ResponsibilitiesSupport the Pharmacy Manager in overseeing the daily operations of the Pharmacy Department. Review, interpret, and dispense prescriptions while ensuring medication appropriateness and maintaining accurate records. Maintain proper handling and documentation of controlled medications, including narcotics and psychotropic substances. Assist in implementing pharmacy policies, quality programs, and professional standards such as GPP/GMP practices. Manage medication inventory, including procurement, stock monitoring, storage, and stock rotation to ensure adequate supply. Provide drug information and medication counseling to doctors, healthcare professionals, and patients. Support safe preparation and handling of cytotoxic medications and ensure proper waste management procedures. Participate in ward clinical pharmacy services, including medication review during ward rounds, medication history review, and bedside dispensing. Supervise and guide Pharmacy Assistants to ensure smooth pharmacy and ward operations. Monitor and report adverse drug reactions and ensure compliance with regulatory requirements. Assist in evaluating new drug requests and maintaining the Hospital Drug Formulary. Support clinical research activities and liaise with pharmaceutical companies or clinical organizations when required.Qualification & Experience       Bachelor of Pharmacy Registered Pharmacist with valid annual retention certification CDR (Chemotherapy Drug Reconstitution) or Clinical Pharmacy experience will be advantage Proficient in both spoken and written English.

ResponsibilitiesClinician recruitment, engagement & management Clinical quality & performance Clinical Strategy, effectiveness/audit and outcomes Clinical Governance and Operations Academics and Research Training and Communication Effective Clinical Utilization Medical Capex, Budgeting and Approvals Medical Statutory (monitoring)& Medico Legal Reports and MIS Work relations, analysis and actions. Qualification & ExperineceQualification: MBBS +MHA/PG (Hospital Administration) Experience: 8-10 years (out of which 3 years as a DMS with 200 bedded Hospital)

ResponsibilitiesImplementation of quality standards across the unit. Achieving accreditation and certifications with minimum observations. Conduct of quality improvement projects. Ensure data integrity for quality management by meticulously capturing and verifying key quality indicators. Accurate and timely publishing of reports.Qualification & ExperienceQualification: MHA(Mandatory) Experience: 5 years

Responsibilities Performance in Nursing Assignments Compliance to SOP and department's protocol. Customer Satisfaction Skill and Knowledge Application Team Supervision and Development Review and Implementation of New Techniques and procedures Department administration Qualification & ExperienceCandidate with BSc/MSc Nursing Registered under State Nursing Council 10+ years of experience for MSc 15+ years of experience for BSc

Qualification & ExperienceQualification: MBBS + MD/DNB Anaesthesia Experience: 0–5 years in a hospital/healthcare setup

ResponsibilitiesManage and monitor patients on hospital floors Provide timely medical care and clinical assessments Coordinate effectively with consultants and nursing staff Ensure accurate documentation and adherence to clinical protocols Handle emergency situations efficiently.Qualification & ExperienceQualification: MBBS & valid registration Experience: Minimum 1+ years of relevant clinical experience

Qualification & ExperienceQualification: Graduate/ Post Graduate Experience: 2 to 6 YearsNote: Candidates with MT Experience in Radiology is required.

ResponsibilitiesPrepare, review, and maintain Artwork-related activities for India Region Formulations in compliance with regulatory and corporate requirements. Prepare and review of specification and STP of Raw material, Packing Material and Drug Product. Update and manage all required QMS and documentation activities in Veeva Vault, ensuring data integrity and timely compliance. Perform audits as and when required and provide support in the preparation and finalization of audit reports (US and IR Formulation). Review raw data and analytical reports of contract manufacturing products to ensure accuracy, compliance, and adherence to approved specifications.Qualification & Experience8-12 years in relevant area as mentioned in the Job descriptionGraduation Post Graduation in Pharmacy or Science

Responsibilities Supervise compliance of CGMP, GxP and any other applicable regulatory requirement, including EH&S requirements.  To ensure timely updation of all logbooks of Purified water systems of Block1, Block3, Block4, Quality Control and Potable Water system.  To handle QAMS, EDMS, Caliber E-log related activities of engineering department. Allocation of Jobs to technicians and issuing of spares, if required from engineering stores.  To perform HVAC revalidation as per planner.  Operation and maintenance of HVAC System and Purified Water System.  Raising of purchase indents for spares, Clearance of GRN.  Preparation of GMP documents like Equipment qualification, SOPs etc. of HVAC System and Purified Water System.  Preventive Maintenance of HVAC / Water system equipment as per schedule and WCOM of PM orders in SAP.  To ensure sectional training compliance of workmen in CETMS.  Shift Breakdown Maintenance. 

ResponsibilitiesPreparation of SOPs/ STPs for Raw Material/ Packaging Material/Consumable material and preparation of Raw Material/ Packaging Material/Consumable material specifications as per QC format after receipt from R&D. To update Specifications/ STPs in line with the Pharmacopoeial changes. Timely sampling/ testing with online documentation of Raw Material/ Packaging Material/Consumable material as per approved specifications/ test procedures. Timely shipment and tracking of RM/ PM samples to commercial laboratories for the outsourced test parameters. Management of RM/ PM retention/ reserve samples and their related documents. Routine sampling of water as per the approved sampling schedule following the approved sampling procedures and perform timely testing with online documentation. And preparation of trends of water samples as per the approved frequency. Preparation of equipment URS/ Qualification protocols/ reports pertaining to Raw Material/ Packaging Material. Preparation and execution of study protocols and reports pertaining to Raw Material/ Packaging Material.Qualification & Expeirence2 to 3 years Education Masters in Chemistry or Organic Chemistry