Engineer, R&D

Spyglass PharmaAliso Viejo, CA
$90,000 - $110,000

About The Position

We are seeking an Engineer I, R&D to contribute to the development of innovative ophthalmic medical devices at SpyGlass Pharma. This role is responsible for executing engineering activities including experimental design, device testing, and technical problem-solving with moderate independence. The Engineer I will collaborate closely with senior engineers and cross-functional teams to support product development from concept through validation.

Requirements

  • Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, or related engineering discipline.
  • 1–3 years of experience in medical device development or a related engineering field; equivalent combination of advanced degree, or relevant internship experience will be considered.
  • Solid understanding of engineering principles and laboratory practices relevant to medical device development.
  • Hands-on experience with laboratory testing, equipment, and data analysis.
  • Demonstrated ability to contribute to troubleshooting and problem-solving in device development.
  • Strong written and verbal communication skills, with the ability to clearly document and present technical information.
  • Ability to work both independently and collaboratively in a cross-functional team environment.

Nice To Haves

  • Familiarity with FDA design controls, ISO 13485, and risk management principles (ISO 14971) is preferred.

Responsibilities

  • Apply engineering principles to design and execute experiments and support method development for device engineering initiatives.
  • Troubleshoot device-related technical issues and contribute to solutions for development and laboratory challenges.
  • Collaborate with senior engineers to address device engineering problems of moderate complexity.
  • Support project execution and coordination, ensuring assigned deliverables and milestones are completed on schedule.
  • Document experimental results and prepare technical reports related to device performance, testing, and development activities.
  • Participate in design verification and validation activities, including development and execution of test protocols and data analysis.
  • Maintain accurate documentation in compliance with design control and Good Documentation Practices (GDP).
  • Collaborate cross-functionally with R&D, Quality, Regulatory, and Manufacturing teams to support development objectives.
  • Follow laboratory safety guidelines and ensure adherence to company policies and procedures.

Benefits

  • We are offering a range of $90,000 - $110,000, based on experience and qualifications, along with an Annual Bonus opportunity.
  • Share in our success with stock options, giving you a stake in the company’s future.
  • Comprehensive health, dental, and vision insurance plans to keep you and your family healthy and happy, with a variety of plan and coverage options.
  • Generous paid time off, including holidays, vacation days, and personal leave.
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