1870 Safety Jobs - Page 20

Hetero Drugs Limited is looking for WAREHOUSE JUNIOR OFFICER HLL-IIIA to join our dynamic team and embark on a rewarding career journey Oversee warehouse operations and activities. Manage inventory and storage systems. Coordinate receiving, storage, and distribution of goods. Monitor and report on warehouse performance. Ensure compliance with safety and operational standards. Maintain warehouse records and documentation. Selected Candidate need to work in Warehouse Department. Qualification : B.Sc B.Com with Computer Knowledge Skills : Good Knowledge in Computer Skills.

1. Monitoringof Site Activities 2. FindingUnsafe Acts Unsafe conditions and escalating the same to plant HSE leadclearing the same on shop floor by the deviated departments. 3. Supportingto plant HSE Lead in the HSE functions/ activities/ procedures in relateddocumentations as per the department requirements. 4. Ensuringto impart the Tool Box Talks to workmen or conducting by the supervisors priorto the work activities. 5. Updatingthe HSE documentation on regular basis. 6. Ensuringthe contractors workmen to follow the HSE policies procedures as per theHetero Plasma Sciences Pvt Ltd. 7. Monitoringthe vendors/ contractors at site during execution of works and their sitevisits. 8. Regularsite inspections/ site rounds. 9. Ensuringto monitor the activities whether they (Hetero team/ contractor workmen) areadhering to work permits or not and raising the deviation as per the violation. 10. Planningdoing the HSE activities at site as per the HSE planner by coordinatingwith cross functional departments. 11. Periodicchecking inspection of Safety Emergency equipments and clearing its gapsif there will any by the support of concerned departments.

1.To involve in plasma products manufacturing. 2.Follow shift and production schedules. 3.To complete the assigned trainings timely. 4.To Monitor the differential pressure, temperature and humidity of the classified area. 5.To Ensure the area, equipments cleaning and readiness of equipments for batch activity. 6.Preparation of buffers and other solutions for downstream process. 7.Handling of process related instruments and equipments in downstream process (DSP). 8.Perform all the assigned manufacturing activities as per the defined procedures (SOP, BMR, Protocols) and record the details in respective document. 9.Checking the availability of stock of chemicals, solvents, raw material etc. 10.Coordinate with cross functional teams for smooth batch operations. 11.To maintain the facility to compliance with GMP. 12.Responsible for execution of relevant documents as per GDP. 13.To involve in equipment qualification and validation of the downstream equipments. 14.To involve in execution of process validation batches and regular manufacturing batches. 15.Provide samples to QC and take follow up for QC testing result. 16.In case of any abnormalities/ deviation observed should be recorded and informed to process in-charge to avoid any quality issues in the product. 17.To ensure adherence to safety procedure and report unsafe conditions and incidents to Supervisor. 18.To Involve in the preparation of SOPs and QMS documents. 19. To involve in new facility layout, equipment commissioning (URS, DQ, DS, FAT and SAT) documents preparation / review

Responsible for following activities in purification area of BM/BU based on campaign basis 1. Following GMP, safety practices in production facilities and work place. 2. Responsible for production activities: Execution of area, line clearance before execution of activities. Execution of product changeover activities. Responsible for column cleaning, packing, unpacking, evaluation and maintenance. Responsible for drug substance (FDS) transfer/dispensing. Execution of production activities. Monitoring and review of batch parameters/performance. Ensuring material are arranged properly before activities. Verification of samples for analysis. Responsible for shift Monitoring. Handling of online reject material. Review of soft copy for batch monitoring and performance. Execution of process validation. Execution of cleaning validation. Execution of verification protocols/equipment specific protocols. Ensuring buffer preparation in respective shift. 3. Handling of documents: Preparation of new / revision of SOPs, protocols and reports. Preparation of MFRs and BMR's. Primary review of executed BMR's submission to QA. Ensuring online BMR's updation and review of log books. 4. Responsible for monitoring and operation of following production equipments (but not limited to): AKTA Process Purification system Conductivity meter TFF System Peristaltic pumps Weighing Balance Mixing Systems Biosafety cabinet Filter integrity tester pH meter Walk in cold Freezer room Heat Exchanger Mixing vessels Ensuring proper data backup of equipments. Provide clearance for calibration, PMP and validation of equipments. Participate in execution of equipment validations. 5. Responsible for Quality Management Systems Initiation / Review of breakdown request. Initiation of CRN's and Preparation of Risk Assessments. Initiation of incidents, investigation, CAPA. 6. Team member: Facility readiness for audits. 7. Training: Training team members on SOPs / GMP aspects. Attending training on related SOP's / GMP aspects. 8. Monitoring of PM/Qualification of purification area equipments. (Calibration / PMP/Qualification).ease enter job description

