An administrative role involves overseeing and managing daily office operations to ensure efficiency and effectiveness. Administrators are responsible for a wide range of tasks, including record-keeping, scheduling, communication, and office supply management. They often serve as a point of contact for both internal and external stakeholders, providing support and coordination. Key Responsibilities of an Administrator: Record Keeping and Data Management: Maintaining organized and up-to-date records, files, and databases. Scheduling and Coordination: Managing calendars, scheduling meetings, appointments, and travel arrangements. Communication and Correspondence: Handling incoming and outgoing correspondence, emails, and phone calls. Office Supply Management: Ordering, managing, and maintaining office supplies and equipment. Support for Other Departments: Assisting with tasks for HR, finance, and other departments. Data Entry and Reporting: Entering data into spreadsheets, reports, and databases. Meeting Organization: Preparing agendas, taking minutes, and arranging meeting venues. Event Coordination: Assisting with the planning and execution of office events and activities. Supervision and Training: In some cases, supervising other administrative staff and providing training. Compliance: Ensuring adherence to company policies and procedures, and relevant regulations. Job Type: Permanent Pay: ₹15,000.00 - ₹18,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person
An administrative role involves overseeing and managing daily office operations to ensure efficiency and effectiveness. Administrators are responsible for a wide range of tasks, including record-keeping, scheduling, communication, and office supply management. They often serve as a point of contact for both internal and external stakeholders, providing support and coordination. Key Responsibilities of an Administrator: Record Keeping and Data Management: Maintaining organized and up-to-date records, files, and databases. Scheduling and Coordination: Managing calendars, scheduling meetings, appointments, and travel arrangements. Communication and Correspondence: Handling incoming and outgoing correspondence, emails, and phone calls. Office Supply Management: Ordering, managing, and maintaining office supplies and equipment. Support for Other Departments: Assisting with tasks for HR, finance, and other departments. Data Entry and Reporting: Entering data into spreadsheets, reports, and databases. Meeting Organization: Preparing agendas, taking minutes, and arranging meeting venues. Event Coordination: Assisting with the planning and execution of office events and activities. Supervision and Training: In some cases, supervising other administrative staff and providing training. Compliance: Ensuring adherence to company policies and procedures, and relevant regulations. Job Type: Permanent Pay: ₹15,000.00 - ₹18,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person
An administrative role involves overseeing and managing daily office operations to ensure efficiency and effectiveness. Administrators are responsible for a wide range of tasks, including record-keeping, scheduling, communication, and office supply management. They often serve as a point of contact for both internal and external stakeholders, providing support and coordination. Key Responsibilities of an Administrator: Record Keeping and Data Management: Maintaining organized and up-to-date records, files, and databases. Scheduling and Coordination: Managing calendars, scheduling meetings, appointments, and travel arrangements. Communication and Correspondence: Handling incoming and outgoing correspondence, emails, and phone calls. Office Supply Management: Ordering, managing, and maintaining office supplies and equipment. Support for Other Departments: Assisting with tasks for HR, finance, and other departments. Data Entry and Reporting: Entering data into spreadsheets, reports, and databases. Meeting Organization: Preparing agendas, taking minutes, and arranging meeting venues. Event Coordination: Assisting with the planning and execution of office events and activities. Supervision and Training: In some cases, supervising other administrative staff and providing training. Compliance: Ensuring adherence to company policies and procedures, and relevant regulations. Job Type: Full-time Pay: ₹15,000.00 - ₹18,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person
An administrative role involves overseeing and managing daily office operations to ensure efficiency and effectiveness. Administrators are responsible for a wide range of tasks, including record-keeping, scheduling, communication, and office supply management. They often serve as a point of contact for both internal and external stakeholders, providing support and coordination. Key Responsibilities of an Administrator: Record Keeping and Data Management: Maintaining organized and up-to-date records, files, and databases. Scheduling and Coordination: Managing calendars, scheduling meetings, appointments, and travel arrangements. Communication and Correspondence: Handling incoming and outgoing correspondence, emails, and phone calls. Office Supply Management: Ordering, managing, and maintaining office supplies and equipment. Support for Other Departments: Assisting with tasks for HR, finance, and other departments. Data Entry and Reporting: Entering data into spreadsheets, reports, and databases. Meeting Organization: Preparing agendas, taking minutes, and arranging meeting venues. Event Coordination: Assisting with the planning and execution of office events and activities. Supervision and Training: In some cases, supervising other administrative staff and providing training. Compliance: Ensuring adherence to company policies and procedures, and relevant regulations. Job Type: Full-time Pay: ₹15,000.00 - ₹18,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person
