New · posted Oct 14
Gilead Sciences · Pharmaceuticals
Director, QC Technology & Innovation
- La Verne, CA
- On-site
- Full-time
- Director
Open until filled
The role
The Director, QC Technology & Innovation reports to the Site QC Head and provides scientific and technical leadership for QC technology, analytical methods, method transfer, and laboratory innovation.
This role is responsible for driving the adoption and implementation of new instruments, testing technologies, digital solutions, and automation, while strengthening the scientific understanding and robustness of analytical methods. The Director will also lead analytical method transfers and complex technical troubleshooting to ensure QC capabilities evolve with the site’s portfolio and business needs.
The role will advance QC toward a highly automated, digitally integrated, and low-touch laboratory environment, leveraging emerging analytical technologies, automation, robotics, and innovative testing approaches.
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
2. Method Transfer & New Product Introduction
- Lead analytical method transfers supporting new product introduction, PPQ, commercial manufacturing, and product lifecycle changes.
- Assess method readiness, technical risks, instrumentation requirements, laboratory capability, and training needs.
- Provide technical leadership for method validation, verification, transfer, and implementation.
- Partner closely with MSAT, QA, Regulatory CMC, Manufacturing, and sending units to ensure successful method transfer.
- Ensure transferred methods are scientifically sound, robust, and suitable for routine GMP testing.
3. Analytical Science & Technical Troubleshooting
- Serve as a senior technical expert for analytical methods, testing technologies, and laboratory instrumentation.
- Lead resolution of complex analytical, method, and instrument-related issues.
- Provide technical leadership for complex laboratory investigations, including OOS/OOT and method performance issues.
- Apply science-based problem solving and experimental design to identify root causes and develop sustainable solutions.
- Strengthen scientific understanding, critical thinking, and technical problem-solving capability across QC.
4. QC Capability & Continuous Improvement
- Assess future analytical and technology needs across small molecule and biologics portfolios.
- Identify capability gaps and develop solutions related to instrumentation, methods, technology, and technical expertise.
- Drive continuous improvement of analytical methods and laboratory technologies.
- Establish appropriate metrics for method transfer, technology implementation, and technical performance.
- Build technical capability through coaching, knowledge sharing, and development of subject matter experts.
What you need
3 ways to qualify
Bachelor’s
+ 12+ years of experience
BS in a scientific discipline with 12+ years of relevant pharmaceutical/biopharmaceutical experience; or
- or
Master’s
+ 10+ years of experience
MS with 10+ years of relevant experience; or
- or
PhD
+ 8+ years of experience
PhD with 8+ years of relevant experience.
Required Education/Experience
- Significant experience in QC, Analytical Sciences, Analytical Development, or a related GMP laboratory function.
1. Technology & Innovation
- Lead implementation of the site QC technology and innovation strategy in collaboration with Global Quality, ensuring alignment with the Global Quality Digital and Innovation Strategy, enterprise priorities, and future-state vision.
- Collaborate with global and site stakeholders to identify, evaluate, and implement laboratory instruments, analytical technologies, automation, digital solutions, and testing approaches that align with global strategies and standards.
- Develop and maintain a future-state QC technology roadmap aligned with the global vision and roadmaps, progressively enabling automated, integrated, and low-touch testing across the network.
- Partner across site and global functions to identify opportunities to automate end-to-end analytical workflows, reduce manual interventions and handoffs, and improve data flow and testing efficiency in alignment with global process and digital strategies.
- Lead proof-of-concept studies and technical assessments for emerging technologies in collaboration with global subject matter experts, sharing outcomes to support coordinated investment and scalable adoption.
- Drive modernization and simplification of laboratory testing in alignment with the global quality vision, leveraging network standards, shared capabilities, and best practices to improve efficiency, reliability, and analytical capability.
- Strong technical expertise in QC analytical methods, laboratory instrumentation, and analytical technologies.
- Demonstrated experience in analytical method transfer, validation, implementation, and lifecycle management.
- Proven ability to lead complex technical troubleshooting and laboratory investigations using sound scientific principles.
- Experience evaluating and implementing new analytical technologies, automation, robotics, and digital laboratory solutions.
- Experience supporting commercial manufacturing, PPQ, and new product introduction in a GMP environment.
- Strong knowledge of GMP requirements, data integrity, and regulatory expectations for QC laboratories.
- Strong cross-functional leadership, communication, and problem-solving skills.
Preferrednice to have
- Advanced degree in a scientific discipline.
- Experience with both small molecule and biologics analytical technologies.
- Experience implementing advanced laboratory automation or innovative testing technologies.
The salary range for this position is: $191,250.00 - $247,500.00. 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*.
Pay
$191,250 – $247,500 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 14, 2026
Salary intelligence
How the pay compares
This role's midpoint is 11% above the US median for Quality Control roles at this level.
This roleEmployer provided
Director roles in California5 roles publishing pay
Director roles in the US18 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $191,250 | — | $247,500 |
| California (middle half) | $191,000 | $219,500 | $241,000 |
| All US (middle half) | $186,875 | $198,000 | $212,750 |
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 14, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Control
The general path across 189 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 43 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Lab testing and methods27
- Collaboration and leadership18
- Validation and qualification7
- GMP and compliance4
- Investigations and CAPA3
- Documentation and SOPs1
- Quality systems and risk1
- Data and digital systems1
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
- FDAFDA data integrity guidance(official source, opens in a new tab)Data Integrity and Compliance With Drug CGMP: Questions and Answers
- FDAFDA OOS guidance(official source, opens in a new tab)Investigating Out-of-Specification (OOS) Test Results for Pharmaceutical Production
- ICHICH quality guidelines(official source, opens in a new tab)Q1 stability, Q2(R2) analytical validation, Q7, Q9 risk management, Q10 quality systems
Company hiring pulse
Gilead on Regulatory Jobs
- 46
- Open roles
- 39
- Distinct roles
- 7
- Locations
By discipline
- Quality29 63%
- Regulatory16 35%
- Compliance & Safety1 2%
By level
- Associate & Specialist15 33%
- Director14 30%
- Manager9 20%
More roles at Gilead
- View role
Director, QC Product Readiness
Foster City, CADirectorPharmaceuticals$210K–$272K
- View role
Associate Director, Quality Control - Analytical Tech Services
Frederick, MDDirectorBiotechnology$165K–$214K
- View role
Senior Director, Quality Control (QC Head)
La Verne, CADirectorPharmaceuticals$221K–$286K
- View role
Intern - PDM - Quality Control (Method Validation)
Foster City, CA · HybridAssociate & SpecialistPharmaceuticals$42K–$114K
Similar Quality Control roles elsewhere
- View role
Associate Director, Quality Control
TakedaBrooklyn Park, MNDirectorPharmaceuticals$154K–$243K
- View role
Site QC Head (Associate Director)
NovartisIndianapolis, INDirectorPharmaceuticals$139K–$257K
- View role
Sr. Director - Quality Control Laboratories
Eli LillyHuntsville, ALDirectorPharmaceuticals$156K–$229K
- View role
Director, QC Automation
Bristol Myers SquibbDevens, MADirectorPharmaceuticals$185K–$246K
Director, QC Technology & Innovation at Gilead
Open until filled. $191K–$248K a year, employer provided.