R&D Engineering Intern

Spyglass PharmaAliso Viejo, CA
1d$28

About The Position

We are seeking a hands-on R&D Engineering Intern to join our team at SpyGlass Pharma. The R&D Engineering Intern will primarily support the engineering team through sample builds, laboratory testing, and general engineering project support activities. This role offers direct exposure to the development of innovative ophthalmic drug delivery and implantable technologies in a regulated medical device and pharmaceutical environment. The intern will work closely with engineers and cross-functional partners to help execute prototype builds, generate test data, and maintain high-quality documentation in accordance with design control and quality system requirements.

Requirements

  • Currently pursuing a Bachelor’s or Master’s degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering, or a related engineering discipline.
  • Strong interest in medical device and/or pharmaceutical product development.
  • Basic understanding of engineering fundamentals, including mechanics, materials, or manufacturing processes.
  • Strong analytical and problem-solving skills.
  • Excellent written and verbal communication skills.
  • Ability to work collaboratively in a fast-paced, team-oriented environment.
  • Detail-oriented with strong organizational skills.

Nice To Haves

  • Familiarity with CAD software (e.g., SolidWorks or similar) preferred.

Responsibilities

  • Support engineering sample builds, including component preparation, assembly, inspection, and documentation.
  • Perform hands-on laboratory testing and bench evaluations of prototypes and development samples.
  • Collect, organize, and analyze test data to support feasibility, verification, and process development activities.
  • Assist engineers with troubleshooting build and test issues, identifying root causes, and implementing improvements.
  • Maintain accurate documentation, including build records, test protocols, data sheets, and summary reports in accordance with Good Documentation Practices (GDP).
  • Assist in the preparation of engineering drawings, work instructions, and test methods as needed.
  • Provide general engineering team support, including organizing materials, maintaining lab equipment, and ensuring workspaces comply with safety and quality standards.
  • Collaborate with cross-functional teams including Pharmaceutical Development, Quality Assurance, and Manufacturing to support development initiatives.
  • Follow laboratory safety guidelines and comply with company policies and procedures.
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