We are seeking a skilled PCB Soldering Technician to join our production and assembly team. The candidate will be responsible for assembling, soldering, reworking, and inspecting printed circuit boards (PCBs) according to engineering specifications, IPC standards, and quality requirements. This role requires attention to detail, steady hand coordination, and knowledge of both through-hole and surface mount soldering techniques. Key Responsibilities Perform manual soldering of electronic components (through-hole and SMD) on PCBs. Operate soldering tools, hot air stations, and reflow equipment as required. Read and interpret circuit diagrams, assembly drawings, and work instructions . Perform rework and repair of PCBs including component replacement, jumper wiring, and fault correction. Inspect solder joints and assemblies using microscopes, magnifiers, and AOI standards . Follow IPC-A-610 and other industry standards for soldering and assembly quality. Handle ESD-sensitive components safely following ESD protocols. Maintain soldering equipment, tools, and ensure the workplace is clean and safe. Document assembly processes, test results, and report any defects or issues. Collaborate with engineers and production supervisors to resolve assembly challenges. Qualifications High school diploma, ITI, Diploma in Electronics, or equivalent technical training. Proven experience in manual soldering and PCB assembly . Knowledge of electronic components and symbols. Certification in IPC-A-610 / J-STD-001 (preferred). Ability to use soldering irons, hot air guns, reflow ovens, microscopes, and hand tools. Strong attention to detail, patience, and manual dexterity. Ability to work independently and as part of a production team. Skills Required Through-hole and SMD soldering (hand and rework). Familiarity with ESD practices and safe component handling. Ability to identify components, polarity, and orientation. Good hand-eye coordination and fine motor skills. Basic troubleshooting of soldering and assembly defects. Work Environment Production floor / electronics assembly line. May require sitting or standing for long periods. Use of microscopes, soldering irons, rework stations, and testing tools. Must adhere to safety, quality, and ESD protocols. Job Types: Full-time, Contractual / Temporary Contract length: 6 months Pay: ₹15,453.52 - ₹25,288.17 per month Work Location: In person
Position Summary: We are seeking a detail-oriented and proactive Accounts Admin Executive to manage financial records, tender documentation, and administrative processes. The role requires maintaining accurate accounts, ensuring compliance with statutory requirements, and supporting day-to-day business operations. Key Responsibilities Tender Management View, download, and submit tender documents on behalf of the company. Maintain a proper record of all tender submissions and related documentation. Accounting & Bookkeeping Update and maintain all financial entries in Zoho Books/Zoho Finance Suite . Prepare and maintain balance sheets, P&L statements, and other financial reports . Assist in statutory filings and ensure compliance with company accounting standards. Logistics & Compliance Generate and manage e-Way bills for goods movement as per GST guidelines. Ensure timely submission and compliance with government regulations. Procurement & Purchase Create, issue, and track Purchase Orders (POs) . Receive, verify, and record supplier Purchase Orders. Maintain vendor records and coordinate with suppliers for smooth transactions. Documentation & Administration Ensure all company documents, licenses, and certificates are updated and organized. Maintain records for audits, compliance checks, and internal reviews. Support management in day-to-day administrative and operational tasks. Qualifications & Skills Bachelor’s degree in Commerce, Accounting, Finance, or Business Administration . 2–4 years of relevant experience in accounts and administration. Hands-on experience with Zoho Books / Tally / ERP software . Knowledge of GST, e-Way bills, and statutory compliance . Strong proficiency in MS Excel, Word, and documentation . Excellent organizational and multitasking abilities. Strong attention to detail with the ability to meet deadlines. Preferred Attributes Experience in handling tenders and government portal submissions . Ability to work independently and manage confidential information. Good communication and coordination skills with internal teams and vendors. Job Type: Full-time Pay: ₹20,240.06 - ₹30,591.47 per month Work Location: In person
