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
Job Summary: We are seeking a detail-oriented and proactive Purchase Executive to join our medical equipment manufacturing team. The ideal candidate will be responsible for sourcing, negotiating, and procuring materials, components, and services required for production, ensuring timely delivery, compliance with quality standards, and cost-effectiveness Skills: Strong knowledge of medical-grade materials and components. Familiarity with ERP systems (e.g., SAP, Oracle, Tally). Excellent negotiation and communication skills. Attention to detail and strong organizational skills. Understanding of regulatory and quality standards (ISO 13485, CE, FDA, etc.) is a strong advantage. 2–5 years of experience in purchasing or supply chain within a medical device, healthcare, or precision manufacturing environment. Job Type: Full-time Pay: ₹50,000.00 - ₹70,000.00 per month Schedule: Day shift Work Location: In person
Job Summary: We are seeking a highly skilled and detail-oriented Senior Quality Assurance (QA) Specialist to join our team in a medical equipment manufacturing environment. The successful candidate will be responsible for ensuring compliance with applicable regulatory standards (FDA, ISO 13485, MDR, etc.), leading quality assurance activities across the product lifecycle, and supporting continuous improvement initiatives in both design and manufacturing processes. Key Responsibilities: Ensure compliance with FDA 21 CFR Part 820 , ISO 13485 , ISO 14971 , and EU MDR regulations. Lead and participate in internal, supplier, and regulatory audits. Develop, implement, and maintain QA procedures , work instructions, and quality systems documentation. Support product development teams with design control activities, including risk management, verification, and validation. Lead CAPA (Corrective and Preventive Action) processes and conduct thorough root cause analyses. Oversee Non-Conformance (NC) investigations and support disposition activities. Coordinate supplier quality management , including supplier evaluations, audits, and performance monitoring. Participate in quality review boards (QRBs) and change control processes. Provide QA support during manufacturing transfer and process validation (IQ/OQ/PQ). Monitor and analyze quality metrics , prepare reports, and identify trends for continuous improvement. Train and mentor junior QA staff and cross-functional teams on quality policies and best practices. Job Type: Full-time Pay: ₹30,000.00 - ₹60,000.00 per month Schedule: Day shift Work Location: In person
Company Description Arcedges Building India LLP is a leading provider of innovative Pre-Engineered Building (PEB) solutions for industries across India. With a focus on engineering excellence, quality commitment, and timely delivery, we offer custom-designed industrial structures that are cost-effective, durable, and sustainable. Our modern manufacturing plant in Gujarat supports our growing presence and successful project deliveries for leading companies in various industries. Role Description This is a full-time on-site role for a Quotation Engineer located in Ahmedabad. The Quotation Engineer will be responsible for preparing detailed quotations for PEB projects, liaising with clients to understand their requirements, conducting site visits for measurements, and collaborating with the design and project teams to ensure accurate and competitive bids. Skill Estimation & Costing Reading and Preparation of engineering drawings Carry Out Survey and investigation of the subject Property contract document preparation working out rates and values. report writing by giving necessary reasons and basis Qualifications Strong technical background in engineering or related field Experience in preparing detailed quotations or cost estimates Knowledge of Pre-Engineered Building (PEB) solutions and construction processes Excellent communication and interpersonal skills Ability to work effectively in a team environment Bachelor's degree in Engineering or a related field Previous experience in the construction or infrastructure industry is a plus Job Type: Full-time Pay: ₹30,000.00 - ₹50,000.00 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Schedule: Day shift Work Location: In person
Job Summary: We are seeking a skilled and detail-oriented Injection Moulding Machine Operator to join our team in a cleanroom medical equipment manufacturing facility. The operator will be responsible for setting up, operating, and maintaining injection moulding machines to produce high-quality plastic components used in medical devices, while adhering to strict regulatory and quality standards . Qualifications: High school diploma or equivalent required. Technical certification or vocational training in plastics processing or manufacturing preferred. Minimum 1–3 years of experience in injection moulding, preferably in a medical or regulated manufacturing environment. Familiarity with cleanroom practices and quality systems (ISO 13485, GMP). Ability to read and interpret technical drawings, work instructions, and inspection tools. Basic mechanical troubleshooting skills. Strong attention to detail and manual dexterity. Job Type: Full-time Pay: ₹15,000.00 - ₹50,000.00 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Schedule: Day shift Work Location: In person
Job Summary: We are seeking a skilled and detail-oriented Injection Moulding Machine Operator to join our team in a cleanroom medical equipment manufacturing facility. The operator will be responsible for setting up, operating, and maintaining injection moulding machines to produce high-quality plastic components used in medical devices, while adhering to strict regulatory and quality standards . Qualifications: High school diploma or equivalent required. Technical certification or vocational training in plastics processing or manufacturing preferred. Minimum 1–3 years of experience in injection moulding, preferably in a medical or regulated manufacturing environment. Familiarity with cleanroom practices and quality systems (ISO 13485, GMP). Ability to read and interpret technical drawings, work instructions, and inspection tools. Basic mechanical troubleshooting skills. Strong attention to detail and manual dexterity. Job Type: Full-time Pay: ₹15,000.00 - ₹50,000.00 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Schedule: Day shift Work Location: In person