ResponsibilitiesLead brand and marketing strategy for Vazokare Cardio portfolio; drive growth, new launches, and lifecycle management; manage product teams, campaigns, and digital initiatives; coordinate cross-functional execution; ensure regulatory compliance; and build high-performing teams.Qualification & Experience 18+ years of pharmaceutical marketing experience in cardiology; strong commercial and analytical skills; proven leadership; Science/Pharmacy degree (MBA preferred).

ResponsibilitiesProvide scientific and medical support across the organization; develop and review medical content; support medico-marketing activities; ensure regulatory and promotional compliance; manage KOL interactions and medical queries; conduct literature research; and contribute to clinical and competitive intelligence.Qualification & Experience M.Pharm or Pharm D (Pharmacology); pharmaceutical industry experience.

ResponsibilitiesDevelop and optimize pharmaceutical formulations through lab and pilot scale; conduct pre-formulation and compatibility studies; support scale-up, exhibit batches, and technology transfer; prepare development and regulatory documentation; and collaborate with QA, QC, Production, and Regulatory teams to ensure quality, compliance, and timelines.Qualification & Experience 3–8 years of experience in pharmaceutical Formulation & Development; M.Pharm/PhD in Pharmaceutics preferred.

ResponsibilitiesMedication Preparation: Dispense, reconstitute, and label medications, IV fluids, and anesthesia agents required for surgeries. Inventory Management: Monitor stock levels for controlled substances, emergency crash carts, and surgical drugs, ensuring zero stock-outs. Safety & Compliance: Enforce NABH and hospital safety standards, specifically regarding aseptic techniques and controlled substance logs. Cross-Functional Collaboration: Coordinate directly with anesthesiologists, OT technicians, and nursing staff regarding real-time medication needs during procedures. Audit & Expiry Control: Regularly check medications for expiration dates and proper storage conditions.

ResponsibilitiesPharmacy OperationsManage day-to-day operations of inpatient, outpatient, emergency, and specialty pharmacies.Ensure accurate dispensing and distribution of medications as per physician prescriptions.Maintain adequate stock levels of medicines, consumables, and pharmacy supplies.Monitor drug utilization and minimize medication errors.Inventory & Supply Chain ManagementPlan and monitor procurement of medicines and surgical consumables.Coordinate with vendors and suppliers for timely procurement.Monitor stock expiry, near-expiry products, and slow/non-moving inventory.Ensure proper storage conditions for drugs, narcotics, vaccines, and temperature-sensitive items.Regulatory ComplianceEnsure compliance with Drugs and Cosmetics Act, Pharmacy Act, NABH standards, and other applicable regulations.Maintain all statutory licenses and records.Oversee controlled drug management and documentation.Ensure periodic audits and compliance reviews.Team ManagementSupervise pharmacists, pharmacy assistants, and support staff.Prepare staff schedules and duty rosters.Conduct performance evaluations and training programs.Ensure adherence to pharmacy SOPs and hospital policies.Quality & Patient SafetyImplement medication safety initiatives.Monitor adverse drug reactions and medication incidents.Participate in hospital quality improvement programs.Ensure proper labeling, dispensing, and patient counseling practices.Financial ManagementMonitor pharmacy revenue, expenses, and profitability.Control inventory carrying costs and wastage.Prepare departmental budgets and reports.Analyze pharmacy performance indicators and cost-saving opportunities.Coordination & CommunicationCoordinate with clinicians, nursing teams, procurement, finance, and quality departments.Support formulary management and drug evaluation activities.Assist in introducing new medications and treatment protocols.

ResponsibilitiesReview and interpret inpatient medication orders prescribed by doctorsDispense correct medications with proper dosage, route, and timingEnsure accuracy in medication preparation, labeling, and distributionMaintain strict compliance with hospital protocols and pharmacy regulationsMonitor drug interactions, allergies, and contraindications (in coordination with clinical team)Coordinate with nurses and doctors regarding medication changes or clarificationsMaintain stock of inpatient medicines and ensure timely replenishmentTrack controlled drugs and maintain legal documentation as per regulationsEnsure proper storage conditions for all medicines (temperature, expiry, etc.)Maintain daily dispensing records and pharmacy documentationQualification & Experience B.Pharma

ResponsibilitiesPreparing and submitting the accountability list to the Asst. Manager of pharmacy on a regular basis.Responsibility for patient counseling.Responsibility for preparation of MIS report and related documentation on a regular basis.Coordinating manpower allocation as per need.Handling customers and discharging prescriptions.Attending to home delivery calls.Responsibility for reducing dispensing time. Additional responsibilities entrusted by the units.Daily medicine bounces registerRack material accountability reportsCostly medicines handover accountability reports