Job Title: Assistant Quality Manager / Quality Engineer Experience: 2–5 Years Department: Quality Assurance / Quality Control Industry: Medical Devices / Pharma / Healthcare Standards: ISO 13485, QMS, Regulatory Compliance Job Responsibilities: Assist the Quality Manager in maintaining and improving the Quality Management System (QMS) as per ISO 13485 requirements. Prepare and update Standard Operating Procedures (SOPs), Work Instructions, and Quality Manual. Participate in internal audits , supplier audits, and external regulatory audits (e.g., ISO, FDA). Support CAPA (Corrective and Preventive Action) and non-conformance investigations. Monitor and ensure document control , calibration, validation, and traceability of processes and equipment. Conduct training and awareness programs on QMS and regulatory requirements. Assist in product quality inspections and manage deviations and change controls. Maintain risk management files as per ISO 14971 (if applicable). Coordinate with cross-functional teams (R&D, production, supply chain) to ensure compliance. Prepare and maintain quality reports, metrics, and audit findings. Key Skills Required: Strong understanding of ISO 13485 QMS principles. Knowledge of GMP, CAPA, NCR, RCA, Validation, Risk Management . Proficient in internal audit processes and documentation practices. Attention to detail and analytical thinking. Excellent communication and organizational skills. Job Type: Full-time Pay: ₹30,000.00 - ₹40,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person
Department: Engineering / New Product Development (NPD) Location: MAJiK Medical Solutions Pvt ltd , M46, Sultanpur Experience: FRESHER Education: Bachelor’s Degree in Mechanical / Biomedical / Industrial Engineering (Required) Job Summary: The NPD Manufacturing Engineer will be responsible for supporting the design, development, and transition of new medical device products from concept to manufacturing. This includes process design, validation, equipment specification, and continuous improvement for manufacturability, quality, and cost-effectiveness. Key Responsibilities: Collaborate with R&D and design teams to ensure designs are manufacturable. Develop, evaluate, and optimize manufacturing processes for new products. Support prototype development, design for manufacturability (DFM), and scalability to production. Create and update process documentation, work instructions, and validation protocols (IQ/OQ/PQ). Conduct feasibility studies and process capability assessments. Select and qualify tools, jigs, and fixtures for production. Assist in regulatory documentation and compliance (ISO 13485, FDA QSR). Train production staff and technicians on new processes and equipment. Support pilot builds and engineering builds. Ensure smooth handover from development to manufacturing. Skills & Competencies: Strong knowledge of NPD and manufacturing engineering principles. Experience with medical device development (preferred). Proficiency in CAD (SolidWorks, AutoCAD) and MS Office. Hands-on knowledge of validation (IQ/OQ/PQ) and process qualification. Good understanding of GMP, ISO 13485, and regulatory requirements. Problem-solving mindset and ability to work in cross-functional teams. Excellent verbal and written communication skills. Job Type: Full-time Pay: ₹16,000.00 - ₹20,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person
Job Title: Quality Manager (ISO 13485 – Medical Devices) Location: M46, Sultanpur(V),Telangana Experience: 5+ years in Medical Device Quality Management Industry: Medical Devices Employment Type: Full-time Salary: Based on interview performance Key Responsibilities: Ensure compliance with ISO 13485 , FDA 21 CFR Part 820, and other applicable medical device regulations. Develop, implement, and maintain the Quality Management System (QMS) . Lead internal and external quality audits and manage audit findings and CAPA processes. Monitor and analyze non-conformances , deviations, and implement corrective/preventive actions. Supervise document control , change control, and record retention activities. Review and approve validation protocols and reports (process, equipment, software). Coordinate with cross-functional teams for quality assurance during design, manufacturing, and distribution phases. Ensure supplier quality management , including audits and evaluations. Conduct training programs on quality system procedures and regulatory requirements. Manage management review meetings and ensure timely updates to leadership. Maintain records for complaints, returns, and adverse events as per regulatory standards. Qualifications: Bachelor's degree in Engineering, Life Sciences, or related field (Master's preferred). Minimum 5 years of experience in medical device quality assurance . Strong knowledge of ISO 13485 , QSR (21 CFR 820), and risk management per ISO 14971. Experience in leading audits (e.g., Notified Body, FDA). Proficient in CAPA, Root Cause Analysis, and FMEA . Excellent communication, leadership, and problem-solving skills. Preferred Certifications (not mandatory): Certified Quality Auditor (CQA) Lead Auditor – ISO 13485 Job Type: Permanent Benefits: Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person
