New · posted Oct 23
Gilead Sciences · Pharmaceuticals
Quality Control Specialist III
- La Verne, CA
- On-site
- Full-time
- Senior & Principal
Open until filled
The 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
At Gilead our pursuit of a healthier world for all people has yielded a cure for hepatitis C, revolutionary improvements in HIV treatment and prevention as well as advancements in therapies for viral and inflammatory diseases and certain cancers.
We set and achieve bold ambitions in our fight against the world’s most devastating diseases, united in our commitment to confronting the largest public health challenges of our day and improving the lives of patients for generations to come. As a QC Specialist III at Gilead, you will support Quality Control laboratory operations through the administration, enhancement, integration, and continuous improvement of QC computerized systems and digital solutions. You will also serve as a technical resource for laboratory informatics, instrumentation software, data analytics, system lifecycle management, and digital transformation initiatives. This role collaborates cross-functionally to implement innovative technologies that improve data integrity, compliance, operational efficiency, and laboratory productivity in a GMP-regulated environment.
This is a site-based position (Monday- Friday) in La Verne, CA.
What you need
Two ways to qualify
Bachelor’s
+ 5+ years of experience
5+ years of relevant experience and a BS or BA OR
- or
Master’s
+ 3+ years of experience
3+ years of relevant experience and a MS
Specific Education & Experience Requirements
Knowledge
- Strong understanding of laboratory informatics, computerized systems, and digital technologies.
- Experience with laboratory applications including LIMS, ELN, instrumentation software, and data visualization tools.
- Knowledge of AI, automation, digitalization, and emerging technologies applicable to pharmaceutical Quality Control laboratories.
- Experience developing, modifying, or utilizing scripts, queries, or code to automate laboratory processes, transform data, generate metrics, or integrate laboratory systems is preferred.
- Working knowledge of GMPs, GLPs, Data Integrity (ALCOA+), 21 CFR Part 11, Annex 11, and applicable regulatory requirements.
- Understanding of computerized system lifecycle concepts including validation, qualification, change management, and periodic review.
- Knowledge of analytical instrumentation and laboratory workflows.
- Strong project management, prioritization, and problem-solving skills.
- Excellent technical writing, communication, and interpersonal skills.
- Proficiency in Microsoft Office applications, data analytics, and reporting tools.
- Experience with system integration and data connectivity between laboratory instruments and enterprise systems is preferred.
Gilead's People Leader Accountabilities
- Create Inclusion - knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way they manage their teams.
- Develop Talent - understand the skills, experience, aspirations and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow, develop and realize their purpose.
- Empower Teams - connect the team to the organization by aligning goals, purpose, and organizational objectives, and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem.
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*.
Preferrednice to have
- Prior experience in pharmaceutical industry is preferred
- QC laboratory operations experience across: administration, enhancement, integration, and continuous improvement of QC computerized systems and digital solutions strongly preferred
What you'll do
Specific Job Responsibilities
- Provide technical troubleshooting and support for laboratory instrumentation and computerized systems.
- Identify process improvement opportunities and recommend solutions to enhance performance, compliance, and user experience.
- Interact with vendors to evaluate technologies, resolve technical issues, and support implementation activities.
- Monitor industry trends, emerging technologies, and best practices related to laboratory digitalization and QC informatics.
- Support computerized system validation activities including URS, risk assessments, test protocols, reports, and lifecycle documentation.
- Ensure systems remain compliant with applicable regulatory and data integrity requirements.
- Participate in change controls, deviations, CAPAs, periodic reviews, and audits.
- Support qualification and requalification activities for laboratory instrumentation and computerized systems.
- Partner with IT, Quality, and business stakeholders to identify and implement technology improvements.
- Drive adoption of innovative technologies including automation, artificial intelligence, advanced analytics, and digital workflows.
Pay
$107,185 – $138,710 a year
Employer providedFor additional benefits information, visit:
* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.
Where you'll work
La Verne, CAOn-siteOpen in Maps (opens in a new tab)
More jobs in La Verne, CAWorking conditions
For Current Gilead Employees and Contractors
Please apply via the Internal Career Opportunities portal in Workday.
Equal opportunity, accessibility and legal noticesGilead Sciences's statements, word for word
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 [email protected] 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.
Job intelligence
The context around this role
Live data · October 23, 2026
Salary intelligence
How the pay compares
This role's midpoint is 29% above the US median for Quality Control roles at this level.
This roleEmployer provided
Senior & Principal roles in California6 roles publishing pay
Senior & Principal roles in the US56 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $107,185 | — | $138,710 |
| California (middle half) | $95,500 | $106,750 | $121,750 |
| All US (middle half) | $78,500 | $95,500 | $113,125 |
This role: Gilead Sciences's own published range. Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, October 23, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Control
The general path across 324 open Quality Control roles on Regulatory Jobs, with the titles they carry most. Not Gilead's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 36 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Lab testing and methods12
- Data and digital systems12
- Collaboration and leadership12
- Quality systems and risk5
- GMP and compliance4
- Validation and qualification3
- Documentation and SOPs2
- Investigations and CAPA1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
- FDA21 CFR Parts 210 and 211(official source, opens in a new tab)FDA current good manufacturing practice for finished pharmaceuticals
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- FDAFDA data integrity guidance(official source, opens in a new tab)Data Integrity and Compliance With Drug CGMP: Questions and Answers
- European CommissionEU GMP (EudraLex Volume 4)(official source, opens in a new tab)The EU's good manufacturing practice rules and annexes
From Regulatory News
Manufacturing and quality coverage for this professionCompany hiring pulse
Gilead on Regulatory Jobs
- 40
- Open roles
- 35
- Distinct roles
- 6
- Locations
By discipline
- Quality29 73%
- Regulatory11 28%
By level
- Director16 40%
- Manager10 25%
- Senior & Principal10 25%
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Quality Control Specialist III at Gilead
Open until filled. $107K–$139K a year, employer provided.