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Gilead Sciences · 1 day ago

Intern – Global Quality Control Biologics – Lifecycle Management

San Francisco Bay Area

Internship

Onsite

Intern

$19/hr - $55/hr

Gilead Sciences is a leader in developing therapies for serious diseases. The intern will contribute to high-impact projects related to quality control product lifecycle activities, gaining real-world experience while participating in professional development and community engagement activities.

BiopharmaBiotechnologyHealth CareManufacturingPharmaceutical

Comp. & Benefits

No H1B

Responsibilities

Research and document the full QC product lifecycle activities, including method validations and transfers, specification establishment, reference standard and critical reagent management, and the responsibilities of a QC product lead

Interview subject matter experts (SMEs) within QC and across departments to gather process details and pain points

Create visual aids such as flowcharts, timelines, and checklists to enhance handbook usability

Draft, edit, and organize handbook content in a clear and consistent format

Ensure alignment with regulatory requirements and internal quality standards

Incorporate feedback from stakeholders and iterate on handbook drafts

Present progress updates and final deliverables with a final presentation near the conclusion of your internship

Qualification

Quality Control conceptsMethod validationMS Office SuiteTeamworkCommitment to diversityProblem-solvingOrganizational skillsCollaboration

Required

Must be at least 18 years old

Must have a minimum GPA of 2.8

Authorized to work in the United States without Sponsorship now or in the future or CPT/OPT through your University

Must be currently enrolled as a full-time student in a Bachelor's/Masters/MBA/PhD program at an accredited US based university or college

Must be a Rising Sophomore, Junior, or Senior in undergrad or a Graduate or Doctoral Student

Must be enrolled full-time in the Fall Semester at an accredited university/college after the completion of the internship

Must be able to complete a 10-12 consecutive week internship between May and August

Must be able to relocate if necessary and work at the designated site for the duration of the internship

Preferred

Preferred Degree qualification: Undergrade/Graduate/PhD

Proficiency with MS Office Suite

Ability to identify issues and seek solutions

Ability to work both independently and collaboratively

Demonstrated commitment to inclusion and diversity in the workplace

Efficient, organized, and able to handle short timelines in a fast-paced environment

Show Teamwork/Collaboration

Familiarity with quality control concepts, method validation/qualification, or regulated environments (e.g., pharma, biotech, manufacturing) is a plus