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Viral Vector Jobs in California (NOW HIRING)

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Viral Vector information

See California salary details

$29.9K

$100.2K

$186.1K

How much do viral vector jobs pay per year?

As of Aug 11, 2026, the average yearly pay for viral vector in California is $100,177.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,629.00 and $132,685.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the viral vector position, and why are they important?

To excel as a Viral Vector Scientist, you typically need a strong background in molecular biology, virology, or related life sciences, often supported by a relevant advanced degree. Familiarity with laboratory techniques such as cloning, cell culture, qPCR, viral purification, and use of tools like flow cytometry and bioreactors is essential, with certifications in biosafety being advantageous. Strong attention to detail, problem-solving skills, and effective teamwork are key soft skills for success in this field. These competencies are crucial for ensuring the safe, efficient, and reliable development of viral vectors used in gene therapy and biomedical research.

What is a viral vector?

A Viral Vector job typically involves the development, production, and optimization of viral vectors used in gene therapy and vaccine applications. Professionals in this field work in biotechnology or pharmaceutical companies, focusing on designing and engineering viruses to deliver genetic material into cells safely and efficiently. Responsibilities may include cell culture, molecular cloning, vector purification, and quality control. This role is critical in advancing treatments for genetic disorders, cancer, and infectious diseases.

What are some common challenges faced by professionals working in viral vector development?

Professionals in viral vector development often encounter challenges such as troubleshooting low viral yields, maintaining strict contamination controls, and optimizing protocols for efficient gene delivery. The work environment is highly regulated, requiring close attention to safety and compliance standards, and frequent collaboration with cross-functional teams like quality assurance and manufacturing. Staying updated with emerging technologies and evolving regulatory requirements is also crucial. These challenges help foster advanced technical expertise and provide valuable problem-solving experience that contribute to long-term career growth in gene therapy and biotechnology.

Infographic showing various Viral Vector job openings in California as of August 2026, with employment types broken down into 73% Full Time, 21% Part Time, 2% Temporary, and 4% Contract. Highlights an 70% Physical, 5% Hybrid, and 25% Remote job distribution, with an average salary of $100,177 per year, or $48.2 per hour.

Exec Director, Viral Vector Process Development

Gilead

Santa Monica, CA • On-site

Full-time

Medical, Dental, Vision, Life, PTO

Re-posted 3 days ago


Gilead Sciences rating

8.9

Company rating: 8.9 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

9th of 86 rated pharmaceutical


Job description

We're here for one reason and one reason only - to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We've made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet.

Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next.

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 Kite and help create more tomorrows.


Job Description

This role is accountable for end-to-end viral vector development, from construct design through clinical and commercial manufacturing support, and serves as a key partner across Research, Product Teams, Technical Operations, and Analytical functions.

The leader will balance deep technical expertise with executive-level influence, ensuring robust, scalable vector platforms while building a high-performing organization capable of supporting both ex vivo and emerging in vivo applications.


Reporting & Location

  • Reports to: SVP, Global Head of Process Development
  • Location: Santa Monica, CA Or Oceanside, CA
  • On-site presence required

Key Responsibilities


Technical & Scientific Leadership

  • Accountable for technical strategy for viral vector platforms across clinical and commercial scale, including complex tech transfers, external manufacturing partnerships, and latestage manufacturing readiness.
  • Provide deep expertise in lentiviral vector (LVV) design, including construct architecture, promoter selection, and transgene optimization
  • Lead viral vector process development, including:
    • Upstream production systems (transient and stable)
    • Downstream purification and recovery operations
  • Drive process scale-up and technology transfer to clinical and commercial manufacturing sites (internal and external)
  • Oversee LVV life cycle management and manufacturing support capabilities
  • Lead initiatives to improve viral vector productivity, robustness, and cost of goods
  • Advance next-generation capabilities, including:
    • In vivo viral vector development
    • Platform innovations and emerging delivery technologies

