Intern – Global Quality Control Biologics (Lifecycle Management)
Location: Foster City, California, United States
Work Type: Full-Time | Onsite Required
Job ID: R0048745
Application Deadline: December 19, 2025
Posted: 15 Days Ago
Gilead Sciences is a global biopharmaceutical leader dedicated to advancing therapies for HIV, viral hepatitis, COVID-19, cancer, and other serious diseases. For over 35 years, Gilead has focused on innovation, patient access, and global health impact. This internship provides hands-on experience in Quality Control (QC) Biologics, supporting the lifecycle management of therapeutic products while contributing to high-impact projects in a fast-paced, collaborative environment.
Role Overview
The Intern – Global Quality Control Biologics (Lifecycle Management) will assist in documenting and optimizing QC processes across the biologics product lifecycle. This includes method validations, transfers, reference standard and critical reagent management, and QC product lead responsibilities. The role provides exposure to cross-functional teams and regulatory compliance in a real-world pharmaceutical setting.
Key Responsibilities
Research and document QC product lifecycle activities, including method validation, specification establishment, and critical reagent management.
Conduct interviews with Subject Matter Experts (SMEs) in QC and related departments to gather process insights and identify operational challenges.
Develop visual aids such as flowcharts, timelines, and checklists to enhance the usability of QC handbooks.
Draft, edit, and organize handbook content in a clear and consistent format.
Ensure alignment with internal quality standards and regulatory requirements.
Incorporate stakeholder feedback and iterate on handbook drafts.
Present progress updates and a final project presentation summarizing contributions at the conclusion of the internship.
Required Qualifications
Minimum age: 18 years
Minimum GPA of 2.8
Authorized to work in the U.S. without sponsorship or eligible through CPT/OPT
Full-time enrollment in a Bachelor’s, Master’s, MBA, or PhD program at an accredited U.S. university or college
Rising Sophomore, Junior, Senior, or Graduate/Doctoral student
Enrollment in the Fall semester following the internship
Ability to complete a 10–12 week consecutive internship between May and August
Willingness to relocate and work onsite for the duration of the internship
Preferred Qualifications
Degree focus: Undergraduate, Graduate, or PhD in life sciences, biotechnology, or a related field
Proficiency in Microsoft Office Suite (Excel, PowerPoint, Word)
Strong analytical, problem-solving, and organizational skills
Ability to work independently and collaboratively
Commitment to diversity, inclusion, and professional integrity
Familiarity with quality control concepts, method validation/qualification, and regulated environments (pharma, biotech, or manufacturing)
Experience Required
0–1 year of academic or internship experience in laboratory research, quality control, or regulatory-related projects
Exposure to pharmaceutical or biotechnology workflows is a plus
Practical experience using MS Office for reporting and data visualization
Compensation and Benefits
Hourly Range: USD 19.00 – USD 55.00
Actual compensation may vary based on education level and geographic location
Benefits include paid company holidays, sick time, and housing stipends for eligible interns
Gilead Core Values
Integrity (Doing What’s Right)
Inclusion (Encouraging Diversity)
Teamwork (Working Together)
Excellence (Being Your Best)
Accountability (Taking Personal Responsibility)
Equal Employment Opportunity
Gilead Sciences is committed to fostering an inclusive work environment and providing equal employment opportunities. Employment decisions are made without discrimination based on protected characteristics in accordance with federal, state, and local laws. Reasonable accommodations are available for applicants during the hiring process.
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