1.To involve in plasma products manufacturing. 2.Follow shift and production schedules. 3.To complete the assigned trainings timely. 4.To Monitor the differential pressure, temperature and humidity of the classified area. 5.To Ensure the area, equipments cleaning and readiness of equipments for batch activity. 6.Preparation of buffers and other solutions for downstream process. 7.Handling of process related instruments and equipments in downstream process (DSP). 8.Perform all the assigned manufacturing activities as per the defined procedures (SOP, BMR, Protocols) and record the details in respective document. 9.Checking the availability of stock of chemicals, solvents, raw material etc. 10.Coordinate with cross functional teams for smooth batch operations. 11.To maintain the facility to compliance with GMP. 12.Responsible for execution of relevant documents as per GDP. 13.To involve in equipment qualification and validation of the downstream equipments. 14.To involve in execution of process validation batches and regular manufacturing batches. 15.Provide samples to QC and take follow up for QC testing result. 16.In case of any abnormalities/ deviation observed should be recorded and informed to process in-charge to avoid any quality issues in the product. 17.To ensure adherence to safety procedure and report unsafe conditions and incidents to Supervisor.

1. Follow shift schedule and production schedule as per process requirement. 2.Handling of plasma collection, sanitization, washing, cutting, pooling and thawing. 3.Handling of plasma fractionation process steps. 4.Compliance to all approved procedure, documents and GMP activities. 5.Performing all the assigned manufacturing activities in confirmation to BMR, protocols and recording the details in record sheets and logbooks. 6.In process samples sending to QC for analysis. 7.Performing COP, CIP, PHT and SIP of all the process vessels and equipment. 8.Performing calibration of pH, conductivity meters, turbidity meter, weighing balances and other equipment. 9.Preparation of buffers and other solutions for plasma fractionation process. 10.Monitoring of area cleaning, equipment surface sanitization, differential pressure, temperature and humidity 11.Monitoring and recording the temperature of freezer room and cold room. 12.To get involved in trouble shooting and managing day to day activities. 13.Checking the availability of stock of chemicals, solvents, raw material etc. 14.Report unsafe conditions and incidents to shift in-charge. 15.Adherence to safety procedures. 16.Awareness on PPE usage.

1.Follow shift schedule and production schedule as per process requirement. 2.Handling of Fractionation process steps like plasma bags collection, sanitization washing, plasma cutting, pooling thawing. 3.Performing COP of all the vessels and equipments in plasma fractionation area. 4.Perform all the assigned manufacturing activities as per the defined procedures (SOP, BMR, Protocols) and record the details in respective document. 5.Sending the In-process samples to QC for analysis. 6.Materials should be collected from warehouse and QC. 7.Helping of plasma fractionation process steps. 8.Performing cleaning, calibration and operation of pH, conductivity meters, turbidity meter, weighing balances and other equipments. 9.Preparation of buffers and other solutions for plasma fractionation process. 10.Ensure the monitoring and performing of area cleaning, equipments surface sanitization, pressure differentials, temperature and relative humidity. 11.Process waste collection from clean rooms and the same should be sent to scrap yard. 12.Garments and shoes should be arranged into the respective change rooms. 13.Assembling and dis-assembling of centrifuge and filter press equipments. 14.To ensure adherence to safety procedure and report unsafe conditions and incidents to Supervisor.

