ResponsibilitiesTo maintain inventory level of the department. To store pharmaceuticals at optimum condition as to minimizes expiry. To control drug purchases cost by negotiations and contracts. To deliver quality services of pharmacy department to clients and employees. To give dispensing of medications with clear instructions and correct labeling to patients. To provide clear, understandable instructions to discharge patients in a language known to patient with information leaflets if possible. To act as a liaison with nursing and medical staff concerning prescriptions orders, drugs and pharmaceutical details, resident reactions, errors and complaints. To maintain departmental policies and procedures, objectives, quality assurance program, safety, environment and injection control standards. To have secure storage of narcotics and other controlled substances on a regular basis.Qualification & ExperienceBACHELOR IN PHARMACY / DIPLOMA IN PHARMACY EXPERIENCE : 2 YEARS OR MORE

Responsibilities To provide list of Chemicals & Reports of Purchase Department after approval of H.O.D..  To attend all O.P.D. & I.P.D. Patients.  To conduct all routine tests for all surgeries(including Lapchole, Holep, PCNL, BNI,ESWL etc)  To type all tests reports of all OPD & IPD Patients & signed by H.O.D..  To follow strict biomedical waste management segregation e.g. Needle cutting & Waste checking.  To maintain test report register of all O.P.D. & I.P.D. Patients.  To take care of the equipments and to co-ordinate with biomedical team for the same.  To give priority to emergency cases and to co-ordinate with the consultants / respective department for the same.Qualification & ExperienceDEGREE / DIPLOMA IN MEDICAL LABORATORY TECHNOLOGY EXPERIENCE : 1-5 YEARS

ResponsibilitiesKeeps the Patient Appointment Folders ready in coordination with the MRD and support staff. Ensures Billing coordination and mapping the vouchers equivalently with the respective patient folders. Observes patients physical condition and emotional changes and adequately reports the same to registered nursing professionals. Utilizes techniques of reality orientation when dealing with disoriented or potentially disoriented patients, maintains a safe, clean comfortable hospital environment. Recognizes potential environmental safety and health hazards, assists in implementing hazard prevention methods and disaster plans. Knows the infectious process and modes of disease transmission and assists in ensuring effective infection control practices during patient care. Assist with physical and diagnostic examinations. Any other duties that may be assigned from time to time by the nurse in charge. Coordinate with the medical officers as required. Coordinate with the Hospital attendants for Palliative patients shifting. Is responsible for Patient Linen management and patient mobility assistance as needed.Qualification & ExpeirenceBSc, Additional Qualification in Computer applications will be an advantage Experience: Fresher's can also apply.

Qualification & ExperienceQualification: MBBS+MD/DNB/FNB/FCPS/DA/Diploma in Pulmonary/Respiratory/General Medicine/Emergency/AnaesthesiaExperience: 0 to 4 years

ResponsibilitiesProject co-ordination RTPCR testing and reporting Data analysis Maintaining budget and personnel Patient recruitment Co-ordination with diagnostics for relevant testsQualification MSc (Microbiology) or PhD

ResponsibilitiesLiterature study for applications of specific product and data compilation. To perform lab trials related to food/premix applications and conduct stability study. Preparation of premixes as per requirements received from marketing team and to send for analysis and to customer for trial purpose. New product designing including calculations for label claims and respective sources, nutritional values and related aspects. To perform calibration of lab instruments and equipment’s. Maintain documents of lab trials, analytical reports, samples dispatched, marketing queries, audits and routine work requirements. To follow up and review of pending analysis samples and documents. Procurement of new raw materials as per requirement. To ensure compliance of safety measures. Imparting and organizing the internal training activities for HNH and ANH department concern people. To ensure compliance to audits. To ensure avoidance of breach of data integrity. Responsibility of the producing quality products & maintaining quality.

ResponsibilitiesHelps in demonstrating the operation in case of a new machine or a new pack-profile is implemented. Preparation of protocol for validation/qualification pertaining to Process, Cleaning, Equipment and area/HVAC Execution of validation/qualification activities Coordination with different departments for performing validation/qualification activities Compilation of data and report preparation Maintaining documents as per Document control policy Lessoning with FDA for manufacturing licenses and certificates.Qualification B.Pharma/M.Pharma/ B.Sc

ResponsibilitiesHelps in demonstrating the operation in case of a new machine or a new pack-profile is implemented. Handling of Vendor Management System Familiar with Protocol and report preparation. Well familiar with document and Data control and alternate vendor development related documentation as per cGMP requirement. Exposure to QMS software like TrackWise, ENSUR, SAP is preferredQualification & ExperienceMinimum Graduate / Post Graduate with Pharmacy /Chemistry, having exposure to work in Regulated OSD industry is preferred.

Responsibilities Review and guide the team in preparing dossiers for Europe, Australia, New Zealand, and Canada (EANC) regions.  Review and guide the team in responding to queries from regulatory agencies and customers in the EANC region. Liaise with R&D, manufacturing plants, clinical teams, and respective EANC offices/BD teams. Support the lifecycle management of EANC registered products by achieving variation approvals. Maintain departmental databases. Regularly study regulatory guidelines and stay updated on Electronic eCTD (electronic Common Technical Document) requirements.  Maintain and submit GMP (Good Manufacturing Practice) applications.

ResponsibilitiesEnsure readiness of equipment and instrument for process. Ensure availability of the process Raw materials, accessories and consumables in process area before batch execution. Preparation, Review of process, equipment and area related SOPs and EOP's. Preparation and execution of process, area and equipment qualification / validation protocols. Preparation of various reports like process, equipment, area qualification and validation. Preparation and Review of BPR. Request and Issuance of BPR. Preparation, Review and execution of study protocols. Readiness of downstream area and other areas like corridors and washing area etc. for manufacturing operations. To ensure smooth functioning of shop floor functions during manufacturing campaigns. To raise and review change control and deviations as per the requirement.Qualification & ExperiencePost Graduation B.Tech in Biotechnology or Biochemistry11 to 16 years of experience