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Mechanical design engineer

  • Vadodara, Gujarat
  • On-Site
We would love to share a similar experience and how I learned some valuable lessons.

PCB Design Engineer

  • Vadodara, Gujarat
  • On-Site
We would love to share a similar experience and how I learned some valuable lessons.

Firmware Engineer

  • Vadodara, Gujarat
  • On-Site
We would love to share a similar experience and how I learned some valuable lessons.

QA/RA Engineer

  • Vadodara, Gujarat
  • On-Site
We would love to share a similar experience and how I learned some valuable lessons.

Job Description

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    Mechanical Design Engineer

    Experience

    3 to 6 Years

    About SILMATES

    Silmates Pvt. Ltd. is a service provider in the medical equipment domain, working with offshore clients on:

    • New Product Development (NPD)
    • Sustenance Engineering
    • Testing & Verification/Validation (V&V)
    • End-to-end product development (Concept to Market)
    Job Description
    • Design, develop, and improve electro-mechanical modules and existing products for better quality, reliability, and cost-effectiveness.
    • Work with cross-functional teams to meet customer requirements.
    • Use CAD/CAE tools (SolidWorks or similar) to create 2D/3D designs and documentation.
    • Follow the Engineering Change Order (ECO) process.
    • Support continuous improvement in design, manufacturing, and product quality.
    • Ensure designs meet performance, quality, cost, and documentation standards.
    • Integrate components into modular designs as per specifications.
    • Mentor junior engineers and support team development.
    Responsibilities
    • Manage and maintain product data in company systems.
    • Lead and participate in client project meetings.
    • Support assembly and testing of components, troubleshooting issues if needed.
    • Prepare clear technical documentation.
    Qualifications
    • B.E./B.Tech in Mechanical Engineering (or equivalent).
    • Knowledge of ECO process & documentation.
    • SolidWorks certification (preferred).
    Competencies
    • SolidWorks PDM
    • Strong communication skills

    PCB Design Engineer

    Experience

    2 to 4 Years

    About SILMATES

    Silmates Pvt. Ltd. provides services in the medical equipment domain, working with offshore clients on:

    • New Product Development (NPD)
    • Sustenance Engineering
    • Testing & V&V
    • End-to-end product development (Concept to Market)
    Technical Skills
    • Strong knowledge of datasheets, library creation, and IPC standards for PCB design.
    • Expertise in high-speed, multilayer PCB design (analog, digital, power circuits).
    • Hands-on experience with signal routing, constraint setting, and DFM checks.
    • Familiar with interfaces and protocols: I2C, SPI, USB 2.0/3.0, Ethernet, PoE, BLE, Wi-Fi, GSM, TFT LCD, DDR2/3/4, SD Card, NAND, MIPI, Optical.
    • Proficient in DRC, Gerber release, fabrication & assembly file generation.
    • Skilled in PCB design best practices including RF, EMI/EMC, surge, and impedance control.
    • Collaboration with Design, Mechanical, SI/PI, Thermal, FAB & Assembly teams.
    EDA Tools
    • Altium Designer (expert level – schematic entry, PCB layout, DRC).
    • Knowledge of OrCAD, Allegro, Mentor Graphics (good to have).
    • Signal Integrity experience is a plus.
    Personal Skills
    • Strong team player, willing to share knowledge and support others.
    • Self-motivated and able to handle projects independently.
    • Proactive in escalating issues with solutions.
    • Effective in vendor communication and cross-functional collaboration.
    • Strong communication skills with colleagues, partners, and customers.

    QARA Engineer

    Experience

    3 to 6 Years

    About SILMATES

    Silmates Pvt. Ltd. is a service provider in the medical equipment domain, working with offshore clients on:

    • New Product Development (NPD)
    • Sustenance Engineering
    • Testing & V&V
    • End-to-end (Concept to Market) product development
    Job Summary

    The QA/RA Engineer will manage quality assurance and regulatory affairs for medical products, including FDA queries, compliance, and product lifecycle support.

    Key Responsibilities

    Quality Assurance

    • Remediate medical device documentation as per quality guidelines.
    • Implement and maintain QMS (ISO 13485, FDA standards).
    • Handle NCRs, CAPAs, and root cause analysis.

    Regulatory Affairs

    • Assess regulatory impact of product design changes.
    • Prepare and submit documents for FDA, CE Mark, and other approvals.
    • Monitor regulatory changes and ensure compliance.

    Product Development Support

    • Provide QA/RA input during design and development.
    • Evaluate and classify medical device complaints (FDA/MDR).
    • Review and approve design documentation.
    • Ensure proper risk management practices.
    • Train engineering staff on QMS requirements.

    Documentation & Training

    • Maintain accurate QA/RA records.
    • Conduct staff training on regulatory and quality standards.

    Qualifications

    • Bachelor’s degree in Engineering, Biomedical, or Life Sciences.
    • 3–5 years’ experience in QA/RA (medical devices or pharma).
    • Strong knowledge of FDA regulations, ISO 13485, QMS.
    • Proven experience handling FDA queries.
    • Good communication (English, written & verbal).
    • Certification (CQE, CQA, RAC) – preferred.

    Benefits

    • Competitive salary & benefits package.
    • Growth and development opportunities.
    • Collaborative and innovative environment.