BigTec Careers

Join us in Reshaping the Future of Healthcare

We are dedicated to cultivating a workplace that embraces diversity in every aspect – from backgrounds and experiences to perspectives. We believe that inclusivity drives our innovation.

We actively seek talented individuals with unique viewpoints and ideas. By welcoming these differences, we foster a dynamic environment where creativity thrives and ground-breaking solutions emerge.

Current job openings

Manager Embedded Electronics (COE)

Job Description

 

    • Lead product design and development from concept to validation and transfer to manufacturing, ensuring technical and process integrity.

    • Provide technical leadership in developing embedded hardware and firmware architectures for medical diagnostic devices, ensuring seamless integration with sensors, actuators, optics, and mechanical subsystems.
    • Oversee development of embedded hardware and firmware designs to ensure robustness, power efficiency, and compliance with medical safety standards.

    • Guide component selection, including microcontrollers, ADCs, DACs, and communication interfaces, to balance performance, reliability, and cost.

    • Embed DFX principles throughout design and development to enhance manufacturability, assembly, serviceability, and scalability.

    • Drive execution and review of embedded design and verification processes, including schematic validation, PCB bring-up, and firmware testing, to confirm functionality and mitigate early-stage risks.

    • Lead root-cause analysis and resolution of embedded hardware and firmware issues, ensuring timely corrective and preventive actions.

    • Plan and spearhead prototype and pilot builds across projects, ensuring hardware validation, firmware readiness, and manufacturing scalability.

    • Drive hardware and firmware reliability, EMC/EMI, and environmental testing to establish verification data for product qualification.

    • Collaborate with suppliers, OEMs, and manufacturing partners to enable reliable, scalable, and timely production of electronic assemblies.

    • Manage effective use of development tools, lab equipment, and testing infrastructure to enable domain-level prototyping and verification.

Key Requirements

  • Bachelor’s or Master’s degree in Electronics, Electrical, or Embedded Systems Engineering, with at least 12 years of experience in embedded hardware and firmware design for medical or safety-critical devices.

  • Hands-on expertise in embedded systems architecture, microcontrollers, RTOS, and communication protocols (UART, SPI, I²C, CAN, BLE, Wi-Fi).

  • Experience in PCB design, hardware bring-up, and debugging using oscilloscopes, logic analyzers, and automated test systems.

  • Strong understanding of design controls, verification and validation (V&V), and regulatory documentation

  • Knowledge of applicable standards including ISO 13485, ISO 14971, ISO 10993 and IEC 60601.

Other Information

 

Manager Analog Electronics ( COE )

Job Description

 

      • Lead product design and development from concept to validation and transfer to manufacturing, ensuring technical and process integrity.
      • Provide technical leadership in developing analog and mixed-signal circuits for medical diagnostic devices, ensuring seamless integration with embedded, optical, and mechanical subsystems.

      • Oversee design and optimization of precision analog front ends, amplifiers, filters, and power supplies to achieve low noise, high stability, and long-term reliability.

      • Guide component selection, including ADCs, DACs, op-amps, and precision timing devices, balancing performance, reliability, and cost.

      • Embed DFX principles throughout design and development to enhance manufacturability, assembly, serviceability, and scalability.

      • Plan and spearhead prototype and pilot builds across projects, ensuring analog module validation, test readiness, and manufacturing scalability.

      • Drive reliability, EMC/EMI, and environmental testing to establish verification data for product qualification.

      • Collaborate with suppliers, OEMs, and manufacturing partners to ensure reliability, scalability, and production readiness of analog subsystems.

      • Define and implement manufacturing enablers such as test jigs, calibration setups, and inspection systems to ensure consistency, quality, and cost efficiency.

      • Ensure adherence to ISO 13485, IEC 60601, and related standards governing electronic and safety-critical designs.

      • Oversee creation and maintenance of technical and regulatory documentation, including DHF, DMR, test reports, and risk files, ensuring audit readiness and compliance.

      • Manage effective use of lab facilities, instruments, and prototyping resources to enable domain-level testing and continuous improvement.

      • Mentor engineers, foster collaboration, and manage timelines, risks, and deliverables to ensure project success.

Key Requirements

        • Bachelor’s or Master’s degree in Electronics, Electrical, or Instrumentation Engineering, with at least 12 years of experience in analog and mixed-signal design for medical or safety-critical applications.
        • Proven expertise in precision analog circuit design, low-noise sensor interfaces, and mixed-signal integration (ADCs, DACs, timing circuits).

        • Experience with EMI/EMC mitigation, power supply design, and signal conditioning for high-accuracy diagnostic systems.

        • Proficiency in circuit simulation and modeling tools (SPICE, LTspice, PSpice) and validation of analog performance through testing and fixture design.

        • Strong understanding of design controls, verification and validation (V&V), and regulatory documentation (DHF, DMR, risk management files).

Other Information

 

Manager Mechanical Engineering ( COE )

Job Description

 

      • Lead product design and development from concept to validation and transfer to manufacturing, ensuring technical and process integrity.

      • Provide technical leadership in developing mechanical subsystems that integrate seamlessly with optics, microfluidics, electronics, and software to deliver robust, compact diagnostic devices.
      • Oversee the design of enclosures, mechanisms, thermal management solutions, and structural components optimized for medical device use.

      • Guide material and process selection to ensure biocompatibility, durability, and cost- effectiveness.

      • Ensure DFX principles are embedded throughout design and development to enhance manufacturability, assembly, serviceability, and scalability.

