Job Summary: The ETO (Ethylene Oxide) Machine Operator is responsible for the safe, effective, and compliant operation of Ethylene Oxide sterilization equipment used to sterilize medical devices. This role ensures that all sterilization processes follow established protocols, meet regulatory requirements and support timely production and distribution. Skills: · Operate ETO sterilization chambers and associated equipment according to Standard Operating Procedures (SOPs). · Load and unload medical devices into sterilization chambers in compliance with safety and sterility standards. · Monitor and record critical sterilization parameters (temperature, pressure, humidity, gas concentration, exposure time, etc.). · Ensure proper labelling and segregation of sterile and non-sterile products. · Maintain accurate batch records and logbooks for traceability and regulatory compliance. · Perform routine equipment checks, calibrations, and preventive maintenance. · Identify and escalate equipment malfunctions or deviations from standard processes. · Assist with validation runs and qualification protocols as needed (IQ/OQ/PQ). · Adhere to safety guidelines, including handling of hazardous materials and use of PPE. · Collaborate with Quality Assurance and Production teams to ensure product quality and regulatory compliance. Qualifications & Requirements: · High school diploma or equivalent; technical training or diploma in mechanical/electrical field preferred. · 1–3 years of experience operating ETo sterilization equipment, preferably in a medical device or pharmaceutical manufacturing environment. · Understanding of sterilization validation, biological indicators, and relevant quality standards. · Ability to read technical manuals, SOPs, and safety data sheets. · Comfortable working in controlled and regulated environments. · Strong attention to detail, documentation skills, and safety mindset. Working Conditions: · Standard working hours [9:00 AM – 6:00 PM] · Potential for overtime based on production demands. Job Type: Full-time Pay: ₹15,000.00 - ₹35,958.09 per month Schedule: Day shift Work Location: In person

Job Summary: The ETO (Ethylene Oxide) Machine Operator is responsible for the safe, effective, and compliant operation of Ethylene Oxide sterilization equipment used to sterilize medical devices. This role ensures that all sterilization processes follow established protocols, meet regulatory requirements and support timely production and distribution. Skills: · Operate ETO sterilization chambers and associated equipment according to Standard Operating Procedures (SOPs). · Load and unload medical devices into sterilization chambers in compliance with safety and sterility standards. · Monitor and record critical sterilization parameters (temperature, pressure, humidity, gas concentration, exposure time, etc.). · Ensure proper labelling and segregation of sterile and non-sterile products. · Maintain accurate batch records and logbooks for traceability and regulatory compliance. · Perform routine equipment checks, calibrations, and preventive maintenance. · Identify and escalate equipment malfunctions or deviations from standard processes. · Assist with validation runs and qualification protocols as needed (IQ/OQ/PQ). · Adhere to safety guidelines, including handling of hazardous materials and use of PPE. · Collaborate with Quality Assurance and Production teams to ensure product quality and regulatory compliance. Qualifications & Requirements: · High school diploma or equivalent; technical training or diploma in mechanical/electrical field preferred. · 1–3 years of experience operating ETo sterilization equipment, preferably in a medical device or pharmaceutical manufacturing environment. · Understanding of sterilization validation, biological indicators, and relevant quality standards. · Ability to read technical manuals, SOPs, and safety data sheets. · Comfortable working in controlled and regulated environments. · Strong attention to detail, documentation skills, and safety mindset. Working Conditions: · Standard working hours [9:00 AM – 6:00 PM] · Potential for overtime based on production demands. Job Type: Full-time Pay: ₹15,000.00 - ₹35,958.09 per month Schedule: Day shift Work Location: In person

Job Summary: Monitor trends in microbiological data and report deviations and out-of-specification results. Maintain, calibrate, and validate laboratory equipment according to SOPs. Review and approve microbiology-related documentation including SOPs, protocols, and test records. Assist in investigations for non-conformances and microbiological out-of-specification results. Participate in internal audits and support external audits and inspections. Maintain good documentation practices and ensure data integrity. Skills: · Oversee and maintain the Quality Management System (QMS) in accordance with ISO 13485, 21 CFR Part 820, and other applicable regulatory standards. · Lead and manage the QA team, including quality engineers, document control, and quality auditors. · Ensure effective implementation of CAPA, non-conformance (NC), change control, deviation, and risk management systems. · Support sterilization validation, equipment qualification, and product validation/verification processes. · Manage internal and external audits, including FDA inspections, ISO audits, and customer audits. · Develop, implement, and monitor quality policies, procedures, and training programs. · Work cross-functionally with Manufacturing, R&D, Regulatory, and Supply Chain to ensure product quality throughout the lifecycle. · Lead quality review boards (QRB), management reviews, and continuous improvement initiatives. · Track and report key quality metrics (KPIs) to senior management. · Review and approve quality-related documentation including batch records, protocols, and test results. Qualifications & Requirements: · Bachelor’s or Master’s degree in Microbiology, Biology, or related life sciences field. · 2+ years of relevant QA microbiology experience in a medical device, pharmaceutical, or biotech manufacturing environment. · Familiarity with aseptic techniques, environmental monitoring, and microbiological testing methods. · Working knowledge of FDA 21 CFR Part 820, ISO 13485, and GMP requirements. Working Conditions: · Standard working hours [9:00 AM – 6:00 PM] · Potential for overtime based on production demands. Experience = Fresher Job Type: Full-time Pay: ₹15,000.00 - ₹46,448.54 per month Schedule: Day shift Work Location: In person

