Responsibilities Enter information into PVG quality and tracking systems for receipt and tracking ICSR as required. Assists in the processing of ICSRs according to Standard Operating Procedures (SOPs) and project/program-specific safety plans as required. Triages ICSRs, evaluates ICSR data for completeness, accuracy, and regulatory report ability. Enters data into safety database. Codes events, medical history, concomitant medications, and testsCompiles complete narrative summaries. Identifies information to be queried and follows up until information is obtained and queries are satisfactorily resolved. Assists in the generation of timely, consistent, and accurate reporting of expedited reports in accordance with applicable regulatory requirements. Maintains safety tracking for assigned activities. Performs literature screening and review for safety, drug coding, maintenance of drug dictionary, MedDRA coding as required. Validation and Submission of xEVMPD product records, including appropriate coding of indication terms using MedDRA. Manual recoding of un-recoded product and substance terms arises from ICSRs. Identification and management of duplicate ICSRs. Activities related to SPOR / IDMP. Quality review of ICSRs. Ensures all relevant documents are submitted to the Trial Master File (TMF) as per company SOP/Sponsor requirements for clinical trials and the Pharmacovigilance System Master File for post-marketing programs as appropriate. Maintains understanding and compliance with SOPs, Work Instructions (WIs), global drug/biologic/device regulations, GCP, ICH guidelines, GVP, project/program plans and the drug development process. Fosters constructive and professional working relationships with all project team members, internal and external. Participates in audits as required/appropriate. Applies safety reporting regulatory intelligence maintained by Syneos Health to all safety reporting activities. Qualification & ExperienceEducation: B.Pharm/M.Pharm onlyExperience: Minimum 1 year of experience in PMS and Spontaneous cases Preferred Database: LSMV, fine to proceed with Argus Safety Database systems and knowledge of medical terminology required.

Responsibilities Oversee and support the overall activities during the product development life cycle from Quality perspective in R&D (API and intermediates)  To judge and understand the site needs with respect to system establishment and sustainability.  Author / Review the SOPs/work directions required for implementing the Quality Systems in R&D activities as per GLP and regulatory requirements. Ensure effective implementation of SOPs/ work directions.  Review and approve technology transfer, product specification, analytical method validation, method transfer, qualification, calibration, process validation protocol and reports. Ensure effective execution of these activities.  Periodic audits of R&D laboratory. Ensure online documentation and review lab notebooks, PDR/LFR documents, analytical documents and stability data.  Effective maintenance of R&D records, distribution and archival systems  Perform cGMP audit of R&D facilities and operations. Assist the team in auditing contract manufacturers / vendors / contract testing laboratory.  Coordinating in responding to all customer queries / audit findings related to R&D department. Institutionalize a system and track timely closure of CAPAs and audit findings  Ensure R&D team practices, systems and documentation are in compliance with respect to data integrity norms.  Implement systems for Change Control and Lab investigations in R&D.  Ensure R&D team is trained for their relevant job function and GMP / GLP training.  To handle customer and regulatory audits.  Provide quality related inputs to new projects, existing project, up gradations etc.  Participate in identification of Key Starting Material (KSM) / Registered Starting Material (RSM) and ensure that it is correctly identified.  Participate in handling of Out of Specification, Out of Trends, Deviation, Batch failure, Rejections, investigations and CAPA implementation at site.  Establish raw material standards by studying manufacturing / R&D requirements -conferring with suppliers.

Qualification & Experience                                 Qualifications for Full-Time HealthCare Aide: . 0-5yrs experience.                              