Position Summary: We are seeking a detail-oriented and proactive Accounts Admin Executive to manage financial records, tender documentation, and administrative processes. The role requires maintaining accurate accounts, ensuring compliance with statutory requirements, and supporting day-to-day business operations. Key Responsibilities Tender Management View, download, and submit tender documents on behalf of the company. Maintain a proper record of all tender submissions and related documentation. Accounting & Bookkeeping Update and maintain all financial entries in Zoho Books/Zoho Finance Suite . Prepare and maintain balance sheets, P&L statements, and other financial reports . Assist in statutory filings and ensure compliance with company accounting standards. Logistics & Compliance Generate and manage e-Way bills for goods movement as per GST guidelines. Ensure timely submission and compliance with government regulations. Procurement & Purchase Create, issue, and track Purchase Orders (POs) . Receive, verify, and record supplier Purchase Orders. Maintain vendor records and coordinate with suppliers for smooth transactions. Documentation & Administration Ensure all company documents, licenses, and certificates are updated and organized. Maintain records for audits, compliance checks, and internal reviews. Support management in day-to-day administrative and operational tasks. Qualifications & Skills Bachelor’s degree in Commerce, Accounting, Finance, or Business Administration . 2–4 years of relevant experience in accounts and administration. Hands-on experience with Zoho Books / Tally / ERP software . Knowledge of GST, e-Way bills, and statutory compliance . Strong proficiency in MS Excel, Word, and documentation . Excellent organizational and multitasking abilities. Strong attention to detail with the ability to meet deadlines. Preferred Attributes Experience in handling tenders and government portal submissions . Ability to work independently and manage confidential information. Good communication and coordination skills with internal teams and vendors. Job Type: Full-time Pay: ₹20,240.06 - ₹30,591.47 per month Work Location: In person
About the Role: We are seeking a highly skilled and innovative Product Design Engineer to join our dynamic team. The successful candidate will play a pivotal role in designing and developing products from concept to production, utilizing software such as AutoCAD, Inventor, and SolidWorks. This role requires close collaboration with production vendors to ensure designs are manufacturable and meet all necessary specifications. Key Responsibilities: Product Design and Development: Design and develop new products from concept through to production. Create detailed 3D models and 2D drawings using AutoCAD, Inventor, and SolidWorks. Perform simulations and analysis to verify the integrity and functionality of designs. Vendor Collaboration: Work closely with production vendors to ensure designs are feasible and cost-effective. Modify designs based on feedback from production vendors to optimize manufacturability. Conduct design reviews and provide technical support to vendors during the manufacturing process. Project Management: Manage multiple projects simultaneously, ensuring timely delivery of design milestones. Prepare and maintain design documentation, including specifications, design reviews, and testing reports. Communicate effectively with cross-functional teams to ensure alignment and project success. Quality and Compliance: Ensure all designs meet industry standards and regulatory requirements. Conduct design verification and validation to ensure product quality and reliability. Implement design changes and improvements based on testing results and customer feedback. Continuous Improvement: Stay updated with the latest design software and industry trends. Suggest and implement improvements to design processes and workflows. Participate in continuous improvement initiatives to enhance product design and development efficiency. Qualifications: Education: Bachelor’s degree in Mechanical Engineering, Industrial Design, or a related field. Experience: Minimum of 3-5 years of experience in product design and development. Proven experience with AutoCAD, Inventor, and SolidWorks. Experience working with production vendors and understanding of manufacturing processes. Skills: Strong knowledge of design principles, materials, and manufacturing processes. Excellent problem-solving skills and attention to detail. Ability to manage multiple projects and meet deadlines. Strong communication and interpersonal skills. Ability to work collaboratively in a team environment. Benefits: Competitive salary and performance-based bonuses. Health, dental, and vision insurance. Retirement savings plan with company match. Opportunities for professional development and career advancement. Flexible work hours and a supportive work environment. Job Type: Full-time Pay: ₹376,318.05 - ₹525,455.14 per year Experience: total work: 2 years (Preferred) Work Location: In person