Job Summary: The ETO (Ethylene Oxide) Machine Operator is responsible for the safe, effective, and compliant operation of Ethylene Oxide sterilization equipment used to sterilize medical devices. This role ensures that all sterilization processes follow established protocols, meet regulatory requirements and support timely production and distribution. Skills: · Operate ETO sterilization chambers and associated equipment according to Standard Operating Procedures (SOPs). · Load and unload medical devices into sterilization chambers in compliance with safety and sterility standards. · Monitor and record critical sterilization parameters (temperature, pressure, humidity, gas concentration, exposure time, etc.). · Ensure proper labelling and segregation of sterile and non-sterile products. · Maintain accurate batch records and logbooks for traceability and regulatory compliance. · Perform routine equipment checks, calibrations, and preventive maintenance. · Identify and escalate equipment malfunctions or deviations from standard processes. · Assist with validation runs and qualification protocols as needed (IQ/OQ/PQ). · Adhere to safety guidelines, including handling of hazardous materials and use of PPE. · Collaborate with Quality Assurance and Production teams to ensure product quality and regulatory compliance. Qualifications & Requirements: · High school diploma or equivalent; technical training or diploma in mechanical/electrical field preferred. · 1–3 years of experience operating ETo sterilization equipment, preferably in a medical device or pharmaceutical manufacturing environment. · Understanding of sterilization validation, biological indicators, and relevant quality standards. · Ability to read technical manuals, SOPs, and safety data sheets. · Comfortable working in controlled and regulated environments. · Strong attention to detail, documentation skills, and safety mindset. Working Conditions: · Standard working hours [9:00 AM – 6:00 PM] · Potential for overtime based on production demands. Job Type: Full-time Pay: ₹15,000.00 - ₹30,000.00 per month Schedule: Day shift Work Location: In person

Job Summary: Monitor trends in microbiological data and report deviations and out-of-specification results. Maintain, calibrate, and validate laboratory equipment according to SOPs. Review and approve microbiology-related documentation including SOPs, protocols, and test records. Assist in investigations for non-conformances and microbiological out-of-specification results. Participate in internal audits and support external audits and inspections. Maintain good documentation practices and ensure data integrity. Skills: · Oversee and maintain the Quality Management System (QMS) in accordance with ISO 13485, 21 CFR Part 820, and other applicable regulatory standards. · Lead and manage the QA team, including quality engineers, document control, and quality auditors. · Ensure effective implementation of CAPA, non-conformance (NC), change control, deviation, and risk management systems. · Support sterilization validation, equipment qualification, and product validation/verification processes. · Manage internal and external audits, including FDA inspections, ISO audits, and customer audits. · Develop, implement, and monitor quality policies, procedures, and training programs. · Work cross-functionally with Manufacturing, R&D, Regulatory, and Supply Chain to ensure product quality throughout the lifecycle. · Lead quality review boards (QRB), management reviews, and continuous improvement initiatives. · Track and report key quality metrics (KPIs) to senior management. · Review and approve quality-related documentation including batch records, protocols, and test results. Qualifications & Requirements: · Bachelor’s or Master’s degree in Microbiology, Biology, or related life sciences field. · 2+ years of relevant QA microbiology experience in a medical device, pharmaceutical, or biotech manufacturing environment. · Familiarity with aseptic techniques, environmental monitoring, and microbiological testing methods. · Working knowledge of FDA 21 CFR Part 820, ISO 13485, and GMP requirements. Working Conditions: · Standard working hours [9:00 AM – 6:00 PM] · Potential for overtime based on production demands. Experience = Fresher Job Type: Full-time Pay: ₹15,000.00 - ₹46,448.54 per month Schedule: Day shift Work Location: In person

Dusons Medicare LLP is Medical Equipment Manufacturing Company. In Himmatnagar, Gujarat. We are looking Machine Operators (EXP :- Molding, Packing, Assembly) Experience = Fresher we are providing stipend also for 3 to 6 month internship. Job Type: Full-time Pay: ₹15,000.00 - ₹40,000.00 per month Schedule: Day shift Work Location: In person

Dusons Medicare LLP is Medical Equipment Manufacturing Company. In Himmatnagar, Gujarat. We are looking Machine Operators (EXP :- Molding, Packing, Assembly) Experience = Fresher we are providing stipend also for 3 to 6 month internship. Job Type: Full-time Pay: ₹15,000.00 - ₹40,000.00 per month Schedule: Day shift Work Location: In person

Job Summary: We are seeking a skilled and detail-oriented Machine Operator to run and maintain equipment used in the manufacturing of blood collection tubes . The ideal candidate will have experience working with automated production lines in a cleanroom or medical-grade environment and a strong commitment to quality and safety standards. Key Responsibilities: Set up, operate, and monitor blood collection tube manufacturing machines (injection molding, labeling, vacuum Job Type: Full-time Pay: ₹15,000.00 - ₹30,000.00 per month Schedule: Day shift Work Location: In person