The intern will work with our engineering and design team to characterize individual device components. These evaluations will address the physical, chemical, and structural characteristics of specific components.

Duties and responsibilities will include:

- Designing, preparing, and executing component evaluations utilizing both internal and external resources.

- Test, evaluate, and characterize individual device components

- Teat, evaluate, and characterize protocols for device component assembly and fabrication

- Perform product manufacturing for clinical materials according to standards. Includes assembling raw materials, following specific standard operating procedures (SOP), completing batch records, reporting deviations.

- Assists in the development of Standard Operating Procedures (SOPs) for manufacturing in collaboration with QMS lead.

- Maintain detailed documentation records and reports, SOPs, batch records and other materials to facilitate tech transfer, manufacturing, and regulatory submissions

- Participates in production activities and completes production batch records

Maintain a lab notebook, batch records/QC forms where necessary, and contribute to written reports and presentations

Note: Offsite is an option with a larger design focus

Encellin

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Medical Engineering - Encellin