making.

ResponsibilitiesTo ensure cGMP and compliance review in the manufacturing shop floor and packing areas. To supervision of dispensing activity of manufacturing shop floor and packing areas. To Issuance of Bottle label, Ouster and Medication guide for commercial batch. Rsponsible for providing machine and area clearance. To conduct Sampling of reserve sample, stability sample and In-process checks during execution of batch packaging as per Batch Packaging Record (BPR) and stability study protocol. Online Documents and records review like equipment’s logbooks, dispensing logs, housekeeping records, environmental monitoring records, calibration record, batch records etc.. Calibration of IPQA instruments.Qualification & ExperienceMaster Degree (MS/MA) M. Sc - Microbiology Experience 2 years or more in 2 - 4 Years

Responsibilities Manage, control, and maintain all Quality Assurance (QA) documents, records, and logs in compliance with GMP requirements.  Ensure timely issuance, retrieval, archival, and destruction of controlled documents according to approved procedures.  Maintain document revision history and ensure only current, approved versions are available for use.  Coordinate document review, approval, and distribution processes with QA, Production, QC, and other departments.  Monitor compliance with document control procedures and support internal audits and regulatory inspections.  Maintain electronic and physical document management systems, ensuring data integrity and confidentiality.  Track periodic review schedules for Standard Operating Procedures (SOPs), specifications, forms, and quality manuals.  Support change control activities by updating and distributing revised documents as per approved changes.  Prepare document control metrics, reports, and status updates for management review.  Ensure all documentation practices comply with applicable regulatory guidelines, including GMP, WHO, FDA, MHRA, and company quality standards. Qualification & ExperienceB. Pharm B. Pharm - Required M. Pharm M. Pharm - Preferred Experience: 2 years or more in 2 - 5 Years

ResponsibilitiesResponsible for overseeing and performing daily case processing of adverse event cases (clinical trial and/or post marketed), including coding using MedDRA, determining seriousness and expectedness at the event and case level. Perform case follow up activities such as identification of information to be collected during follow-up. Creating and reviewing case narratives. Providing client notifications as required for case management. Supporting and contributing to the development of training materials and training delivery. Highlight areas of concern/discrepancies to the Principal PV Specialist, Case Processing and/or Manager, Case Processing when related to ICSRs. Acquire and maintain an up-to-date knowledge of global safety regulations for medicines. Peer reviews of cases for quality, consistency, and accuracy. Provide oversight and direction of PV deliverables as a PV subject matter expert as needed. Perform Health Care Professional (HCP) review (as required). Mentors and trains less experienced staff. Other duties as assigned.Qualification & ExperienceRequired: a Bachelor's degree in life sciences. Preferred: an advanced degree, RN, RPh, PharmD or equivalent.

ResponsibilitiesManage assigned mailboxes, including inbox triage of client communication, inbound reports, and internal case processing communications. Perform Duplicate searches and complete initial book-in as required. Screen and redact the source documents for PHI as per company procedures. Facilitate literature related activities as needed. Initial triage of regulatory authority database searches. Send draft reports to clients for review as needed. Enter basic data into safety database as required such as identifiable patient, report, suspect drug, and adverse event. As applicable perform full data entry into safety databased with proper experience and training. Other duties as assigned.Qualification & ExperiencePost-secondary education.Preferred: one year of industry experience.

Responsibilities Coordinate and schedule all meetings with cross-functional stakeholders to ensure effective collaboration and alignment  Drive report timelines and escalate risks or delays to team leads or management  Collaborate with cross-functional stakeholders and external business partners to collect PASR contributions and compile into PASR template.  Author safety content for all PASRs in collaboration with Therapeutic Area Safety scientists  Conduct peer QC of safety authored sections, coordinate Amgen review and resolve comments and initiate approval workflows.  Maintain and archive accurate records and documentation throughout the report process.  Review and approve published report versions (i.e. blinded, unblinded, EU FDA, Rest of World).  Manage report distribution to Contract Research Organizations (CROs) and Business Partners (BPs)  Ensure adherence to established timelines, regulatory guidelines and applicable standards, styles, guidelines and processes  Peer review/quality review of all PASRs within established timelines with adherence to applicable guidelines and processes, using appropriate checklists  Maintain and develop current knowledge of regulatory guidelines, technological advances and industry standards  Generate PASR metrics, including Key Compliance Indicators (KCIs) and Key Performance Indicators (KPIs).