Qualification & Experience       Qualification:- GNM/BSc- Nursing          Experience:- 0 to 10 Years    

Qualification & Experience           Experience : 1 Year and above            Place : Calicut              Description : B Pharm or D Pharm 

Qualification & Experience                                 Qualifications for Full- Time Manager - Operations: . Post Graduate in Hospital ManagementExperience: · 8-10 yrs                      

ResponsibilitiesTo receive, sort and check soiled / contaminated instruments, containers, treatment trays and other supplies and equipment that have been used in the operation theater, ICU, wards, emergency (casualty) room and Catheterization Labarotory and prioritize disinfection and sterilization depending on emergency requisitions. To carry out preliminary check of supplies, i.e. check the functionality of reusable items that need to be sterilized. To inspect and replace missing or damaged equipment, make minor repairs on them, maintain inventory of supplies to include documenting usage, issuing, receiving and reordering as assigned. To carry out manual cleaning and / or cleaning by machines of the reprocessible items received after being used for patient treatment and care. To operate automatic and semi-automatic sterilizing equipments like steam sterilizers, Ethylene oxide sterilizers, Ultrasonic cleaners To accurately compute the sterilization process for all items using the method determined by the manufacturer and Infection control. To maintain an accurate record regarding the effectiveness of the various processes of cleaning, disinfections and sterilization. To ensure all user departments receive supplies of sterile instruments, linen and dressing material in adequate quantities and whenever required. To maintain high standard of environmental cleanliness. To ensure care and maintenance of all equipment in department. To maintain Quality Control parameters for all methods of sterilization and to document the effectiveness of each method. To perform other related duties incidental to work described as assigned. To actively participate in internal / external training programs. Escalate in case of major problems in equipment / provision of supplies / other process related major events. Develop and maintains standards of Processes to be carried out in the department. Ensure optimum utilization of resources and quality assurance in service delivery. Ensure interdepartmental communication is clear and effective. Prepare monthly duty rota whenever assigned & ensure shifts are adequately manned, report absenteeism. Collaborate with all the Nursing Units and other service areas departments for any change in their requirement of sterile instruments, linen packs and dressings. Assist in Training and Competency assessment of new joinees. Provide inputs for training needs of staff to Incharge. Provide inputs for performance review of staff, if required by Incharge. Review current SOPs to update any changes in processes. Inventory management of Department supplies. Allocate duties to the team members as per requirement. Supervise completion of documentation. Resolution of day-to-day operational issues. Quality improvement implementation.

Qualification & Experience                                 Qualifications for Full-Time Consultants: . MD/MS with a minimum of 5 years of experience.Retiring HODs and Senior Registrars looking for full time roles are also encouraged to apply.Qualifications for Senior Registrars: . MD/MS with a minimum of 2 years of experience.

Qualification & Experience      Qualification: Certificate (MT)    Experience: 1 – 5 years            Open for rotation shifts (24*7)              

ResponsibilitiesClinical Duties Assess, diagnose, and manage patients with hematological and oncological conditions. Perform detailed patient history taking and clinical examinations. Participate in daily ward rounds with consultants. Initiate and monitor treatment plans, including chemotherapy protocols. Manage oncological emergencies such as: Febrile neutropenia Tumor lysis syndrome Hypercalcemia Monitor patient progress and modify treatment plans accordingly. Procedural Responsibilities Perform basic procedures such as: Venipuncture Central line care (as per training) Bone marrow aspiration/biopsy (if trained) Assist in advanced hematology/oncology procedures when required. Inpatient & Outpatient Care Manage admitted patients and ensure continuity of care. Support outpatient clinics under consultant supervision. Coordinate admissions, discharges, and referrals. Documentation & Compliance Maintain accurate and up-to-date medical records. Document treatment plans, progress notes, and discharge summaries. Ensure adherence to hospital protocols, NABH/JCI standards. Multidisciplinary Coordination Work closely with: Medical oncologists Radiation oncologists Pathologists Nursing staff Participate in tumor boards and case discussions. Academic & Training Attend CMEs, academic sessions, and departmental meetings. Participate in clinical audits and research activities. Keep updated with latest protocols in haemato-oncology. Qualification & Experience     MBBS with KMC registration Experience in Haematology/Oncology is an advantage Skills Required Strong clinical assessment and decision-making skills Knowledge of chemotherapy protocols Ability to handle critical and emergency cases Good communication and teamwork skills Experience 0–3 years (or as per hospital requirement) Prior exposure to oncology/hematology preferred