Company Description MAJiK Medical Solutions Pvt. Ltd. is an ISO13485 certified company that offers top-quality custom medical device development and manufacturing solutions to the global medical device industry. Specializing in complex medical catheters, MAJiK operates in over 25,000 SFT ISO Class 7/8 cleanroom manufacturing space in India, and produces a wide variety of medical devices. MAJiK is a comprehensive source for medical device development with in-house capabilities such as R&D Prototype manufacturing, Design development and Testing facilities, product manufacturing including hydrophilic coating, packaging, and sterilization. The company is expanding with a new 70,000 Sqft facility, positioning itself as one of the largest reinforced tubing manufacturers and finished medical device development and manufacturing firm in India. Role Description This is a full-time on-site role located in Hyderabad for a Research and Development Product Manager. The Research and Development Product Manager will be responsible for overseeing the R&D of new and existing products, managing project timelines, customer interaction and collaborating with cross-functional teams to ensure product development processes are efficient and effective. Day-to-day tasks include conducting research to enhance product designs, analyzing data to improve product performance, and ensuring products meet regulatory standards. Qualifications Strong Analytical Skills and Research Design Development and prototype manufacturing Experience in Research and Development (R&D) and Product Development Knowledge in Risk Analysis of Medical Device Products Knowledge in Design Control Documentation for development of Medical Devices Proficient in Project Management and Team interaction Excellent problem-solving and critical-thinking abilities Ability to work collaboratively with cross-functional teams Knowledge in the medical device industry Bachelor’s degree in Mechanical Engineering or Biomedical Engineering, or related field
Job Overview: We are seeking a highly skilled and motivated Polymer Engineer/ Extrusion Engineer / Process Engineer to join our dynamic engineering team. The ideal candidate will have expertise in polymer science and engineering, with a strong ability to design, develop, and optimize polymer-based materials and processes. The role involves working closely with cross-functional teams to innovate and improve products across various industries, including automotive, medical, packaging, and consumer goods. Key Responsibilities: Polymer Material Design : Develop and select appropriate polymers and composites for specific applications based on performance, cost, and sustainability criteria. Design and test new polymer materials for extrusion applications. Work with production teams to scale new products. Analyze performance data and adjust formulations or processes. Stay updated on new polymer technologies and industry trends. Ensure compliance with safety and environmental standards Material Testing & Analysis : Perform mechanical, thermal, and chemical tests on polymers to ensure quality and compliance with industry standards. Process Development : Design and optimize polymer processing techniques (e.g., extrusion, injection molding, blow molding, etc.) to improve efficiency, reduce waste, and enhance material properties. R&D and Innovation : Collaborate in research and development efforts to innovate new polymer formulations, improve existing products, and explore new applications of polymer materials. Collaboration with Manufacturing : Work closely with manufacturing teams to ensure smooth transition from prototype to mass production, providing technical support and troubleshooting during scale-up processes. Quality Assurance : Implement quality control measures to ensure consistency and reliability of polymer materials and finished products. Documentation & Reporting : Prepare detailed technical reports, data sheets, and documentation for internal and external stakeholders. Regulatory Compliance : Stay current with industry regulations and ensure that polymer products meet required health, safety, and environmental standards. Qualifications: Education : Bachelor's or Master's degree in Polymer Engineering, Materials Science, Chemical Engineering, Industrial Engineering. Experience : At least 4-5 years of experience in polymer engineering or related industries. Experience in product development, material testing, and polymer processing is highly desirable. Technical Skills : Expertise in polymer chemistry and material properties, Extrusion Knowledge of polymer processing techniques (e.g., injection molding, extrusion, thermoforming). Familiarity with analytical techniques like spectroscopy, chromatography, and microscopy. Proficiency with engineering software (e.g., CAD, simulation tools). Soft Skills : Strong problem-solving and analytical skills. Excellent communication and collaboration abilities. Ability to work independently and as part of a team. Certifications : Relevant certifications in polymer technology or materials science are a plus. Preferred Skills: Experience with sustainable polymers, bio-based polymers, or biodegradable materials. Knowledge of ASTM, ISO, or other industry standards related to polymers. Previous experience in the medical, or packaging industries. Benefits: Competitive salary. Opportunities for professional development and career advancement. A dynamic and collaborative work environment. Job Type: Full-time Pay: ₹40,000.00 - ₹50,000.00 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Work Location: In person