Role Overview We are hiring a meticulous ISO / GMP / CE Documentation Specialist to build, maintain, and control all compliance documentation required across our product portfolio. This role ensures that every document—SOPs, technical files, risk assessments, process records, regulatory submissions, and audit-ready materials—is accurate, current, and aligned with international quality standards. This is a documentation-heavy role requiring exceptional attention to detail, strong process understanding, and the ability to collaborate closely with engineering, production, R&D, and regulatory teams. Key Responsibilities 1. ISO Documentation Management Create, organize, and maintain documentation for: ISO 9001 QMS ISO 13485 (medical device processes), where applicable Own and manage: SOPs Work Instructions Quality Manuals Process flowcharts NCR/CAPA records Internal audit documentation Ensure document traceability, version control, and adherence to QMS requirements. 2. GMP Documentation Maintain GMP-required records including: Batch manufacturing records Device history records (DHR) Device master records (DMR) Calibration + maintenance logs Training records and competency matrices Ensure all logs and templates follow traceability, compliance, and regulatory formatting norms. 3. CE Documentation (Technical Files) Prepare and maintain CE Technical Documentation for each product: Essential Requirements/General Safety & Performance Checklist Risk Management File (ISO 14971-based) EMC/EMI/ESD test reports Labeling artwork, IFUs, packaging validation BOM traceability and component declarations (RoHS, REACH, etc.) DoC (Declaration of Conformity) Organize test evidence, third-party lab reports, and certifications for audit readiness. 4. Document Control & Compliance Tracking Own the complete document control system—creation, review, approval, release, archival. Manage controlled distribution of documents to production, engineering, R&D, and QC teams. Ensure expired/obsolete documents are removed or updated. Monitor compliance timelines, renewal dates, and corrective actions needing documentation updates. 5. Audit Support Prepare audit binders, evidence logs, and process documentation for: Internal audits ISO surveillance audits CE technical documentation reviews GMP inspections Ensure all required documents are audit-ready at all times. 6. Cross-Functional Coordination Work closely with engineering to capture design documentation. Work with manufacturing to document processes, QC steps, calibration procedures, and production records. Collaborate with regulatory teams for submissions, declarations, and compliance updates. Train internal teams on documentation discipline and QMS procedures. Required Qualifications Bachelor’s degree (Engineering, Life Sciences, Quality Management, or related field). 1–4 years of experience specifically in ISO / GMP / CE documentation . Strong understanding of QMS frameworks and regulatory requirements. Excellent writing, document formatting, and technical editing skills. Familiarity with risk management, QC processes, and audit preparation. Preferred Skills Experience working in electronics, medical devices, diagnostics, or instrumentation industries. Understanding of standards such as ISO 14971, IEC 60601, IEC 61010, RoHS, REACH, etc. Ability to interpret engineering drawings, test reports, and BOMs. Proficiency with document control software or QMS tools. Strong organizational and archival discipline. What We Offer A role that directly strengthens our compliance backbone across multiple advanced instrumentation products. Exposure to real-world international certification workflows (ISO, CE, GMP). Clear growth path into Regulatory Affairs, Quality Systems, or Compliance Engineering roles. Competitive salary and performance-based growth opportunities. Job Type: Full-time Pay: ₹13,763.05 - ₹31,244.75 per month Benefits: Provident Fund Work Location: In person
Role Overview We are looking for a highly disciplined Process Quality Engineer to own and maintain all quality, regulatory, and compliance frameworks across the company. This role is central to ensuring that every product—hardware, embedded systems, software, and instrumentation—meets ISO, GMP, CE, and other relevant international standards. You will be the custodian of quality documentation, process integrity, audits, risk analysis, and corrective actions across the entire product lifecycle: design, manufacturing, testing, calibration, and field deployment. Key Responsibilities 1. Standards & Compliance Management Maintain, update, and enforce compliance with: ISO 9001 (Quality Management Systems) ISO 13485 (Medical Device Quality Systems), where applicable GMP requirements for medical/diagnostic instrumentation CE documentation (technical files, risk assessment, EMC/Safety test data) for all products Any additional regulatory frameworks (AERB, BIS, IEC, RoHS, FCC where applicable) 2. Documentation Control Own and maintain all Quality System Documents (QSD) including SOPs, Work Instructions, Process Flow Charts, QMS forms, NCR logs, calibration logs, device history records (DHR), device master records (DMR), etc. Create, update, and control documentation for each product line (HFCM, XSpec, DetecX, SiPM modules, FPGA boards, dosimeters, etc.). Ensure revision control, document traceability, and version management. 