Gilead Sciences, Inc. Senior Research Associate, Process Design in Santa Monica, California
Kite is continuing to hire for all open roles. Our interview process may be conducted virtually and some roles will be asked to temporarily work from home. Over the coming weeks and months, we will be implementing a phased approach to bringing employees back to site to ensure the health and safety of our teams.
For Current Kite Pharma Employees and Contractors:
Please log onto your Internal Career Site (https://www.myworkday.com/gilead/d/inst/13102!CK5mGhEKBggDEMenAhIHCgUI1A0QcQ/cacheable-task/2997$2151.htmld) to apply for this job
Kite is seeking a highly motivated individual with cell culture experience to work on innovative T cell therapy for cancer treatment. As a Senior Research Associate in Process Design, you will provide process development support for New INDs, technology transfers, process validations and GMP manufacturing for Kite’s engineered autologous T cell therapy products. Additionally, you will draft and review protocols, production procedures, and process development reports. You will work with the Process Development team to design and scale-out cell therapy processes, manage equipment qualification and support process validation, as well as draft documentation for regulatory filings to advance Kite’s product portfolio.
Hands on execute and collaborate on process design laboratory studies to support process development, optimization and characterization and essential process improvements.
Perform hands on work in a cell culture lab and process training for GMP clinical production.
Participate and influence a cross-functional development team to advance CMC activities
Perform process analysis and trend process performance
Develop manufacturing processes for cell therapy products
Design and execute process development studies to develop a thorough understanding of operating and performance parameters
Perform statistical analysis including design of experiments (DOEs) as appropriate
Write and review technical documentation from writing technical SOPs, draft manufacturing batch records, technical reports and summary reports.
Create slides and supporting data to communicate results to senior leadership.
Other duties as assigned
MA/MS Degree in Biochemical Engineering, Chemical Engineering, or related discipline
BA/BS Degree in Biochemical Engineering, Chemical Engineering, or related discipline with 2+ years of pharmaceutical manufacturing, technology transfer & process development experience
HS Diploma with 5+ years of pharmaceutical manufacturing, technology transfer & process development experience
Demonstrated cell culture and aseptic processing experience including basic cell culture lab techniques such as cell passaging, cryopreservation, formulation of media, aseptic technique using a BSC, cell counting, and managing reagents.
Practical knowledge of cGMP manufacturing and regulatory regulations and requirements for pharmaceuticals and devices.
Practical demonstration of hands on process development including use of statistical design of experiments is required. Experience with bioreactors is desired.
Mastery of scientific and engineering principles
Pharmaceutical products GMP manufacturing experience strongly preferred
Previous experience with cell therapy products is a plus
Understands and employs principles and concepts of Lean Six Sigma or design of experiments to improve process capability is a plus
Experience in statistical analysis using JMP or Minitab
Proven track record of working within cross functional teams
Knowledge of data management tools and statistical process controls
Ability to think critically, and demonstrated troubleshooting and problem solving skills
Excellent interpersonal, verbal and written communication skills
Ability to function efficiently and independently in a changing environment
Self-motivated, strong sense of responsibility, and willing to accept temporary responsibilities outside of initial job description
Well-developed computer skills
High energy level and a positive outlook coupled with the requisite “can do” attitude and a willingness to do what it takes to achieve personal and organizational goals and overcome obstacles
Comfortable in a fast-paced environment with minimal direction and able to adjust workload based upon changing priorities
Ability to work and collaborate in cross functional teams, research, development, manufacturing in a fast pace, dynamic team setting
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 .
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For Current Kite Pharma Employees and Contractors:
Please log onto your Internal Career Site (https://www.myworkday.com/gilead/d/inst/13102!CK5mGhEKBggDEMenAhIHCgUI1A0QcQ/cacheable-task/2997$2151.htmld) to apply for this job.
Change The World With Us
Everyone at Kite is grounded by one common goal – curing cancer. Every day, we aim to establish a direct line between that purpose and our day-to-day work.
We are creating Kite together, with the recognition that the best teams are built by the best people. We maintain an attitude of curiosity, and creativity with each challenge as we develop a new market for cancer therapies. We appreciate and respect one another, and most importantly, we don’t take success for granted.
While we’ve come a long way to make what others viewed as impossible, possible, we know one thing is certain. Today is just the beginning.