Clinical Quality & Safety Intern — Summer 2027

MiniMed Group; California; On-site; USD 35,000 - 62,000; Full time

Benefits offered by this job

Housing assistance

Relocation support

Educational programs

Job summary

MiniMed offers a summer internship for a Clinical Product Quality & Safety Intern in Northridge, CA. You will work full-time (40 hours/week) for 10-11 weeks, contributing to clinical safety, post-market activities, and quality documentation.

You may review complaints, assess reportability, analyze data trends, and develop onboarding materials while collaborating with cross-functional teams and subject matter experts.

Qualifications

• Pursuing a bachelor’s degree in nursing, biology, chemistry, physiology, biomedical engineering, public health or related field with an expected graduation Winter 2027 – Spring 2029.
• Or enrolled in an MD/DO program.

Responsibilities

• Review product complaint coding for consistency, clarity, usability, and clinical relevance.
• Support clinical assessments of complaint reports and reportability decisions under supervision.
• Characterize patient impact, device involvement, and potential safety concerns.
• Analyze complaint data to identify recurring issues and post-market trends.
• Prepare summaries, analyses, and recommendations for Quality and Medical Safety stakeholders.
• Develop product knowledge and onboarding materials on product use and quality processes.
• Collaborate with SMEs to validate content and maintain documentation per privacy and confidentiality rules.

Skills

Data analysis

Trend analysis

Data visualization

Writing

Collaboration

Problem solving

Attention to detail

Clinical documentation

Adverse event reporting

Quality systems

Education

Bachelor's degree in nursing or biology or related clinical/health sciences

MD/DO (for MD/DO track)

Tools

Excel

PowerPoint

Word

Job description

MiniMed offers a summer internship for a Clinical Product Quality & Safety Intern in Northridge, CA. You will work full-time (40 hours/week) for 10-11 weeks, contributing to clinical safety, post-market activities, and quality documentation.

You may review complaints, assess reportability, analyze data trends, and develop onboarding materials while collaborating with cross-functional teams and subject matter experts.