Cross-Functional & Product Development Leadership

  • Ensure viral vector development decisions are optimized across the full cell therapy value chain, from transduction efficiency and cell performance to manufacturing robustness and CMC sustainability.
  • Provide strategic leadership for viral vector on cross-functional Product Teams
  • Partner closely with:
    • Research to translate early concepts into developable and scalable vector designs
    • T cell process development to align vector performance with cellular outcomes
    • Analytical development to ensure appropriate characterization and control strategies
  • Contribute to integrated product development, ensuring vector design and process decisions align with clinical and commercial objectives
  • Drive alignment across functions in a matrixed environment, balancing competing priorities while maintaining product focus

CMC & Regulatory Engagement

  • Strong working knowledge of cGMP regulations and compliance systems related to viral vector development, including inspection readiness, audit support, and direct engagement with regulatory agencies.
  • Contribute to LVV CMC strategies, including phase-appropriate viral vector development and scale-up approaches
  • Support regulatory filings and health authority interactions as a technical expert
  • Provide input into comparability strategies for process changes, site transfers, and lifecycle evolution of LVV

Organizational Leadership & Talent Development

  • Provide leadership oversight for viral vector development laboratories and GMPadjacent environments, ensuring facility readiness, compliance, and operational excellence in support of clinical and commercial programs.
  • Demonstrated experience leading large organizations within a highly matrixed cell and gene therapy environment.
  • Build, lead, and scale a high-performing viral vector development organization
  • Recruit, develop, and retain top scientific and leadership talent
  • Coach and develop future leaders, ensuring depth and succession within the organization
  • Foster a culture of:
    • Scientific rigor and accountability
    • Ownership and execution
    • Collaboration and transparency

Leadership, Communication & Executive Influence

  • Demonstrate strong executive presence, with the ability to clearly communicate complex technical concepts to diverse audiences
  • Influence decision-making at senior leadership and governance levels, providing clear, balanced perspectives on risks, trade-offs, and options
  • Drive clarity in ambiguity, enabling teams to make timely and well-informed decisions
  • Communicate effectively across:
    • Technical teams
    • Cross-functional stakeholders
    • Executive leadership
  • Build credibility as a trusted partner and advisor, both internally and externally
  • Represent the organization in external collaborations, partnerships, and industry forums

Basic Qualifications

  • PhD in Biochemical Engineering, Molecular Biology, Virology, or related field with 15+ years of experience (or MS with 18+ years)
  • Extensive experience in viral vector development and manufacturing support for cell and/or gene therapy
  • Demonstrated expertise in LVV and/or RVV systems
  • End-to-end experience from early development through commercialization
  • Strong understanding of:
    • Viral vector development across phases
    • Analytical characterization strategies
    • Manufacturing and tech transfer considerations for viral vector
  • Experience leading cell therapy programs (e.g., CAR-T)
  • Proven ability to lead in a highly matrixed, cross-functional environment
  • Track record of influencing portfolio and strategic decisions for successful drug development

Preferred Qualifications

  • Exposure to in vivo gene delivery platforms
  • Sound knowledge in RVV development and CMC aspects

Leadership Attributes

  • Enterprise mindset - prioritizes product and patient impact over functional optimization
  • Technical depth with judgment - knows when to go deep and when to elevate
  • Clarity and decisiveness - simplifies complexity into actionable direction
  • Talent builder - develops leaders, not just teams
  • Strong influencing skills across matrixed environments
  • Ability to integrate strategy with execution


The salary range for this position is: $255,425.00 - $330,550.00. Kite 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.


Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is based in Santa Monica, CA. For more information on Kite, please visit www.kitepharma.com. Sign up to follow @KitePharma on Twitter at www.twitter.com/kitepharma.

For jobs in the United States:

Kite Pharma 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 contactApplicantAccommodations@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


Kite Pharma 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.


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

For Current Kite Pharma Employees and Contractors:

Please apply via the Internal Career Opportunities portal in Workday.


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