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Staff Software Quality Engineer – Product Development

Illumina
Bengaluru, IND
Full-time
Senior · 8+ years experience
Onsite
Discovered 3 weeks ago
Communication

Full Job Posting

Preferred Education:

  • Bachelor’s degree in Computer Science, Software Engineering, Bioinformatics, Biomedical or related discipline
  • Job Requirements:
  • 8+ years of experience in software quality engineering, software development, systems engineering, or a related discipline within a regulated industry.
  • Working knowledge of applicable regulations and standards, including IEC 62304, ISO 13485, QMSR, FDA regulations, and software risk management practices.
  • Strong understanding of software verification, validation, risk management, cybersecurity, and quality system requirements.
  • Experience supporting regulated software products, including Software as a Medical Device (SaMD), cloud-based software solutions, or complex software-enabled systems.
  • Demonstrated ability to influence technical and business decisions without direct authority.
  • Experience leading complex cross-functional initiatives involving multiple stakeholders.
  • Experience mentoring engineers or cross-functional partners on software quality practices and regulatory expectations.
  • Strong analytical, problem-solving, and decision-making skills.
  • Excellent verbal and written communication skills with the ability to communicate effectively across technical and non-technical audiences.
  • Experience supporting internal and external regulatory inspections and audits preferred.
  • Quality and/or Regulatory Certifications (ASQ, AAMI, RAPS, etc.) preferred.
  • Occasional travel may be required.
  • Willingness to work in shifts to support the US region (No night shift required).

Qualifications

  • Bachelor’s degree in Computer Science, Software Engineering, Bioinformatics, Biomedical or related discipline
  • 8+ years of experience in software quality engineering, software development, systems engineering, or a related discipline within a regulated industry.
  • Working knowledge of applicable regulations and standards, including IEC 62304, ISO 13485, QMSR, FDA regulations, and software risk management practices.
  • Strong understanding of software verification, validation, risk management, cybersecurity, and quality system requirements.
  • Experience supporting regulated software products, including Software as a Medical Device (SaMD), cloud-based software solutions, or complex software-enabled systems.
  • Demonstrated ability to influence technical and business decisions without direct authority.
  • Experience leading complex cross-functional initiatives involving multiple stakeholders.
  • Experience mentoring engineers or cross-functional partners on software quality practices and regulatory expectations.
  • Strong analytical, problem-solving, and decision-making skills.
  • Excellent verbal and written communication skills with the ability to communicate effectively across technical and non-technical audiences.
  • Experience supporting internal and external regulatory inspections and audits preferred.
  • Quality and/or Regulatory Certifications (ASQ, AAMI, RAPS, etc.) preferred.
  • Occasional travel may be required.
  • Willingness to work in shifts to support the US region (No night shift required).

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