Medical Domain Leader

15 years

0 Lacs

Posted:1 week ago| Platform: Linkedin logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Job Requirements

A domain leader with experience in the medical domain with a deep understanding of clinical laboratory processes, medical device technology, and relevant regulatory standards. He/She should lead development teams to build compliant, high-quality, and reliable software and systems that directly impact patient care and diagnostics.He/She will oversee the design, development, and implementation of complex software solutions for medical devices and clinical laboratory systems. This role requires a blend of hands-on technical expertise, strategic leadership, and a thorough understanding of medical standards and regulations. The ideal candidate will mentor a team of engineers, guide technical decisions, and collaborate with cross-functional teams to deliver innovative and compliant medical products.

Roles And Responsibilities

Technical leadership and architecture
  • Lead the design and development of software architecture for clinical lab and medical device products, ensuring scalability, performance, and security.
  • Provide technical guidance, conduct code reviews, and ensure adherence to best practices and coding standards.
  • Drive innovation by evaluating and integrating new technologies, frameworks, and methodologies relevant to the medical field.
  • Troubleshoot and resolve complex technical issues related to system architecture, software defects, and integrations.

Medical Domain Expertise

  • Clinical Laboratory Systems:
    • Oversee the development of software for laboratory information systems (LIS) and other lab-related platforms.
    • Ensure proper handling of clinical data, including sample tracking, test result reporting, and data management in compliance with regulations.
    • Integrate software with lab equipment, such as automated analyzers and PCR instrumentation, handling data acquisition and quality control.
  • Treatment Devices:
    • Lead software development for embedded systems and user interfaces in medical treatment devices.
    • Ensure the software for therapeutic devices meets strict safety, reliability, and usability requirements.
    • Apply knowledge of device-specific standards to the software design and testing processes.
  • Regulatory Standards:
    • Ensure all development processes and products comply with relevant medical standards and regulations, such as FDA guidelines, ISO 13485, IEC 62304, and HIPAA.
    • Oversee documentation for regulatory submissions, including design specifications, risk analysis, and validation protocols.
    • Participate in quality assurance processes and internal audits to maintain high standards and accreditation.
Team management and collaboration
  • Manage a technical team, including mentoring and training junior engineers, and conducting performance reviews.
  • Work closely with product managers, QA engineers, and clinical experts to translate requirements into effective technical solutions.
  • Communicate project status, technical risks, and progress to stakeholders, including both technical and non-technical audiences.
  • Foster a collaborative environment that promotes teamwork, quality, and continuous improvement.

Experience

Work Experience

  • 15+ years of experience in software development, with a minimum of 5+ years in a technical leadership or senior engineering role.
  • Proven experience in the medical domain, specifically with clinical laboratory systems or treatment devices.
  • Experience working within regulatory frameworks for medical devices and health information technology.

Technical Skills

  • Expertise in programming languages such as C++, C#, Java, or Python.
  • Deep understanding of software development life cycles (SDLC) and methodologies (e.g., Agile).
  • Proficiency in designing and building scalable, secure, and resilient software systems.
  • Experience with relevant technologies like laboratory information systems (LIS), Electronic Medical Records (EMR), and data analysis tools.

Domain Knowledge

  • Strong understanding of clinical laboratory workflows, data, and instrumentation.
  • Familiarity with medical device software development processes, risk management,

Soft Skills

  • Exceptional leadership, communication, and interpersonal skills.
  • Strong analytical and problem-solving abilities with high attention to detail.
  • Proven ability to work in a fast-paced, regulated, and collaborative environment

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