Job Overview: We are seeking a highly skilled and motivated Polymer Engineer / Process Engineer to join our dynamic engineering team. The ideal candidate will have expertise in polymer science and engineering, with a strong ability to design, develop, and optimize polymer-based materials and processes. The role involves working closely with cross-functional teams to innovate and improve products across various industries, including automotive, medical, packaging, and consumer goods. Key Responsibilities: Polymer Material Design : Develop and select appropriate polymers and composites for specific applications based on performance, cost, and sustainability criteria. Design and test new polymer materials for extrusion applications. Work with production teams to scale new products. Analyze performance data and adjust formulations or processes. Stay updated on new polymer technologies and industry trends. Ensure compliance with safety and environmental standards Material Testing & Analysis : Perform mechanical, thermal, and chemical tests on polymers to ensure quality and compliance with industry standards. Process Development : Design and optimize polymer processing techniques (e.g., extrusion, injection molding, blow molding, etc.) to improve efficiency, reduce waste, and enhance material properties. R&D and Innovation : Collaborate in research and development efforts to innovate new polymer formulations, improve existing products, and explore new applications of polymer materials. Collaboration with Manufacturing : Work closely with manufacturing teams to ensure smooth transition from prototype to mass production, providing technical support and troubleshooting during scale-up processes. Quality Assurance : Implement quality control measures to ensure consistency and reliability of polymer materials and finished products. Documentation & Reporting : Prepare detailed technical reports, data sheets, and documentation for internal and external stakeholders. Regulatory Compliance : Stay current with industry regulations and ensure that polymer products meet required health, safety, and environmental standards. Qualifications: Education : Bachelor's or Master's degree in Polymer Engineering, Materials Science, Chemical Engineering, Industrial Engineering. Experience : At least 0-1 years of experience in polymer engineering or related industries. Experience in product development, material testing, and polymer processing is highly desirable. Technical Skills : Expertise in polymer chemistry and material properties, Extrusion Knowledge of polymer processing techniques (e.g., injection molding, extrusion, thermoforming). Familiarity with analytical techniques like spectroscopy, chromatography, and microscopy. Proficiency with engineering software (e.g., CAD, simulation tools). Soft Skills : Strong problem-solving and analytical skills. Excellent communication and collaboration abilities. Ability to work independently and as part of a team. Certifications : Relevant certifications in polymer technology or materials science are a plus. Preferred Skills: Experience with sustainable polymers, bio-based polymers, or biodegradable materials. Knowledge of ASTM, ISO, or other industry standards related to polymers. Previous experience in the medical, or packaging industries. Benefits: Competitive salary. Opportunities for professional development and career advancement. A dynamic and collaborative work environment. Job Type: Full-time Pay: ₹18,000.00 - ₹20,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person
Job Overview: We are seeking a highly skilled and motivated Polymer Engineer/ Extrusion Engineer / Process Engineer to join our dynamic engineering team. The ideal candidate will have expertise in polymer science and engineering, with a strong ability to design, develop, and optimize polymer-based materials and processes. The role involves working closely with cross-functional teams to innovate and improve products across various industries, including automotive, medical, packaging, and consumer goods. Key Responsibilities: Polymer Material Design : Develop and select appropriate polymers and composites for specific applications based on performance, cost, and sustainability criteria. Design and test new polymer materials for extrusion applications. Work with production teams to scale new products. Analyze performance data and adjust formulations or processes. Stay updated on new polymer technologies and industry trends. Ensure compliance with safety and environmental standards Material Testing & Analysis : Perform mechanical, thermal, and chemical tests on polymers to ensure quality and compliance with industry standards. Process Development : Design and optimize polymer processing techniques (e.g., extrusion, injection molding, blow molding, etc.) to improve efficiency, reduce waste, and enhance material properties. R&D and Innovation : Collaborate in research and development efforts to innovate new polymer formulations, improve existing products, and explore new applications of polymer materials. Collaboration with Manufacturing : Work closely with manufacturing teams to ensure smooth transition from prototype to mass production, providing technical support and troubleshooting during scale-up processes. Quality Assurance : Implement quality control measures to ensure consistency and reliability of polymer materials and finished products. Documentation & Reporting : Prepare detailed technical reports, data sheets, and documentation for internal and external stakeholders. Regulatory Compliance : Stay current with industry regulations and ensure that polymer products meet required health, safety, and environmental standards. Qualifications: Education : Bachelor's or Master's degree in Polymer Engineering, Materials Science, Chemical