We are seeking skilled and proactive individuals for our Maintenance Department to ensure the smooth operation of production equipment, utilities, and infrastructure, minimizing downtime and maximizing efficiency. Key Responsibilities: Learn and assist in performing preventive and corrective maintenance on production machinery and utility systems, including reactors, centrifuges, dryers, compressors, HVAC systems, boilers, and chillers. Support troubleshooting and resolving technical issues related to mechanical, electrical, and instrumentation systems. Participate in the calibration and validation of equipment and instruments to meet regulatory requirements. Assist in maintaining detailed maintenance logs, schedules, and related documentation. Ensure adherence to Good Engineering Practices (GEP) and follow safety protocols. Collaborate with production and quality teams to ensure equipment reliability and efficiency. Participate in the installation, commissioning, and qualification of new equipment. Qualifications: Education: Diploma / ITI in Fitter / Mechanical / Electrical / Chemical Experience: Freshers. Basic understanding of maintenance tools, equipment, and safety practices is an advantage. Key Skills: Eagerness to learn and adapt to a dynamic work environment. Strong technical aptitude and problem-solving abilities. Effective communication and teamwork skills. Willingness to work in shifts and under supervision.

1. Follow SOPs, GMP and safety practices. 2. Facility Area cleaning, Equipment cleaning, drains cleaning sanitization. 70 % IPA arrangement. Discarding general waste, rejects and biowaste. Log books updation. Spillage management. Updating of BMRs and annexures online. 3. Material Arrangement of plastic / glassware. Material packing for sterilization. Arrangement of garments. Arrangement of materials. 4. Process Arrangement of drums and installation of bags. Collection of WFI. Movement of prepared media/buffer to process rooms. Assisting in cleaning of equipments. Movement of samples. Execution of production activities. Monitoring of batch parameters. Arrangement of HDPE Drums, Vessels and installation of SUM bags and liner bags. Samples handling (Sampling and labelling). Handling of Depth filters assembly and harvest activities. Media Buffer preparation activities for process. LN2 container handling for filling activities. 5. Participate in training programs as per training schedule. 6. Responsible for operation of following production equipments (but not limited to): Mixing systems Weighing balance Magnetic stirrer Peristaltic pumps pH meter Cold Room Freezer Heat exchanger Depth filter holders Laminar air flow cabinet Biosafety cabinet Pass box LN2 container

1. Following GMP, safety practices in production facilities and work place. 2. Responsible for buffer preparation activities Area drains cleaning and documents updation. Verification and receiving of material required for buffer preparation activities. Execution of Buffer preparation activities. Preparation of area, equipments before batch activities. Updation of batch parameters. Samples handling (Sampling and labelling). Intimation of incidents to Shift in-charge. Updation of room / equipment status labels. Arrangement of sterile material. 3. Handling of documents Updation of log books. Updation of BMRs and protocols/reports 4. Responsible for operation of following production equipments Mixing systems Conductivity meter Weighing balance Peristaltic pumps Walk in Cold room Freezer room Magnetic Stirrer pH meter Heat exchanger 5. Attending training on SOP's / GMP as per schedule

To Plan Monitor work force in labelling packing. To ensure business orders are executed on time as per customer requirement. To ensue SAP compliance. To Plan Monitor work force in Visual inspection. To ensure visual inspectors are in qualified state. To ensure all drug products movement in Cold room with safe systematic approach. To identify/perform/review QMS related activities in Packing and visual inspection. To ensure all quality systems are in place before product process activity. To handle regulatory and non-regulatory audits as lead Role. To plan Trainings, improvements, Stress management, Feedback Mechanism ,Skill test ,Outing etc. for Team members. To identify/evaluate/Implement the exact requirement with respect to equipment/Manpower/new method/Safety by forecasting approach. Report to Reporting manager related to daily work/any hurdles.

