INTERNSHIP DETAILS

Intern, Quality Compliance

CompanyMirum Pharmaceuticals
LocationFoster City
Work ModeOn Site
PostedMarch 10, 2026
Internship Information
Core Responsibilities
The intern will support the development and implementation of data dashboards to monitor and enhance vendor compliance across GxP-regulated activities, assisting in gathering, organizing, and analyzing compliance data to build meaningful visual reports. Responsibilities include completing GxP training, helping build and update compliance monitoring dashboards, reviewing data for trends, and supporting routine compliance report standardization.
Internship Type
full time
Company Size
427
Visa Sponsorship
No
Language
English
Working Hours
40 hours
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About The Company
Mirum Pharmaceuticals, Inc. is a biopharmaceutical company dedicated to transforming the treatment of rare diseases affecting children and adults. Mirum has three approved medications: LIVMARLI® (maralixibat), CHOLBAM® (cholic acid) capsules, and CTEXLI™ (chenodiol) tablets. LIVMARLI, an IBAT inhibitor, is approved for the treatment of two rare liver diseases affecting children and adults. It is approved for the treatment of cholestatic pruritus in patients with Alagille syndrome in the U.S. (three months and older), in Europe (two months and older), and in other regions globally. It is also approved in the U.S. in cholestatic pruritus in PFIC patients 12 months of age and older; in Europe, it is approved for patients with PFIC three months of age and older. Mirum is also initiating the Phase 3 EXPAND study, a label expansion opportunity for LIVMARLI in additional settings of cholestatic pruritus. CHOLBAM is FDA-approved for the treatment of bile acid synthesis disorders due to single enzyme deficiencies and adjunctive treatment of peroxisomal disorders in patients who show signs or symptoms of liver disease. CTEXLI is FDA-approved for the treatment of cerebrotendinous xanthomatosis (CTX) in adults. Mirum's late-stage pipeline includes two investigational treatments for several rare diseases. Volixibat, an IBAT inhibitor, is being evaluated in two potentially registrational studies including the Phase 2 VISTAS study for primary sclerosing cholangitis (PSC) and Phase 2b VANTAGE study for primary biliary cholangitis (PBC). Volixibat has been granted Breakthrough Therapy Designation for the treatment of cholestatic pruritus in patients with PBC. Mirum is also planning for a Phase 2 study evaluating MRM-3379, a PDE4D inhibitor for the treatment of Fragile X syndrome, a rare genetic neurocognitive disorder.
About the Role

 

MISSION

Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.

 

Position Summary

As an Intern within Mirum’s Quality Compliance Team, you will support the development and implementation of data dashboards designed to monitor and enhance vendor compliance across GxP-regulated activities (GCP, GMP, GDP, GLP, GCLP and/or GVP as applicable). This internship offers a structured learning opportunity to gain exposure to pharmaceutical quality systems and vendor oversight processes within a regulated environment.

Under the guidance of Quality Compliance leadership, you will assist in gathering, organizing, and analyzing compliance data from internal systems and tracking tools to help build meaningful visual reports and dashboards. You will learn how key performance indicators (KPIs) are used to assess vendor performance, identify trends, and support proactive quality oversight. This role will provide hands-on experience in data organization, basic analytics, and quality reporting while contributing to ongoing compliance initiatives.

  • This will be an 8-week assignment, 40 hours/week, paid internship
  • Housing costs will not be reimbursed.
  • Required to be on-site in Foster City, CA

Responsibilities And Main Tasks

  • Complete training on GxP regulations, internal quality systems (such as Veeva QMS/QDOC), and relevant company procedures
  • Work with the Quality Compliance team to understand how vendor performance is measured and tracked
  • Help build and update data dashboards that monitor vendor compliance activities (such as Audit Status, Findings and Audit CAPAs)
  • Review data to help identify trends, patterns, or potential compliance gaps
  • Assist with gathering and organizing data from quality systems and tracking tools to ensure accuracy
  • Support efforts to standardize and improve routine compliance reports
  • Help prepare materials and reports that support inspection readiness activities
  • Create simple documentation or user guides to explain how dashboards and reports are maintained
  • Provide general project and administrative support to the Quality Compliance team as needed

Minimum Requirements

  • Undergraduate or Graduate student in a scientific or related discipline.
  • Proficiency in Microsoft Office applications (Excel required; advanced Excel skills preferred)
  • Interest in data visualization tools (e.g., Power BI, Tableau, or similar platforms) preferred

Required Skills

  • Passion to learn
  • Ability to adopt urgent situations and accept ad hoc assignments
  • Demonstrated ability to prioritize tasks and meet deadlines.
  • Organized, responsible, resourceful, and detail-oriented
  • Strong written and oral communication skills
  • Ability to work effectively both independently and within a team.

Benefits For You

  • Gain meaningful professional experience in GxP Quality Compliance and vendor oversight
  • Gain cross-functional insight learning how to work within a global company
  • Working in a friendly environment with a collaborative spirit
  • Given an opportunity to improve personal growth and development

Please include your cover letter with your application outlining your desire to learn about this position.

#LI-ONSITE

Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.

Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.

Key Skills
Data DashboardsVendor ComplianceGxP RegulationsPharmaceutical Quality SystemsData AnalysisVisual ReportsKey Performance IndicatorsData OrganizationQuality ReportingVeeva QMS/QDOCAudit Status TrackingInspection ReadinessMicrosoft ExcelData VisualizationCommunication Skills
Categories
Science & ResearchData & AnalyticsHealthcareAdministrative
Benefits
Meaningful professional experience in GxP Quality Compliance and vendor oversightCross-functional insight learning how to work within a global companyWorking in a friendly environment with a collaborative spiritOpportunity to improve personal growth and development