Engineering, Industrial Engineering. Experience : At least 4-5 years of experience in polymer engineering or related industries. Experience in product development, material testing, and polymer processing is highly desirable. Technical Skills : Expertise in polymer chemistry and material properties, Extrusion Knowledge of polymer processing techniques (e.g., injection molding, extrusion, thermoforming). Familiarity with analytical techniques like spectroscopy, chromatography, and microscopy. Proficiency with engineering software (e.g., CAD, simulation tools). Soft Skills : Strong problem-solving and analytical skills. Excellent communication and collaboration abilities. Ability to work independently and as part of a team. Certifications : Relevant certifications in polymer technology or materials science are a plus. Preferred Skills: Experience with sustainable polymers, bio-based polymers, or biodegradable materials. Knowledge of ASTM, ISO, or other industry standards related to polymers. Previous experience in the medical, or packaging industries. Benefits: Competitive salary. Opportunities for professional development and career advancement. A dynamic and collaborative work environment. Job Type: Full-time Pay: ₹40,000.00 - ₹50,000.00 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Work Location: In person
You will be responsible for designing and developing medical device products with a focus on manufacturability. This includes evaluating customer designs and collaborating in a team setting to conduct research and development, initial design development, process/manufacturing R&D, and design. Your role will involve guiding and training technicians to successfully complete design and development projects. As part of your responsibilities, you will assess manufacturing processes by designing and implementing research programs, utilizing your knowledge of product design, fabrication, assembly, tooling, and materials. You will work closely with equipment vendors and operators to gather insights and improve manufacturing efficiency through analysis of work flow, space requirements, and equipment layout. Your contribution to the team effort will be crucial in achieving desired outcomes. You will actively participate in continuous improvement initiatives for all processes and provide support, cost estimates, and documentation for engineering changes. Additionally, you will take proactive measures to prevent nonconformance related to products, processes, and systems, and diligently document all activities as necessary. In this role, you may be assigned any additional responsibilities deemed essential by the Engineering Manager. This is a full-time position with benefits such as commuter assistance, health insurance, and provident fund. The work schedule is during the day shift, and there is a performance bonus incentive. The ideal candidate should hold a Bachelor's degree and have at least 1 year of relevant work experience. The work location is in person, and the successful candidate will be expected to contribute effectively to the design and development of medical device products while adhering to quality standards and continuous improvement practices.,
Job Description – Manufacturing Technician Position Title: Manufacturing Technician Department: Production / Manufacturing Reports To: Production Supervisor / Manufacturing Manager Job Summary The Manufacturing Technician is responsible for operating, monitoring, and maintaining manufacturing equipment and processes to ensure efficient production of high-quality products. The role involves troubleshooting machinery, performing quality checks, following safety standards, and supporting continuous improvement activities in the production area. Key Responsibilities Operate and monitor production machinery and equipment as per standard operating procedures (SOPs). Perform routine inspections, preventive maintenance, and minor repairs on equipment. Ensure compliance with safety, health, and environmental regulations at all times. Conduct quality checks to verify that products meet specifications and standards. Accurately record production data, including output, downtime, and process deviations. Assist in troubleshooting and resolving equipment or process issues to minimize downtime. Follow Good Manufacturing Practices (GMP) and maintain cleanliness of the production area. Collaborate with supervisors, engineers, and quality teams to improve efficiency and product quality. Support training of new operators or team members when required. Participate in continuous improvement initiatives such as lean manufacturing, 5S, and Kaizen. Qualifications & Skills Diploma / ITI / Bachelor’s degree in Mechanical, Electrical, Electronics, or related field. Proven experience in a manufacturing/production environment preferred. Knowledge of production processes, equipment operation, and safety practices. Ability to read technical drawings and follow SOPs. Strong problem-solving and troubleshooting skills. Good communication and teamwork abilities. Willingness to work in shifts and handle physically demanding tasks if required. Job Type: Permanent Pay: ₹11,000.00 - ₹12,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person
