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Sr Device Engineer

Job in San Francisco, San Francisco County, California, 94199, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-03-06
Job specializations:
  • Engineering
    Biomedical Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 120000 - 150000 USD Yearly USD 120000.00 150000.00 YEAR
Job Description & How to Apply Below
Position: Sr Device Engineer I

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).
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