Quality System Coordinator Intern at Intuitive Surgical, Inc. in Sunnyvale, California

Job Description:

Joining Intuitive Surgical means joining a team dedicated to using technology to benefit patients by improving surgical efficacy and

decreasing surgical invasiveness, with patient safety as our highest priority.

Eligibility:

Must beconcurrently enrolled and returning to an academic program in the fall in anaccredited degree-seeking program.

PrimaryFunction of Position:

The QualitySystems Coordinator will assist Quality System Staff Engineers in ensuringoverall Quality Management System (QMS) compliance to internalprocess/procedures as well as regulatory requirements/standards. S/He will useQuality System principles, tools and techniques to assist in the development,optimization, and support systems and processes that are aligned with theoverall Company strategy and mission affecting continuous process improvement. Tocomplete work projects to close identified gaps in the Quality System organization.

Rolesand Responsibilities:

• Complete gapassessment for regulations, regulatory standards, and corporate procedures


• Assist in review ofprocedures and approval of Engineering Change Orders


• Provide data tosupport; process analysis, process controls, FDA trending and finding history,and needed process improvements activities


• Provide support inidentification and implementation of continuous process improvements for documentationcontrol department


• Ensure quality systemsrecords are maintained according to requirements


• Participation in theupdating and review of global quality system documentation to meet new templaterequirements


• May perform as a teammember in internal audits

Skills, Experience,Education, & Training:

• Current enrollment inan Science, Technical writing or technical related field degree-seeking programat the Bachelor's level


• Completion of 3 yearsof coursework


• Excellentcommunication and technical writing skills


• 2 years of CollegeResearch or Laboratory experience


• Prefer completion ofTechnical Writing courses


• Ability to becomeproficient in FDA and ISO Medical Device Regulations


• Key Competency Areas: Communication,Time Management Skills, Collaboration, Process and Data Analysis, Technical Acumen,Ability to work independently

Gainunderstanding of Medical Device Regulations

Gain projectmanagement strategies and process experience

Gainexperience in building quality processes for medical device products

Commitment: Must be available to work full-timehours, M-F for 10-12 weeks beginning Summer of 2021.

We are an AA/EEO/Veterans/Disabled employer.

We will consider for employment qualified applicants with arrest and conviction records in accordance with fair chance laws.