Responsibilities: * Greet guests, manage front desk operations, maintain front office organization. * Answer phones, direct calls, provide exceptional customer service. *Looking for a confident individual with strong communication skills.
Responsibilities: Conduct medical monitoring, screening, and clinical exams. Oversee dosing, phlebotomy, and sample collection. Handle AEs, SAEs, emergencies, and ICU care. Supervise study activities, ICF, training, and data review. Health insurance Provident fund
Responsible for LC-MS/MS operations, method development, validation, GLP documentation, equipment calibration, and overall lab supervision, ensuring trained staff, smooth workflows, and timely, compliant bioanalytical project execution. Life insurance Job/soft skill training
To Operate, loading samples, create, quantify and save the batches as per LCMS/MS SOP. To complete necessary documentation for bio-analysis such as raw data forms and log book entries. To ensure that Bioanalytical method development and validation activity is progressing smoothly. To ensure that all the equipment and instruments in bioanalytical lab are appropriately qualified, calibrated and validated in line with SOP. To ensure that employees in the department are trained and up to date on all aspects related to bioanalytical systems and procedures and their record are maintained up to date. Ensure that records and data of bioanalytical equipment, processes and systems is up to date and in line with GLP requirements. Supervision of lab and contingency arrangements, project allocation and management of projects. Designating different activities to personnel. Design, implement and review all relevant SOP’s, protocol and report to be in line with current regulatory requirements. Responsible for overseeing of study timelines, activities and timely communication with management representative about the progress of the ongoing projects Ensure staff technical standards are maintained, GLP and safety training is provided and training records are maintained. Job Type: Full-time Pay: ₹35,000.00 - ₹50,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person
Role & responsibilities To Operate, loading samples, create, quantify and save the batches as per LCMS/MS SOP. To complete necessary documentation for bio-analysis such as raw data forms and logbook entries. To ensure that Bioanalytical method development and validation activity is progressing smoothly. To ensure that all the equipment and instruments in bioanalytical lab are appropriately qualified, calibrated and validated in line with SOP. To ensure that employees in the department are trained and up to date on all aspects related to bioanalytical systems and procedures and their record are maintained up to date. Ensure that records and data of bioanalytical equipment, processes and systems is up to date and in line with GLP requirements. Supervision of lab and contingency arrangements, project allocation and management of projects. Designating different activities to personnel. Design, implement and review all relevant SOPs, protocol and report to be in line with current regulatory requirements. Responsible for overseeing of study timelines, activities and timely communication with management representative about the progress of the ongoing projects Ensure staff technical standards are maintained, GLP and safety training is provided, and training records are maintained.
Role & responsibilities QMS role Preparation and overview of audit plan and conduct audits (In- process audit and retrospective audits) for clinical studies. Perform Retrospective audit of completed clinical study data including ICF, Individual CRF, Scanned CRF, TMF, eCTD and other relevant project specific documents etc. Quality review of Clinical study reports, Randomization schedule, study updates, ICD, screening records, etc. Preparation, issuance of audit reports. Prepare and review of SOP Compliance and verification of study audit response and closure of audit reports. Review Draft ICF, CRF, protocol and related documents before IEC approval. Planning and conducting of system audit and vendor audits. Requisition & Issuance of documents. Review equipment/instrument calibration record, IQ/OQ/PQ report. Provide training to new recruits in QA department. Any other task assigned by the Management.
Role & responsibilities To Operate, loading samples, create, quantify and save the batches as per LCMS/MS SOP. To complete necessary documentation for bio-analysis such as raw data forms and logbook entries. To ensure that Bioanalytical method development and validation activity is progressing smoothly. To ensure that all the equipment and instruments in bioanalytical lab are appropriately qualified, calibrated and validated in line with SOP. To ensure that employees in the department are trained and up to date on all aspects related to bioanalytical systems and procedures and their record are maintained up to date. Ensure that records and data of bioanalytical equipment, processes and systems is up to date and in line with GLP requirements. Supervision of lab and contingency arrangements, project allocation and management of projects. Designating different activities to personnel. Design, implement and review all relevant SOPs, protocol and report to be in line with current regulatory requirements. Responsible for overseeing of study timelines, activities and timely communication with management representative about the progress of the ongoing projects Ensure staff technical standards are maintained, GLP and safety training is provided, and training records are maintained.
Responsibilities: Secure and maintain study documents. Control and track access to files/archives. Retrieve records for audits/inspections. Archive and dispose of documents per SOPs/GCP. Ensure proper storage conditions and compliance. Over time allowance Health insurance Provident fund