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Sr Device Engineer I

Gilead Sciences
Remote friendly (San Francisco Bay Area)
United States
$136,340 - $176,440 USD yearly
Other

Role Summary

We are seeking a highly skilled and proactive Senior Device Development Engineer to lead technical development efforts for parenteral drug-device combination products, including autoinjectors, prefilled syringes, and needle safety systems. This individual contributor role is ideal for an engineer with deep technical expertise, strong cross-functional collaboration skills, and a passion for delivering innovative, patient-centric solutions. The role may include oversight of contractors or matrixed resources but does not include direct people management.

Responsibilities

  • Lead technical development activities for combination products from concept through commercialization, ensuring robust design and performance.
  • Develop and execute design control documentation, including design inputs/outputs, verification, validation, and risk management.
  • Author and review technical reports and contribute to regulatory submissions (IND, NDA, etc.).
  • Collaborate cross-functionally with Regulatory, Quality, Clinical, and Manufacturing teams to align on development strategy and execution.
  • Support technology transfer to clinical and commercial manufacturing sites, including process development and troubleshooting.
  • Drive technical problem-solving, root cause analysis, and continuous improvement initiatives.
  • Represent the device development function in internal and external technical discussions, including with suppliers and partners.
  • Stay current with industry standards and regulatory expectations, including FDA, EMA, ISO 13485, ISO 14971, and cGMP.

Qualifications

  • Required: Doctorate OR Master’s and 4+ years of relevant experience OR Bachelor’s and 6+ years of relevant experience.
  • Preferred: Bachelor’s or Master’s degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering, or related field; Minimum of 6+ years (BS) or 4+ years (MS) of relevant experience in combination product development; Strong understanding of design control, risk management, and regulatory standards for combination products; Demonstrated ability to solve complex technical problems and contribute to strategic project decisions; Excellent communication and collaboration skills.

Education

  • Bachelor’s or Master’s degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering, or related field (or equivalent).