Intern - Analytical Operations - PDM at Gilead Sciences

Foster City, California, United States

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Not SpecifiedCompensation

InternshipExperience Level

InternshipJob Type

UnknownVisa

Pharmaceuticals, BiotechnologyIndustries

Requirements

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

Responsibilities

Learn and apply Liquid Chromatography (LC) technique and its application within CMC space
Research and identify suitable substitutes for PFAS additives used in LC
Develop and optimize alternative LC method conditions for real-world applications
Propose and devise a regulatory filing strategy for new backup LC methods
Evaluate and recommend equivalent LC buffers and additives for direct substitution, ensuring performance parity
Analyze data and document findings for method development
Support the preparation of technical reports and regulatory documentation
Showcase your work with a final presentation (PPT) near the conclusion of your internship

Skills

Key technologies and capabilities for this role

Liquid ChromatographyLCCMCPFASAnalytical ChemistryMethod DevelopmentRegulatory Filing

Questions & Answers

Common questions about this position

What are the key responsibilities for this internship?

Key responsibilities include learning and applying Liquid Chromatography (LC) techniques, researching PFAS substitutes, developing and optimizing LC methods, proposing regulatory strategies, evaluating buffers and additives, analyzing data, supporting technical reports, and presenting final work.

What are the required qualifications for the Gilead intern position?

Candidates must be at least 18 years old, have a minimum GPA of 2.8, be authorized to work in the US without sponsorship or via CPT/OPT, currently enrolled full-time in a Bachelor's/Masters/MBA/PhD program at an accredited US university, rising Sophomore/Junior/Senior or graduate/doctoral student, enrolled full-time in Fall after internship, and able to complete a 10-12 week internship between May and August.

Is this a paid internship, and what is the compensation?

This information is not specified in the job description.

What is the duration and timing of the internship?

The internship is full-time for 10-12 consecutive weeks between May and August.

What opportunities does the Gilead internship offer beyond the main project?

Interns will participate in professional development and leadership presentations, social/network building activities, and local community volunteer programs, while contributing to high-impact projects and gaining real-world experience.

Gilead Sciences

Develops and commercializes biopharmaceuticals

About Gilead Sciences

Gilead Sciences focuses on discovering, developing, and commercializing medicines for various medical conditions, including HIV/AIDS, liver diseases, cancer, inflammatory and respiratory diseases, and cardiovascular issues. The company conducts extensive research and development to create new therapies, which are then marketed to healthcare providers, hospitals, and pharmacies after receiving regulatory approval. Gilead differentiates itself from competitors through its strong commitment to R&D and strategic partnerships, such as with SAP Ariba, to enhance its operations and product offerings. The company's goal is to improve health equity and access to care globally, working with communities to ensure that its medicines reach those in need.

Foster City, CaliforniaHeadquarters

1987Year Founded

$15,873.6MTotal Funding

IPOCompany Stage

Biotechnology, HealthcareIndustries

10,001+Employees

Benefits

Paid family time off and paid parental time off

Generous 401(k) contribution matching

Comprehensive medical plans that cover both physical and mental healthcare

Global Wellbeing Reimbursement

Time Off

Global Volunteer Day

Giving Together Program

Employee Support Programs

Flexible Work Options

Risks

Increased competition in HIV treatment from ViiV Healthcare's expanding drug portfolio.

Regulatory scrutiny over drug pricing could impact Gilead's U.S. market operations.

Patent expirations, like Truvada's, lead to increased generic competition and revenue loss.

Differentiation

Gilead's lenacapavir is recognized as the 2024 Breakthrough of the Year for HIV care.

Partnerships with LEO Pharma and Tubulis enhance Gilead's focus on inflammatory and cancer therapies.

Gilead's commitment to health equity initiatives like COMPASS and HepConnect sets it apart.

Upsides

Gilead's strategic partnerships expand its reach in inflammatory and oncology drug markets.

Investment in digital health technologies enhances Gilead's R&D and patient engagement.

Focus on sustainability improves Gilead's operational efficiency and corporate reputation.

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