1. Following GMP, safety practices in production facilities and work place. 2. Responsible for production activities: Monitoring of area drains cleaning and documents updation. Updation of area / equipment status labels. Samples handling (Sampling and labelling). Arrangement of material required for activities. Assisting in Execution of production activities. Updation of BMR's. Receiving material (RM miscellaneous). Returning miscellaneous materials to warehouse. Planning and Execution of FDS thawing and dispensing activities. Assisting in product changeover activities before batch execution. Assisting column packing and execution of equipment specific protocols. Assisting in Equipment (Purification TFF system) cleaning.

Cisro hospital is looking for RMO (Resident Medical Officer) to join our dynamic team and embark on a rewarding career journey Provide round-the-clock medical care to critically ill patients in the ICU, including initial assessment, diagnosis, and management under the supervision of consultants. Monitor patient progress by conducting daily rounds, reviewing charts, and adjusting treatment plans as necessary. Administer and supervise the use of life support systems such as ventilators, intravenous drips, and other critical medical equipment. Ensure timely execution of medical orders such as tests, medications, and procedures, while maintaining precise documentation of patient progress. Collaborate with multidisciplinary teams, including nurses, consultants, and specialists, to provide comprehensive patient care and ensure effective communication regarding treatment plans. Respond promptly to medical emergencies and changes in patient conditions, initiating appropriate interventions and coordinating advanced care as needed. Participate in patient handovers, ensuring thorough communication of critical information during shift changes. Guide and mentor junior doctors, providing supervision and support in handling complex cases. Engage in continuous learning and stay updated with the latest developments in critical care medicine to apply evidence-based practices in patient management. Maintain high standards of patient safety, infection control, and ethical care in compliance with hospital protocols and guidelines.

Jinkushal cardiac care & super speciality hospital is looking for ICU RMO (Resident Medical Officer) to join our dynamic team and embark on a rewarding career journey Provide round-the-clock medical care to critically ill patients in the ICU, including initial assessment, diagnosis, and management under the supervision of consultants. Monitor patient progress by conducting daily rounds, reviewing charts, and adjusting treatment plans as necessary. Administer and supervise the use of life support systems such as ventilators, intravenous drips, and other critical medical equipment. Ensure timely execution of medical orders such as tests, medications, and procedures, while maintaining precise documentation of patient progress. Collaborate with multidisciplinary teams, including nurses, consultants, and specialists, to provide comprehensive patient care and ensure effective communication regarding treatment plans. Respond promptly to medical emergencies and changes in patient conditions, initiating appropriate interventions and coordinating advanced care as needed. Participate in patient handovers, ensuring thorough communication of critical information during shift changes. Guide and mentor junior doctors, providing supervision and support in handling complex cases. Engage in continuous learning and stay updated with the latest developments in critical care medicine to apply evidence-based practices in patient management. Maintain high standards of patient safety, infection control, and ethical care in compliance with hospital protocols and guidelines.

We are seeking a meticulous and detail-oriented Quality Control Engineer with a degree in Mechanical Engineering to join our team. The ideal candidate will be responsible for ensuring the quality and reliability of our products through comprehensive inspection and testing procedures. This role requires a strong understanding of mechanical engineering principles, quality control standards, and an ability to collaborate effectively with cross-functional teams. Quality Control: Quality Assurance: Implement and maintain quality control procedures to ensure compliance with industry standards and customer requirements. Product Inspection: Perform thorough inspections of mechanical components, subassemblies, and finished products to identify defects, deviations, and non-conformities. Testing and Analysis : Conduct various tests and experiments to evaluate the performance, durability, and functionality of mechanical systems and components. Documentation: Prepare detailed reports and documentation of inspection findings, test results, and quality metrics. Maintain accurate records of quality control activities. Root Cause Analysis: Investigate quality issues and deviations to determine root causes and implement corrective actions to prevent recurrence. Process Improvement: Identify opportunities for process improvement and efficiency enhancement in manufacturing processes to optimize product quality and reliability. Supplier Quality Management: Collaborate with suppliers to ensure the quality of incoming materials and components, and address quality issues effectively. Cross-functional Collaboration : Work closely with design engineering, manufacturing, and supply chain teams to communicate quality requirements, resolve quality issues, and drive continuous improvement initiatives. Regulatory Compliance: Ensure compliance with relevant regulatory requirements and industry standards (e.g., ISO, ASTM) pertaining to product quality and safety. Proficiency in coordinating and facilitating third-party inspections, ensuring adherence to quality standards and specifications . Qualification: Diploma or BE in Mechanical Engineer

