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Quality Assurance Associate at Gilead Sciences - ApplyBlast

Quality Assurance Associate

Gilead Sciences

2 months ago

3.5 on Glassdoor

Foster City, California, United States

Onsite

Full Time

Medior

0 applicants

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About this role

The role supports QA oversight of clinical small molecule drug substance and oral solid dosage pilot plant manufacturing, including review and approval of manufacturing documentation, maintenance of quality records, and participation in investigations and process improvement projects. The associate works within a GMP environment, collaborates with cross‑functional teams, and contributes to regulatory inspections and internal audits.

Responsibilities

Support QA oversight of clinical small molecule drug substance manufacturing and disposition
Review and approve manufacturing documentation including batch records and deviation reports
Support regulatory inspections, internal audits, and preparation of audit responses

Skills

Qualifications

BSMS

About Gilead Sciences

gilead.com

Headquarters

Foster City, California, United States

Company Size

10001+ employees

Founded

1987

View Profile

Gilead Sciences is a biopharmaceutical company dedicated to transforming patient care by advancing therapeutics in areas like HIV, liver disease, cancer, and inflammation. With a strong commitment to innovation, Gilead leads in the research and development of new medicines, aiming to make the world a healthier place. Their portfolio includes breakthrough therapies and ongoing advancements across multiple therapeutic areas, supported by a robust pipeline of clinical trials. Gilead is recognized for its contributions to public health and its efforts to improve access to vital medications.