Hybrid Quality Intern: Biopharma Training & Mentorship

Travere Therapeutics; San Diego (CA); Hybrid; USD 34,000 - 48,000; Full time

Benefits offered by this job

Medical, dental, and vision coverage

Job summary

Travere Therapeutics invites applicants for an 11-week Early Career Talent Internship in Quality, based in San Diego. The intern will gain hands-on exposure to pharmaceutical quality systems, supporting document control and training (including LMS) while collaborating with cross-functional teams in a regulated environment.

The program offers mentorship, cross-functional exposure, and a final presentation to senior leadership detailing project work and learnings.

Qualifications

• Must be enrolled in an undergraduate program with at least one semester to complete before graduation.
• Interest in biotechnology, pharmaceutical quality, regulated operations, or compliance is preferred.

Responsibilities

• Participate in structured training to learn foundational concepts, processes, and systems used within the Quality organization.
• Support entry-level administrative activities and defined project work that contributes to Quality team priorities.
• Assist with organizing information, documentation, tracking, or other project support activities as assigned.
• Observe how quality systems support compliant and effective biopharmaceutical operations.
• Interview and interact with various quality functions and other departments to understand how aspects of the company interact to help ensure a compliant quality system.
• Document key learnings, contributions, and observations throughout the internship.
• Prepare and deliver a final presentation summarizing the project work completed, contributions made, and key aspects of Quality learned during the internship.

Skills

Attention to detail

Organization

Professional communication

Education

Undergraduate student

Job description

Travere Therapeutics invites applicants for an 11-week Early Career Talent Internship in Quality, based in San Diego. The intern will gain hands-on exposure to pharmaceutical quality systems, supporting document control and training (including LMS) while collaborating with cross-functional teams in a regulated environment.

The program offers mentorship, cross-functional exposure, and a final presentation to senior leadership detailing project work and learnings.