      • Ensure mechanical simulations, including structural, dynamic, and tolerance analyses, are effectively planned, executed, and reviewed to verify integrity and mitigate early-stage risks.

      • Lead investigation and resolution of mechanical and system-interface failures, ensuring timely root-cause analysis and corrective actions.

      • Collaborate with suppliers, OEMs, and manufacturing partners to enable reliable, scalable, and timely production.

      • Define and implement manufacturing enablers such as fixtures, automation, and inspection systems to ensure consistency, quality, and cost efficiency.

      • Establish and maintain mechanical design standards, best practices, and reusable design frameworks.

      • Lead design reviews, risk analyses, and verification plans with cross-functional teams.

      • Ensure adherence to ISO 13485, ISO 14971, and related standards during design and verification.

      • Supervise creation and maintenance of technical and regulatory documentation, including DHF, DMR, and risk files, ensuring audit readiness and compliance.

Key Requirements

      • Bachelor’s or Master’s degree in Mechanical Engineering or a related field, with at least 12 years of experience in product design and development for medical or other safety-critical devices.
      • Proven expertise in mechanical design of enclosures, mechanisms, and structural components, with proficiency in CAD modeling, tolerance analysis, and DFM/DFA principles.

      • Experience in materials selection, mechanical simulations, and reliability testing (vibration, drop, thermal) to ensure manufacturability and durability.

Other Information

 

Analyst - Mass Spectrometry

Job Description

    • Lead product design and development from concept to validation and transfer to manufacturing, ensuring technical and process integrity.

    • Provide technical leadership in developing analog and mixed-signal circuits for medical diagnostic devices, ensuring seamless integration with embedded, optical, and mechanical subsystems.
    • Oversee design and optimization of precision analog front ends, amplifiers, filters, and power supplies to achieve low noise, high stability, and long-term reliability.

    • Guide component selection, including ADCs, DACs, op-amps, and precision timing devices, balancing performance, reliability, and cost.

    • Embed DFX principles throughout design and development to enhance manufacturability, assembly, serviceability, and scalability.

    • Plan and spearhead prototype and pilot builds across projects, ensuring analog module validation, test readiness, and manufacturing scalability.

    • Drive reliability, EMC/EMI, and environmental testing to establish verification data for product qualification.

    • Collaborate with suppliers, OEMs, and manufacturing partners to ensure reliability, scalability, and production readiness of analog subsystems.

    • Define and implement manufacturing enablers such as test jigs, calibration setups, and inspection systems to ensure consistency, quality, and cost efficiency.

    • Ensure adherence to ISO 13485, IEC 60601, and related standards governing electronic and safety-critical designs.

    • Oversee creation and maintenance of technical and regulatory documentation, including DHF, DMR, test reports, and risk files, ensuring audit readiness and compliance.

    • Manage effective use of lab facilities, instruments, and prototyping resources to enable domain-level testing and continuous improvement.

    • Mentor engineers, foster collaboration, and manage timelines, risks, and deliverables to ensure project success.

Key Requirements

  • Post graduate/PhD in:  Analytical chemistry (with specialization in Mass Spec) or Physics.

Other Information

 

Manager/Associate Manager (Strategy ,Business Development and Operations)

Job Description

  • We are seeking a highly motivated and results-oriented Manager, Strategy, Business Development &
    Operations to join our dynamic strategy team. In this critical role, you will play a pivotal role in
    shaping the company’s future by developing and implementing a comprehensive biomedical
    technology strategy that fosters innovation and drives growth.

Key Requirements

  • Understand company’s needs and Strategy for cutting-edge biomedical technologies.
  •  Proactively identify and rigorously evaluate biomedical technologies with high
    potential for improving patient care, Go-to-Market strategies and impact.
  •  Prepare reports and documents on various biomedical technologies
  • Develop and manage strategic programs, including technology acceleration
    initiatives, to facilitate the rapid deployment and assessment of promising
    technologies.
  •  Craft cohesive strategies to enhance organizational efficiency and streamline
    operations.
  • Oversee internal and external projects, proactively identifying and mitigating risks,
    and resolving bottlenecks to ensure timely and successful project completion.
  •  Prepare periodic project management reports
  • Build and maintain strong relationships with internal and external stakeholders,
    fostering effective collaboration across all levels.
  • Champion the company’s  brand through strategic communication initiatives across
    online and offline channels, including social media platforms like LinkedIn.
  • Proactively engage with companies, global organizations, and academia to cultivate
    strategic partnerships and expand the company’s reach.
  • Represent the company at various fora

Qualifications

    •  Bachelor’s degree (B.Tech./B.Sc./BS) in Science (preferably Biomedical Science), Engineering,
      Life Sciences, or a related fields.

    • Minimum 3 years of experience in the healthcare sector, with a preference for medtech
      experience.

    • Proven proficiency in MS Office Suite and project management tools (e.g., Gantt charts).

    • Excellent written and verbal communication skills with the ability to tailor communication to
      diverse audiences.

    •  Strong analytical and problem-solving abilities with a strategic mindset.

    • Familiarity with social media communication platforms and best practices (desirable).

    •  A passion for innovation and a strong understanding of the biomedical technology landscape
      and product development process.

    • ————— Other Information ————————-
    • Role:   Manager/Associate Manager (Startegy,Business Development and Operations)

    • Job Location: Bangalore
    • Contact Mail Id: career@bigtec.co.in , hr@bigtec.co.in