3. Manufacturing Process Quality Establish and maintain incoming, in-process, and final QC procedures. Validate and optimize processes for PCB assembly, calibration workflows, high-voltage testing, sensor verification, and environmental testing. Implement sampling plans, inspection criteria, and statistical quality control (SPC). Audit suppliers for component and assembly quality. 4. Product Certification Support Prepare and maintain CE Technical Documentation for each product: Essential Requirements Checklist Risk Assessment (ISO 14971) EMC and Electrical Safety test documentation BOM traceability, labeling conformity, DoC (Declaration of Conformity) Coordinate with external labs for EMC, EMI, ESD, environmental, and safety testing. 5. Quality Audits Plan and execute internal quality audits. Coordinate external audits and surveillance visits (ISO auditors, notified bodies, regulatory agencies). Drive CAPA (Corrective and Preventive Actions) to closure with engineering and production teams. Ensure audit findings are documented, tracked, and verified. 6. Risk Management & Failure Analysis Perform FMEA for processes and products. Lead investigations for field failures, RMAs, device malfunctions, and non-conformities. Work closely with engineering and manufacturing to implement corrective actions. 7. Training & Process Enforcement Train staff on SOPs, QC procedures, documentation discipline, and regulatory requirements. Ensure cross-department adherence to quality processes. Promote a culture of continuous improvement. Required Qualifications Bachelor’s degree in Mechanical, Electronics, Industrial Engineering, or related field. 2–5 years experience in Quality Engineering (medical devices, electronics, instrumentation, or similar industries preferred). Strong understanding of ISO/GMP/CE and regulatory compliance documentation. Experience with risk assessment tools (FMEA, Fault Tree Analysis, etc.). Familiarity with calibration procedures, QC instrumentation, and production workflows. Excellent documentation, organizational, and reporting skills. Preferred Skills Experience with EMC/EMI testing and CE certification processes. Knowledge of AERB/BIS/IEC safety standards (for nuclear/medical instrumentation). Understanding of PCB manufacturing, embedded systems, FPGA/controller hardware, and sensor devices. Working knowledge of statistical tools (SPC, Minitab, JMP, etc.). Ability to read schematics, BOMs, and mechanical drawings. What We Offer Opportunity to shape the quality backbone of an advanced instrumentation company. Work across multiple innovative product lines in nuclear medicine, radiation safety, and precision electronics. Fast-paced environment with autonomy, responsibility, and growth potential. Competitive salary and performance-based incentives. Job Type: Full-time Pay: ₹216,019.76 - ₹468,260.35 per year Benefits: Provident Fund Work Location: In person
Role Overview We are hiring a meticulous ISO / GMP / CE Documentation Specialist to build, maintain, and control all compliance documentation required across our product portfolio. This role ensures that every document—SOPs, technical files, risk assessments, process records, regulatory submissions, and audit-ready materials—is accurate, current, and aligned with international quality standards. This is a documentation-heavy role requiring exceptional attention to detail, strong process understanding, and the ability to collaborate closely with engineering, production, R&D, and regulatory teams. Key Responsibilities 1. ISO Documentation Management Create, organize, and maintain documentation for: ISO 9001 QMS ISO 13485 (medical device processes), where applicable Own and manage: SOPs Work Instructions Quality Manuals Process flowcharts NCR/CAPA records Internal audit documentation Ensure document traceability, version control, and adherence to QMS requirements. 2. GMP Documentation Maintain GMP-required records including: Batch manufacturing records Device history records (DHR) Device master records (DMR) Calibration + maintenance logs Training records and competency matrices Ensure all logs and templates follow traceability, compliance, and regulatory formatting norms. 