A Rig Superintendent oversees all drilling operations on a rig site, ensuring safety, efficiency, and compliance with regulations. They are responsible for personnel management, equipment maintenance, and adherence to drilling programs and company policies. They lead daily operations meetings, conduct risk assessments, and promote a strong safety culture. Here's a more detailed breakdown of their responsibilities: Key Responsibilities: Supervision and Leadership: Directs all rig site activities including drilling, well completion, and workover operations. Leads daily operations meetings and safety briefings. Supervises and manages rig crews and service company personnel. Ensures personnel are aware of and follow all company policies and procedures. Promotes a positive and productive work environment.

Welders shall aware MIG/TIG with minimum 3 to 4 years of experience preferably in Heavy Industries, with ITI and NCVT. Should have knowledge of all types of welding positions. Should have knowledge and awareness how to read RT joint film and to rectify the joint in case of any discontinuity. Should have knowledge and awareness how to rectify the welding defects. Should have knowledge and awareness of weld defects and their remedial measures. Ability of reading the drawing of bogies & components for painting. Read and implement masking plans. Assistance when preparing bogies and components. Mixing paints and primers. Operate and monitor the paint pump and conveying systems, as well as the spray guns. Order the daily quantity of required paints for the paint warehouse. Taking masking film off bogies and components. Painting of bogies and components. Controlling bogies and components on and off exhaust m/c working. Recording test values and adherence in test reports. Specification of the required drying times. Awareness of safety policy. Awareness of PPE uses. Awareness of Emergency response at site. Awareness of Safe use of equipment's. Basic skills for safe work culture. Knowledge of Hazards identified. Knowledge of safety related improvement. Knowledge of crane operation working experience in industry. Knowledge of quality requirements after painting DFT checking visual inspection & adhesion test. Desired Skills: You should have minimum experience of 2 years and ITI (Painting General Trade) +NCVT passed in painting industries. An interest of learning, ability to work in team, analytical ability.

Aster Medcity is looking for Trainee Technician Laboratory to join our dynamic team and embark on a rewarding career journey Training and Learning: Participate in on-the-job training to learn laboratory procedures, safety protocols, and relevant scientific principles Sample Handling: Assist in the collection, preparation, labeling, and storage of laboratory samples, ensuring accuracy and compliance with established protocols Equipment Operation: Learn to operate and maintain laboratory equipment, such as microscopes, spectrophotometers, centrifuges, and pipettes, following standard procedures Data Recording: Accurately record experimental data, measurements, and observations in laboratory notebooks or electronic systems Quality Control: Assist with quality control procedures, including calibration and maintenance of equipment, to ensure accurate and reliable results Safety Compliance: Follow safety guidelines and laboratory protocols to maintain a safe working environment for oneself and colleagues Sample Testing: Assist with sample testing, experiments, or analysis as directed by senior laboratory staff Inventory Management: Help maintain laboratory supplies, chemicals, and equipment inventory, and assist in reordering supplies as needed Laboratory Cleanup: Participate in laboratory cleaning, waste disposal, and general maintenance to ensure a clean and organized workspace Compliance: Adhere to laboratory regulations, safety standards, and quality control procedures Reporting: Communicate findings, results, and issues to senior laboratory staff as required Problem-Solving: Assist in troubleshooting and resolving basic laboratory equipment and procedure issues under supervision

