Otsuka Pharmaceutical Companies (U.S.)→
Manufacturing Engineering Summer Intern at Otsuka… · Palo Alto
InternshipOn-sitePalo Alto$42k–$52k/yr
Skills
medical device manufacturingcleanroom environmentmicrosoft officefda regulationscad - solidworksstatisticsstatistical software - rstatistical software - minitabstatistical software - jmptest method validationgage r&rquality management system (qms)document change order (dco) processoperate independentlyaction orientationresult orientation
Job Description
Summary: Recor Medical is pioneering Ultrasound Renal Denervation therapy to treat hypertension. They are seeking a proactive Summer Intern for their Manufacturing Engineering team to support critical projects related to the development and quality of their technology, gaining hands-on experience in a regulated medical device environment.
Responsibilities:
- Collaborate with cross‑functional teams (Manufacturing, Quality, Engineering) to support process changes and continuous improvement initiatives
- Design or modify fixtures and order parts
- Develop, characterize and optimize process parameters using statistical techniques
- Write test protocols, execute studies and document results in test reports
- Perform Test Method Validations, Gage R&Rs, and other manufacturing studies, as needed
- Capture document changes through DCO (Document Change Order) process in a Quality Management System (QMS)
- Plan, schedule, and coordinate part of a project or a total project with a final project presentation
Required Qualifications:
- Undergraduate full-time student with at least 2 years completed, pursuing a degree in Mechanical Engineering, Bioengineering or similar
- Comfortable working in a cleanroom environment
- Proficiency in Microsoft Office suite
- Excellent verbal communication and technical writing skills
- Ability to operate independently and in a team
- Self-motivated, action oriented and result oriented
- Interns are expected to work onsite at the Palo Alto office five days a week throughout the 12‑week internship period
Preferred Qualifications:
- Familiarity with the following a plus: FDA Regulations
- Familiarity with the following a plus: CAD (SolidWorks)
- Familiarity with the following a plus: Statistics and Statistical software (R, Minitab, JMP)
Required Skills: Medical Device Manufacturing, Cleanroom Environment, Microsoft Office, FDA Regulations, CAD - SolidWorks, Statistics, Statistical Software - R, Statistical Software - Minitab, Statistical Software - JMP, Test Method Validation, Gage R&R, Quality Management System (QMS), Document Change Order (DCO) Process, Operate Independently, Action Orientation, Result Orientation