ResponsibilitiesClinical ResponsibilitiesReview and validate oncology prescriptions for appropriateness, dosing accuracy, drug interactions, contraindications, and treatment protocols.Verify chemotherapy, immunotherapy, targeted therapy, and supportive care medication orders.Participate in multidisciplinary tumor boards and clinical rounds.Monitor patients for adverse drug reactions, toxicities, and treatment-related complications.Recommend dose modifications based on laboratory parameters, organ function, and patient-specific factors.Ensure compliance with established oncology treatment guidelines and protocols.Provide pharmacotherapeutic recommendations to physicians and healthcare professionals.Medication ManagementSupervise and ensure safe preparation, handling, storage, and dispensing of cytotoxic medications.Maintain compliance with chemotherapy safety standards and hazardous drug handling guidelines.Review medication reconciliation during admission, transfer, and discharge.Monitor inventory and utilization of high-cost oncology medications.Assist in formulary management and medication procurement activities.Patient Counseling & EducationCounsel patients and caregivers regarding chemotherapy regimens, medication administration, side effects, precautions, and adherence.Educate patients on supportive care medications and symptom management.Provide written and verbal medication information and follow-up guidance.Quality & SafetyParticipate in medication safety initiatives and quality improvement programs.Report and document medication errors, adverse drug reactions, and near-miss incidents.Conduct audits related to oncology pharmacy practices and chemotherapy administration.Ensure compliance with NABH, JCI, and other regulatory standards.Documentation & ResearchMaintain accurate clinical documentation and pharmaceutical interventions.Participate in clinical research, drug utilization reviews, and pharmacovigilance activities.Assist in developing and updating oncology treatment protocols and policies.Contribute to continuing education and training programs for healthcare staff.Qualification & Experience  Pharm D Registered Pharmacist with the State Pharmacy Council.Certification or specialized training in Oncology Pharmacy preferred.

Qualification & ExperienceD.Pharm / B.Pharm Experience: Fresher / Experienced

ResponsibilitiesOverall responsibilities for quality assurance compliance at the Zydus Hospira Oncology Private Limited (ZHOPL) site and Pfizer Quality at & ensure sustainable GMP compliance for Pfizer Products manufactured at ZHOPL site as per Quality agreement.Batch record review and release authorization compliance functions:Responsible for review and authorize the packed batch lot(s) for distribution in respective market from ZHOPL.To be part of SQRT as needed for any Batch related issue discussion.Regulatory impact assessment for all types of change related to Pfizer productsResponsible for Review and approval of Change controls at ZHOPL as per the Pfizer requirements.Responsible for performing the SCNM (Site Compliance Network Member) activities at ZHOPL and create the PAC and PCF in the PDM systems.Responsible for the review and approval of submission package as per procedure REG-459.Review BoH Queries & response and compendial/scientific data changesResponsible for review and approval for NPL assessment and dossier handover to ZHOPLComplaint Management for Pfizer ProductTo coordinate and ensure that ZHOPL comply with the requirements for managing complaint.To review and approve the ZHOPL complaint investigation reports and upload investigation reports in the Pfizer electronic complaint database.Support for activities including co-ordination committee meeting and share the applicable information/ distribution details to site & & Pfizer market action leader function during market action and mock recall activity.Quality Management System (QMS) compliance functions: Responsible for Review and approval of Investigations (QARs) initiated at ZHOPL. To be part of SQRT and involve in the Investigations. Provide support for Supplier management. To provide Quality support for review of documents for new product launches and Tech transfers as needed Responsible for reviewing and approval of Process validation related performed at ZHOPL.Other: To support any additional and urgent activity in absence of primary responsible person as assigned by the Manager. Responsible to support with the AQRT /ESQRT process as and when required. To provide Quality support for new product launches and Tech transfer as and when neededPfizer Revolution Global SOPs management activities: Responsible for role of LPO for processes for Pfizer, Accountable for local process performance. Several LPOs could be assign to each L2 process, depending on local process requirements.Any other responsibilities assigned by the Manager.Qualification & ExperienceB. Pharm/ M. Pharm / M.Sc.10+ years of pharmaceutical industrial experience.Exceptional organizational and project management skillsDemonstrated strength in analytical skills and meticulous attention to detailA solid understanding of the regulatory and audit frameworks pertinent to biopharmaceutical operationsProficiency in taking decisive action based on quality and compliance metrics and trendsCapable of managing multiple complex projects with a strong sense of business acumenExcellent interpersonal effectiveness, coupled with superior written and verbal communication skills