Aster Medcity is looking for Trainee Technician Laboratory to join our dynamic team and embark on a rewarding career journey Training and Learning: Participate in on-the-job training to learn laboratory procedures, safety protocols, and relevant scientific principles Sample Handling: Assist in the collection, preparation, labeling, and storage of laboratory samples, ensuring accuracy and compliance with established protocols Equipment Operation: Learn to operate and maintain laboratory equipment, such as microscopes, spectrophotometers, centrifuges, and pipettes, following standard procedures Data Recording: Accurately record experimental data, measurements, and observations in laboratory notebooks or electronic systems Quality Control: Assist with quality control procedures, including calibration and maintenance of equipment, to ensure accurate and reliable results Safety Compliance: Follow safety guidelines and laboratory protocols to maintain a safe working environment for oneself and colleagues Sample Testing: Assist with sample testing, experiments, or analysis as directed by senior laboratory staff Inventory Management: Help maintain laboratory supplies, chemicals, and equipment inventory, and assist in reordering supplies as needed Laboratory Cleanup: Participate in laboratory cleaning, waste disposal, and general maintenance to ensure a clean and organized workspace Compliance: Adhere to laboratory regulations, safety standards, and quality control procedures Reporting: Communicate findings, results, and issues to senior laboratory staff as required Problem-Solving: Assist in troubleshooting and resolving basic laboratory equipment and procedure issues under supervision

Aster Medcity is looking for Trainee Technician Laboratory to join our dynamic team and embark on a rewarding career journey Training and Learning: Participate in on-the-job training to learn laboratory procedures, safety protocols, and relevant scientific principles Sample Handling: Assist in the collection, preparation, labeling, and storage of laboratory samples, ensuring accuracy and compliance with established protocols Equipment Operation: Learn to operate and maintain laboratory equipment, such as microscopes, spectrophotometers, centrifuges, and pipettes, following standard procedures Data Recording: Accurately record experimental data, measurements, and observations in laboratory notebooks or electronic systems Quality Control: Assist with quality control procedures, including calibration and maintenance of equipment, to ensure accurate and reliable results Safety Compliance: Follow safety guidelines and laboratory protocols to maintain a safe working environment for oneself and colleagues Sample Testing: Assist with sample testing, experiments, or analysis as directed by senior laboratory staff Inventory Management: Help maintain laboratory supplies, chemicals, and equipment inventory, and assist in reordering supplies as needed Laboratory Cleanup: Participate in laboratory cleaning, waste disposal, and general maintenance to ensure a clean and organized workspace Compliance: Adhere to laboratory regulations, safety standards, and quality control procedures Reporting: Communicate findings, results, and issues to senior laboratory staff as required Problem-Solving: Assist in troubleshooting and resolving basic laboratory equipment and procedure issues under supervision

Aster Medcity is looking for Trainee Technician Laboratory to join our dynamic team and embark on a rewarding career journey Training and Learning: Participate in on-the-job training to learn laboratory procedures, safety protocols, and relevant scientific principles Sample Handling: Assist in the collection, preparation, labeling, and storage of laboratory samples, ensuring accuracy and compliance with established protocols Equipment Operation: Learn to operate and maintain laboratory equipment, such as microscopes, spectrophotometers, centrifuges, and pipettes, following standard procedures Data Recording: Accurately record experimental data, measurements, and observations in laboratory notebooks or electronic systems Quality Control: Assist with quality control procedures, including calibration and maintenance of equipment, to ensure accurate and reliable results Safety Compliance: Follow safety guidelines and laboratory protocols to maintain a safe working environment for oneself and colleagues Sample Testing: Assist with sample testing, experiments, or analysis as directed by senior laboratory staff Inventory Management: Help maintain laboratory supplies, chemicals, and equipment inventory, and assist in reordering supplies as needed Laboratory Cleanup: Participate in laboratory cleaning, waste disposal, and general maintenance to ensure a clean and organized workspace Compliance: Adhere to laboratory regulations, safety standards, and quality control procedures Reporting: Communicate findings, results, and issues to senior laboratory staff as required Problem-Solving: Assist in troubleshooting and resolving basic laboratory equipment and procedure issues under supervision