Job Overview: Embedded Systems Engineer (1–3 years) Company: Majik Medical Solutions Location: Hyderabad (On-site) Experience: 1–3 years Compensation: ₹3–4.5 LPA (CTC) Employment type: Full-time 1. About Majik Medical Solutions Majik builds next-gen medical devices, from health monitors to specialty generator systems—combining custom electronics, firmware, and cloud connectivity. You’ll join a hands-on team shipping real hardware that improves patient care. 2. Role summary You’ll design, build, and test embedded hardware and firmware: custom PCBs, low-power sensor nodes, device firmware (C/C++), and connectivity (BLE/Wi-Fi). You’ll own prototypes end-to-end schematic → layout → bring-up → validation—working closely with mechanical, QA/RA, and product teams. 3. What you’ll do - Electronics design: Capture schematics, size components, and lay out 2–6 layer PCBs (high-speed & mixed-signal basics, power domains, grounding, EMI/ESD practices).Firmware development: Write and debug C/C++ for MCUs (STM32/ESP32/nRF52 or similar), drivers for sensors/actuators, FreeRTOS tasks, power management, and simple bootloaders/OTA. - Connectivity/IoT: Implement BLE GATT, Wi-Fi + MQTT/HTTP, basic security (TLS, keys), and data protocols for device-to-app/cloud. - Bring-up & testing: Use oscilloscope, logic analyzer, DMM, power analyzer to verify boards; write test firmware; create validation reports. - Prototyping: Rework/soldering (0402/SOIC/QFN), lab builds, fixture wiring, and DFM/DFT notes for vendors (FAB/assembly). - Documentation: BOMs, revision notes, test plans, risk logs; maintain issue trackers (Git/Jira). - Quality & safety: Follow basic IEC 60601/EMC good practices in design; support verification records for ISO 13485 workflows (training provided). - Collaboration: Work with app/cloud teams on APIs and with mechanicals on enclosure/thermal/connector decisions. 4. Must-haves (1–3 years): - Hands-on PCB experience using KiCad or Altium (at least one board designed and tested end-to-end). - Solid C/C++ on microcontrollers; experience with STM32/ESP32 or similar; familiarity with Free RTOS. - Comfort with lab equipment (scope, LA) and debugging firmware/hardware interactions. - Basic analog skills: op-amp interfaces, sensor signal conditioning, ADC/DAC usage, filters, buck/linear regulators. - Exposure to BLE/Wi-Fi stacks and serial protocols (I²C, SPI, UART, CAN). - Clear documentation habits and version control (Git). Benefits: Competitive salary. Opportunities for professional development and career advancement. A dynamic and collaborative work environment. Job Type: Full-time Pay: ₹300,000.00 - ₹450,000.00 per year Benefits: Cell phone reimbursement Health insurance Provident Fund Work Location: In person
Job Title : Inventory Executive – Medical Devices Department : Supply Chain / Logistics Location : [Insert Location] Reports to : Inventory Manager / Supply Chain Manager Job Summary : The Inventory Executive is responsible for managing and maintaining accurate inventory records of medical devices and related supplies. This role ensures that stock levels are optimized, inventory is accurately tracked, and all regulatory and safety standards specific to medical devices are met. The Inventory Executive works closely with procurement, warehouse, and sales teams to ensure product availability and timely distribution. Key Responsibilities : Maintain accurate records of inventory levels, including incoming and outgoing stock. Conduct regular cycle counts and full physical inventory audits. Ensure compliance with healthcare regulations, including expiration tracking and storage requirements (e.g., cold chain, sterile conditions). Monitor stock levels and coordinate with procurement for timely reordering. Maintain inventory management systems (e.g., ERP software) and ensure real-time updates. Track serial numbers, batch numbers, and lot tracking for traceability and compliance. Handle damaged, expired, or returned goods as per standard operating procedures. Collaborate with warehouse and logistics teams to manage stock movement efficiently. Prepare inventory reports for internal audits, sales teams, and management. Support in demand forecasting by providing accurate inventory data and usage trends. Ensure safe handling, labeling, and storage of sensitive medical devices and instruments. Liaise with regulatory and QA teams during inspections or audits. Key Skills & Competencies : Strong knowledge of inventory management principles. Familiarity with regulatory requirements (e.g., FDA, CE, ISO 13485, GMP). Proficiency in inventory management systems (SAP, Oracle, Zoho Inventory, etc.). Strong attention to detail and organizational skills. Ability to work under pressure and manage multiple tasks. Effective communication and coordination skills. Basic understanding of medical device categories and handling requirements. Qualifications & Experience : Bachelor’s degree or related field. 2–4 years of experience in inventory or warehouse roles, preferably in the healthcare or medical devices industry. Experience with ERP systems and barcode/RFID inventory tracking is an advantage. Benefits: Competitive salary. Opportunities for professional development and career advancement. A dynamic and collaborative work environment. Job Type: Full-time Benefits: Cell phone reimbursement Health insurance Provident Fund Work Location: In person Job Type: Full-time Pay: ₹20,000.00 - ₹22,000.00 per month Work Location: In person
