Gilead Sciences Inc

Scientist, Process Development (In-Vivo Upstream)

Gilead Sciences Inc$133K — $172K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • B.S., M.S., or PhD/PharmD in science or engineering
  • 6+ years relevant experience with BS, or 4+ years with MS, or none with PhD/PharmD
  • Strong proficiency in mammalian cell culture methods
  • Good understanding of bioprocess scale-up principles
  • Familiarity with cGMP principles
  • Proficient in Microsoft Office and data analysis software like JMP
  • Excellent communication and organizational skills

Responsibilities

  • Design and optimize scalable cell culture processes for Lentivirus manufacturing
  • Develop technical solutions for complex scientific problems
  • Support and optimize manufacturing processes at scale
  • Manage laboratory operations and ensure proper documentation
  • Maintain detailed lab records and follow safety guidelines
  • Apply statistical methods for experimental design and data analysis
  • Train and mentor team members on technical skills and processes

Benefits

  • Company-sponsored medical, dental, vision, and life insurance plans
  • Discretionary annual bonus eligibility
  • Discretionary stock-based long-term incentives
  • Paid time off
  • Access to additional benefits as detailed in company policies
Full Job Description
Job Description

The Scientist, Process Development (In-Vivo Upstream) role designs and executes cell culture/upstream experiments to support development of manufacturing processes for Lentivirus.

This role applies advanced chemistry, biochemistry, and/or engineering principles to deliver robust, scalable processes, supports manufacturing activities and process optimization at scale, and operates with broad autonomy and limited oversight. The Scientist is accountable for end-to-end process performance, scientific soundness, and technical leadership while training and mentoring colleagues.

Key Responsibilities
  • Design and optimize scalable, safe, and cost-effective cell culture/upstream process for Lentivirus manufacturing.
  • Develops technical solutions to complex problems requiring ingenuity and creativity, applying advanced scientific/engineering principles to ensure scientific soundness and performance.
  • Supports manufacturing activities and process optimization at scale, contributing technical expertise to improve process performance and scalability.
  • Manages day-to-day laboratory operations, including planning work, maintaining efficient lab execution, and ensuring effective documentation practices.
  • Keep accurate, detailed laboratory records and comply to all required training and safety guidelines.
  • Apply statistical methodologies and basic modelling approaches to design experiments, perform data analysis, and interpret data.
  • Trains, guides, and mentors colleagues by sharing technical skills, coaching on process execution, and troubleshooting, and strengthening team capability.
  • Communicates technical outcomes in technical reports and presentations
  • Interface with multidisciplinary groups to solve complex issues and promote collaboration.
  • Works independently with broad autonomy and limited oversight; determines approaches for moderately complex assignments under minimal direction.


Education and Experience
  • B.S., M.S, PhD/PharmD in science or engineering
  • BS with 6+ years post-graduate relevant experience in bioprocess/biotechnology, or
  • MS with 4+ years post-graduate relevant experience in bioprocess/biotechnology, or
  • PhD/PharmD with 0 years of experience


Required Qualifications
  • Must have strong scientific understanding and demonstrated hands-on proficiency of cell culturing methods of mammalian cells in flasks and bioreactors
  • Must have demonstrated hands-on proficiency
  • Sound understanding of bioprocess scale-up principles
  • Working knowledge of cGMP principles
  • Proficiency in Microsoft Word, Excel, Power Point, and data analysis software such as JMP, GraphPad
  • Proven ability to collaborate in a dynamic team environment
  • Excellent interpersonal, verbal, and written communication skills
  • Strong organization and problem-solving skills with excellent attention to details


Preferred Experience and Skills
  • Prior experience with process development of viral vectors
  • Prior experience with the use of Design of Experiments (DOE) to support process development experiments.
  • Prior experience with downstream and analytics of large biomolecules
  • Hands-on experience with large scale bioprocessing in either non-GMP or GMP setting
  • Demonstrated mentorship and team leadership


The salary range for this position is: $133,195.00 - $172,370.00. 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 [redacted] on Twitter at www.twitter.com/kitepharma.

For Current Kite Pharma Employees and Contractors:

Please apply via the Internal Career Opportunities portal in Workday.

About Gilead Sciences Inc

Gilead Sciences is a research-based biopharmaceutical company that discovers, develops, and commercializes innovative medicines in areas of unmet need. With each new discovery and experimental drug candidate, they seek to improve the care of patients suffering from life-threatening diseases. Gilead's primary areas of focus include HIV/AIDS, liver disease, and serious cardiovascular and respiratory conditions.

Gilead Sciences Inc Careers

Join the vibrant team at Gilead Sciences Inc, a leader in the biopharmaceutical industry known for its innovative approach to healthcare. At Gilead, we are committed to advancing the care of patients around the globe through rigorous science and research.

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Start your career with Gilead through our internship programs, which offer hands-on experience in biopharmaceutical development and business operations. For seasoned professionals, our employment opportunities span across various disciplines, inviting you to bring your valuable skills to our team.

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Gilead Sciences Inc is not only a great place to work but also offers competitive benefits designed to support the health, well-being, and financial security of our employees and their families. From health insurance to retirement plans and wellness programs, we ensure our team members are taken care of.

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We emphasize the importance of networking and professional development within the company. Regular workshops, seminars, and training sessions are held to enhance your skills and knowledge. Additionally, Gilead’s strong emphasis on internal networking allows for cross-departmental collaboration and innovation.

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Learn more about Gilead Sciences Inc
Size
14,400 employees
Market Cap
$107.2 billion
Industry
Net Income
$123 million
Founded
1987
5 Year Trend
-2.1%
Revenue
$24.6 billion
NASDAQ

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