Aster Medcity is looking for Trainee Technician Laboratory to join our dynamic team and embark on a rewarding career journey Training and Learning: Participate in on-the-job training to learn laboratory procedures, safety protocols, and relevant scientific principles Sample Handling: Assist in the collection, preparation, labeling, and storage of laboratory samples, ensuring accuracy and compliance with established protocols Equipment Operation: Learn to operate and maintain laboratory equipment, such as microscopes, spectrophotometers, centrifuges, and pipettes, following standard procedures Data Recording: Accurately record experimental data, measurements, and observations in laboratory notebooks or electronic systems Quality Control: Assist with quality control procedures, including calibration and maintenance of equipment, to ensure accurate and reliable results Safety Compliance: Follow safety guidelines and laboratory protocols to maintain a safe working environment for oneself and colleagues Sample Testing: Assist with sample testing, experiments, or analysis as directed by senior laboratory staff Inventory Management: Help maintain laboratory supplies, chemicals, and equipment inventory, and assist in reordering supplies as needed Laboratory Cleanup: Participate in laboratory cleaning, waste disposal, and general maintenance to ensure a clean and organized workspace Compliance: Adhere to laboratory regulations, safety standards, and quality control procedures Reporting: Communicate findings, results, and issues to senior laboratory staff as required Problem-Solving: Assist in troubleshooting and resolving basic laboratory equipment and procedure issues under supervision

Job description Reviewing and evaluating adverse event reports to determine if they meet regulatory reporting requirements. Entering and maintaining adverse event information in safety databases Narrative writing Communicating with healthcare professionals and other stakeholders to gather additional information about adverse events Assisting in the preparation of safety reports to be submitted to regulatory agencies Monitoring safety literature to stay current on the latest safety information related to the products Collaborating with other departments such as clinical research, regulatory affairs, and pharma covigilance to ensure compliance with safety regulations and guidelines Participating in the development and implementation of safety policies and procedures Reviewing and assessing the safety profile of new and existing products Participating in the development and execution of risk management plans Communicating with regulatory authorities, healthcare professionals, and other stakeholders on safety-related issues.

We are searching for a skilled heavy equipment operator to utilize our industrial gear. The heavy equipment operator's duties include preparing and manipulating heavy equipment to ensure the appropriate movement of materials, and liaising with coworkers to ensure that the projects are completed accurately. You will be required to conduct your duties in a safe, diligent manner at all times. To ensure success as a heavy equipment operator, you should monitor workflow, suggesting alterations to enhance productivity, as needed. A remarkable heavy equipment operator will be attuned to the subtleties of each situation, possessing sound knowledge of when to lead or follow. Heavy Equipment Operator Responsibilities: Maneuvering motorized heavy equipment to ensure the accurate removal and placement of materials. Loading and offloading rocks, debris, and other materials from heavy equipment. Observing stipulated safety codes at all times. Communicating with coworkers to elucidate project specifications, as needed. Reporting injuries and other accidents to the line manager. Advising the line manager of requisite upgrades, repairs, and replacements.

As a Flow Wrap Machine Operator in the Food Processing Noodles Manufacturing industry at Kumbalagodu, Bangalore, you will be responsible for setting up, operating, and maintaining flow wrapping machines to pack noodles into sealed pouches or packets. Your role involves ensuring efficient packaging operations while upholding food safety, product quality, and equipment standards. Your key responsibilities will include setting up and operating flow wrap machines according to production schedules, loading packaging materials and noodle packs onto the machine, adjusting machine settings for product type and specifications, monitoring machine performance and output, checking packaging quality, and ensuring compliance with quality standards and food safety protocols. Additionally, you will be required to perform routine cleaning and minor maintenance on the machine, identify and resolve mechanical issues or escalate them to maintenance staff, maintain accurate production records, report any deviations to the shift supervisor, follow compliance with safety and hygiene standards, wear appropriate PPE, and keep the work area clean and organized. To excel in this role, you should have a minimum of 10th pass qualification with ITI/Diploma in Mechanical/Electrical being a plus, 1-3 years of experience operating flow wrap machines in a food manufacturing setting, basic mechanical knowledge of packaging machinery, the ability to read and follow SOPs and production schedules, attention to detail, problem-solving skills, and a safety-first mindset. The work environment will be a fast-paced, temperature-controlled food production facility where you may need to stand for long periods, operate machinery in rotating shifts, and handle lifting and moving materials up to 25 kg.,