Role Overview: As an Embedded Systems Engineer with 13 years of experience at Majik Medical Solutions in Hyderabad, you will be responsible for designing, building, and testing embedded hardware and firmware for next-gen medical devices. You will work on custom PCBs, low-power sensor nodes, device firmware (C/C++), and connectivity (BLE/Wi-Fi), collaborating closely with mechanical, QA/RA, and product teams. Key Responsibilities: - Design electronics: Capture schematics, size components, and lay out 2-6 layer PCBs with a focus on high-speed & mixed-signal basics, power domains, grounding, and EMI/ESD practices. - Develop firmware: Write and debug C/C++ for MCUs such as STM32/ESP32/nRF52, create drivers for sensors/actuators, manage FreeRTOS tasks, implement power management, and develop simple bootloaders/OTA. - Implement connectivity/IoT: Set up BLE GATT, Wi-Fi + MQTT/HTTP, ensure basic security with TLS and keys, and establish data protocols for device-to-app/cloud communication. - Conduct bring-up & testing: Utilize oscilloscope, logic analyzer, DMM, and power analyzer for board verification, write test firmware, and compile validation reports. - Handle prototyping tasks: Perform rework/soldering (0402/SOIC/QFN), conduct lab builds, wire fixtures, and provide DFM/DFT notes for vendors (FAB/assembly). - Manage documentation: Create BOMs, revision notes, test plans, risk logs, and maintain issue trackers using Git/Jira. - Ensure quality & safety: Adhere to basic IEC 60601/EMC practices in design, support verification records for ISO 13485 workflows, and collaborate with app/cloud teams and mechanical teams on APIs and design decisions. - Collaborate with app/cloud teams on APIs and with mechanical teams on enclosure/thermal/connector decisions. Qualifications Required: - Hands-on PCB experience using KiCad or Altium with at least one board designed and tested end-to-end. - Proficiency in C/C++ programming on microcontrollers, experience with STM32/ESP32 or similar, and familiarity with FreeRTOS. - Comfort with lab equipment such as oscilloscope, logic analyzer, and debugging firmware/hardware interactions. - Basic analog skills including op-amp interfaces, sensor signal conditioning, ADC/DAC usage, filters, and buck/linear regulators. - Exposure to BLE/Wi-Fi stacks and serial protocols (IC, SPI, UART, CAN). - Strong documentation habits, version control using Git. Additional Company Details: Majik Medical Solutions is a company that specializes in building next-gen medical devices, from health monitors to specialty generator systems. They combine custom electronics, firmware, and cloud connectivity to create real hardware that improves patient care. Join their dynamic and collaborative work environment with opportunities for professional development and career advancement. Note: Cell phone reimbursement, health insurance, and Provident Fund benefits are provided. This is a full-time position based in Hyderabad.,
Job Summary: We are seeking a motivated and detail-oriented Regulatory Affairs Executive with 1–2 years of experience in the medical devices industry. The role involves supporting regulatory submissions, maintaining compliance with local and international regulations, and assisting in the preparation of technical documentation for product approvals and audits. This is a great opportunity for a candidate looking to grow their career in regulatory affairs within a dynamic and innovative medical device company. Key Responsibilities: Assist in the preparation and submission of regulatory documents for product registration and approvals (e.g., 510(k), CE Marking, CDSCO). Support the creation and maintenance of Technical Files, Design Dossiers, and product master files. Coordinate with internal teams (R&D, Quality, Manufacturing) to gather necessary documents for submissions. Monitor and interpret changes in global regulatory requirements and ensure compliance. Maintain databases and trackers for regulatory submissions, approvals, renewals, and other related activities. Assist with responding to queries from regulatory bodies and notified bodies. Help ensure that labeling, packaging, and promotional materials comply with applicable regulations. Support internal and external audits by providing relevant regulatory documents. Collaborate with senior team members to learn best practices and regulatory strategies. Requirements: Education: Bachelor’s degree in Life Sciences, Pharmacy, Biomedical Engineering, or a related field. Experience: 1–2 years of experience in Regulatory Affairs in the medical device or healthcare industry. Skills & Knowledge: Basic understanding of medical device regulations such as FDA 21 CFR Part 820, EU MDR 2017/745, or CDSCO. Familiarity with ISO 13485 and documentation standards. Good written and verbal communication skills. Attention to detail and strong organizational abilities. Ability to work collaboratively in a cross-functional team environment. Proficient in Microsoft Office (Word, Excel, PowerPoint). Preferred Qualifications (Optional): Internship or project experience related to regulatory affairs. Exposure to international regulatory submissions. Knowledge of risk management principles (e.g., ISO 14971). Career Development: This position offers excellent learning opportunities and career growth into roles such as Senior Regulatory Affairs Executive , Regulatory Specialist , or Regulatory Affairs Manager Job Type: Full-time Pay: ₹20,000.00 - ₹38,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person