3. CE Documentation (Technical Files) Prepare and maintain CE Technical Documentation for each product: Essential Requirements/General Safety & Performance Checklist Risk Management File (ISO 14971-based) EMC/EMI/ESD test reports Labeling artwork, IFUs, packaging validation BOM traceability and component declarations (RoHS, REACH, etc.) DoC (Declaration of Conformity) Organize test evidence, third-party lab reports, and certifications for audit readiness. 4. Document Control & Compliance Tracking Own the complete document control system—creation, review, approval, release, archival. Manage controlled distribution of documents to production, engineering, R&D, and QC teams. Ensure expired/obsolete documents are removed or updated. Monitor compliance timelines, renewal dates, and corrective actions needing documentation updates. 5. Audit Support Prepare audit binders, evidence logs, and process documentation for: Internal audits ISO surveillance audits CE technical documentation reviews GMP inspections Ensure all required documents are audit-ready at all times. 6. Cross-Functional Coordination Work closely with engineering to capture design documentation. Work with manufacturing to document processes, QC steps, calibration procedures, and production records. Collaborate with regulatory teams for submissions, declarations, and compliance updates. Train internal teams on documentation discipline and QMS procedures. Required Qualifications Bachelor’s degree (Engineering, Life Sciences, Quality Management, or related field). 1–4 years of experience specifically in ISO / GMP / CE documentation . Strong understanding of QMS frameworks and regulatory requirements. Excellent writing, document formatting, and technical editing skills. Familiarity with risk management, QC processes, and audit preparation. Preferred Skills Experience working in electronics, medical devices, diagnostics, or instrumentation industries. Understanding of standards such as ISO 14971, IEC 60601, IEC 61010, RoHS, REACH, etc. Ability to interpret engineering drawings, test reports, and BOMs. Proficiency with document control software or QMS tools. Strong organizational and archival discipline. What We Offer A role that directly strengthens our compliance backbone across multiple advanced instrumentation products. Exposure to real-world international certification workflows (ISO, CE, GMP). Clear growth path into Regulatory Affairs, Quality Systems, or Compliance Engineering roles. Competitive salary and performance-based growth opportunities. Job Type: Full-time Pay: ₹13,763.05 - ₹31,244.75 per month Benefits: Provident Fund Work Location: In person
About the Role We are looking for a technically strong Scientific Simulation Intern to design, implement, and run physics-based simulations using GEANT4. The role focuses on modeling physical interactions, materials, and geometries, running computational experiments, and analyzing results. This internship is hands-on and code-heavy. You will be expected to build simulations from scratch, validate results, and iterate based on experimental or theoretical inputs. What You Will Work On Developing GEANT4 simulations for physical interaction modeling Creating and validating 3D geometries and material definitions Running Monte Carlo simulations and analyzing outputs Optimizing simulation parameters for accuracy and performance Comparing simulation results with measured or reference data Documenting models, assumptions, and results clearly Required Skills Strong fundamentals in physics, applied mathematics, or engineering Working knowledge of C++ Familiarity with Linux / macOS command-line environments Basic understanding of numerical methods or Monte Carlo simulations Ability to read technical papers and implement models from literature Preferred (Not Mandatory) Prior exposure to GEANT4, MCNP, FLUKA, or similar simulation frameworks Experience with data analysis tools (Python, ROOT, MATLAB, etc.) Basic understanding of materials, detectors, or sensor modeling Experience compiling large C++ projects (CMake, Make, Ninja) Who Should Apply Final-year undergraduate students, master's students, or early PhD candidates Students comfortable with coding + physics, not just theory Self-driven learners who can debug, iterate, and validate their own work Candidates interested in computational modeling and scientific software development What You Will Gain Real-world experience building production-grade scientific simulations Deep exposure to Monte Carlo methods and physics-based modeling Mentorship in simulation design, validation, and result interpretation Opportunity to contribute to publishable or product-grade simulation work Strong portfolio project for higher studies or R&D roles Selection Process Short technical screening (physics + coding) Small take-home or live simulation exercise Technical discussion on modeling approach and assumptions Job Type: Internship Contract length: 3 months Pay: ₹13,000.00 - ₹25,000.00 per month Work Location: In person