QA Specialist III

gilead· 1010 Gilead Sciences, Inc.
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📍 United States - California - La VerneFull time💰 USD 107K–139K
Full timeOnsite Required1010 Gilead Sciences, Inc.

About this role

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
 

Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.
 

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.

Job Description
 

A computer science background is required, along with hands-on experience in backend development and coding practices.

Roles/Responsibilities:

  • Serve as a Quality SME for SAP QM and Digital Quality solutions translating GMP business needs into system requirements and process improvements

  • Support SAP QM incident management, sustainment, and solution releases

  • Drive standardization and optimization of quality processes (e.g., material status, usage decision, jurisdictional control)

  • Partner cross‑functionally with Quality, Manufacturing, Supply Chain, and IT

  • Support global deployments through testing, change management, documentation, and training

  • Contribute to continuous improvement and KPI‑based performance monitoring

  • Performs a wide variety of activities to ensure compliance with applicable regulatory requirements.

  • Participates in developing Standard Operating Procedures to ensure quality objectives are met.

  • May facilitate external audits/inspection processes as SAP SME, supporting implementation of corrective actions as needed.

  • May assist with compliance audits as required.

Basic Qualifications:

  • 6+ years of relevant experience in a GMP environment related field and a BS or BA. (computer science)

  • 4+ years of relevant experience and an MS.

  • Prior experience in pharmaceutical or biopharmaceutical industry.

  • Strong GMP and Quality Systems knowledge

  • Familiarity with MES, LIMS (or GLIMS), and document management systems

  • Demonstrates strong verbal, technical writing and interpersonal skills.

  • Demonstrates proficiency in Microsoft Office applications.

  • SAP system development, coding and/or validation.

  • A computer science background is required, along with hands-on experience in backend development and coding practices.


 

The salary range for this position is: $107,185.00 - $138,710.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.

For additional benefits information, visit:

https://www.gilead.com/careers/compensation-benefits-and-wellbeing

* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.


For jobs in the United States:

Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact ApplicantAccommodations@gilead.com for assistance.


For more information about equal employment opportunity protections, please view the 'Know Your Rights' poster.

NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT
YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT


Gilead Sciences will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the  legal duty to furnish information; or (d) otherwise protected by law.
 

Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.


Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.


For Current Gilead Employees and Contractors:

Please apply via the Internal Career Opportunities portal in Workday.

Frequently Asked Questions

What is the salary for the QA Specialist III role at gilead?
The listed salary for this QA Specialist III position at gilead is USD 107K–139K. This is an Full time role.
Where is the QA Specialist III position at gilead located?
This QA Specialist III role at gilead is based in United States - California - La Verne. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the QA Specialist III role at gilead full-time or part-time?
This is listed as a Full time position. It is posted as a QA Specialist III role in the 1010 Gilead Sciences, Inc. department at gilead.
Which team or department does the QA Specialist III at gilead belong to?
This QA Specialist III position is part of the 1010 Gilead Sciences, Inc. department at gilead. See the full job description for more information about the team structure and responsibilities.
How do I apply for the QA Specialist III position at gilead?
Click the "Apply Now" button on this page. You will be redirected to gilead's official application portal hosted on workday where you can submit your application directly.
QA Specialist III
gilead · 💰 USD 107K–139K
Apply for this role ↗

You'll be redirected to gilead's official application page on Workday.