Job Summary: We are seeking a motivated and detail-oriented Regulatory Affairs Executive with 1–2 years of experience in the medical devices industry. The role involves supporting regulatory submissions, maintaining compliance with local and international regulations, and assisting in the preparation of technical documentation for product approvals and audits. This is a great opportunity for a candidate looking to grow their career in regulatory affairs within a dynamic and innovative medical device company. Key Responsibilities: Assist in the preparation and submission of regulatory documents for product registration and approvals (e.g., 510(k), CE Marking, CDSCO). Support the creation and maintenance of Technical Files, Design Dossiers, and product master files. Coordinate with internal teams (R&D, Quality, Manufacturing) to gather necessary documents for submissions. Monitor and interpret changes in global regulatory requirements and ensure compliance. Maintain databases and trackers for regulatory submissions, approvals, renewals, and other related activities. Assist with responding to queries from regulatory bodies and notified bodies. Help ensure that labeling, packaging, and promotional materials comply with applicable regulations. Support internal and external audits by providing relevant regulatory documents. Collaborate with senior team members to learn best practices and regulatory strategies. Requirements: Education: Bachelor’s degree in Life Sciences, Pharmacy, Biomedical Engineering, or a related field. Experience: 1–2 years of experience in Regulatory Affairs in the medical device or healthcare industry. Skills & Knowledge: Basic understanding of medical device regulations such as FDA 21 CFR Part 820, EU MDR 2017/745, or CDSCO. Familiarity with ISO 13485 and documentation standards. Good written and verbal communication skills. Attention to detail and strong organizational abilities. Ability to work collaboratively in a cross-functional team environment. Proficient in Microsoft Office (Word, Excel, PowerPoint). Preferred Qualifications (Optional): Internship or project experience related to regulatory affairs. Exposure to international regulatory submissions. Knowledge of risk management principles (e.g., ISO 14971). Career Development: This position offers excellent learning opportunities and career growth into roles such as Senior Regulatory Affairs Executive , Regulatory Specialist , or Regulatory Affairs Manager Job Type: Full-time Pay: ₹20,000.00 - ₹38,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person
Company: GRK Medical ( MAJiK MEDICAL SOLUTIONS) Location: Tamil Nadu, Karnataka, and Andhra Pradesh (territory-based role) Experience: 3–5 years in Pharma / Medical Device Sales (clinical selling preferred) Education: Graduate in Science / Engineering / Pharmacy / Biotechnology / Healthcare (preferred) Employment Type: Full-time Salary: 42,000-80,000 About GRK Medical At GRK Medical, we are committed to transforming patient care by delivering advanced cardiac and neuro solutions that truly impact lives. Our strength lies in clinical credibility, strong partnerships with healthcare professionals, and a relentless pursuit of excellence. We are looking for ambitious professionals who want more than just “a sales job.” If you believe in making a clinical difference, building value-driven relationships, and growing with a high-performance culture, then this is the right place for you. The Challenge This is not a typical sales role. As an Area Manager, you will wear two hats: 1. Clinical Support Specialist – providing in-depth product knowledge, clinical demonstrations, and training to doctors, nurses, and technicians. 2. Sales Leader – driving adoption, managing distributors, and delivering business growth in a competitive market. Your ability to combine clinical communication with commercial acumen will set you apart. Key Responsibilities Drive Clinical Sales: Position GRK’s cardiac and neuro devices as preferred solutions through meaningful, clinically relevant conversations with doctors and HCPs. Influence Decision-Makers: Build strong networks with clinicians, purchase managers, technicians, and distributors, creating trust and credibility that drives adoption. Distributor & Channel Excellence: Appoint, train, and manage distributors; ensure seamless supply and execution of urgent deliveries when required. Clinical Support & Training: Conduct hands-on product demos, operating room support (where relevant), CME participation, and ongoing training for healthcare professionals. Market Intelligence: Track competitor activities, market gaps, and emerging opportunities—translate insights into strategies. Ownership & Accountability: Manage sales targets with complete responsibility for your territory—results will speak louder than effort. What We Expect from You Proven experience (3–5 years) in pharma or medical device sales, ideally in cardiology, neurology, or other specialty-driven therapies. Strong clinical communication skills—you must be comfortable talking medical language with doctors and explaining device utility with authority. Entrepreneurial mindset—this role rewards those who take ownership, not those who wait for instructions. High energy and resilience—daily travel, demanding targets, and hospital-level engagements are part of the game. Ethical and professional integrity—your credibility in the clinical community will be your greatest asset. What We Offer Competitive salary aligned with industry benchmarks. Attractive performance-linked incentives—high achievers will see significant financial rewards. Fast-track career growth—clear pathways for promotion into leadership roles for those who excel in clinical communication and business impact. Comprehensive training—both product and clinical communication training to sharpen your edge. Exposure to advanced therapies in a high-growth sector that shapes the future of healthcare. This is a role for candidates who want to make an impact—both clinically and commercially. If you’re simply looking for an easy sales job, this isn’t for you. If you want to push yourself, build deep clinical credibility, and grow with strong rewards, GRK Medical is where you belong. Job Type: Full-time Pay: ₹42,000.00 - ₹80,000.00 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Work Location: In person