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Process Engineer III

Kite Pharma -
Santa Monica, CA

Apply Now

Job Details

Full-time
$115,260 - $149,160 a year

Benefits

Health insurance
Dental insurance
Paid time off
Vision insurance
Life insurance

Qualifications

Design of experiments
Pharmaceutical company experience
Bioreactors
Biomedical manufacturing processes
Pharmaceutical manufacturing facility experience

Full Job Description

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

Key responsibilities:

Conduct cell therapy process development experiments using automated platforms.
Design and execute laboratory studies that support the evaluation, development and implementation of new technologies and materials.
Perform hands-on lab-based activities in a cell culture lab, including conception of study designs and analysis of data
Perform process or equipment analysis and trend process or equipment performance.
Develop manufacturing equipment for cell therapy products including hardware, software, and single-use disposable design elements and user-requirements.
Participate in the evaluation of new technologies and materials for introduction into GMP manufacturing
Provide process training to GMP manufacturing personnel.
Support technology transfer and GMP manufacturing operations as needed.
Perform statistical analysis using software such as JMP, Minitab and perform design of experiments (DOEs) as appropriate.
Write and review technical documentation, technical SOPs, draft manufacturing batch records, technical reports and summary reports.
Create and present slides with supporting data to communicate results to stakeholders, cross-functional project teams, senior leadership or external collaborators.
Perform other duties as assigned.

Basic Qualifications:

BS Degree in Biochemical Engineering, Chemical Engineering, Biomedical Engineering, Biotechnology or related discipline with pharmaceutical / biotechnology manufacturing & process development with at least 6 years of experience

MS Degree in Biochemical Engineering, Chemical Engineering, Biomedical Engineering, Biotechnology, or related discipline with pharmaceutical / biotechnology manufacturing & process development with at least 3 years of experience

Preferred Qualifications:

Working experience on cell therapy platforms
Established cell culture lab techniques and aseptic processing in an laboratory such as cell passaging, sampling, fluid handling, media formulation, managing reagents, and cryopreservation.
Practical knowledge of cGMP manufacturing and regulatory regulations and requirements for pharmaceuticals and devices.
Practical demonstration of hands-on process development including use of bioreactors and use of statistical design of experiments is required.
Mastery of scientific and engineering principles related to bioprocessing including scale-up / scale-out approaches, hydrodynamics, mass transfer, and bioreactor design and monitoring fundamentals.
Fundamental understanding of cell biology principles, sub-population types, differentiation, phenotype markers and metabolic pathways.
Knowledge of material science and material compatibility for cell culture applications
Demonstrated knowledge of pharmaceutical manufacturing of biotechnology products, aseptic processing, cell therapy products and process development.
Ability to think critically, troubleshoot, and problem solve in a timely manner.
Excellent interpersonal, verbal and written communication skills are required.
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 and data analysis 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.

The salary range for this position is: $115,260.00 - $149,160.00. 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.

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.

Apply Now

Refine Your Search

implementation engineer iii jobs

Process Engineer III

Level III Software Support Engineer

Engineer III - EDI

Industrial Engineer III

UTILITY WATER/WASTEWATER ENGINEER

Engineer III

Lead Flight Software Engineer

Engineer III (Guidewire)

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IAM Engineer III

Assembly Engineer III

Engineer III, Hogan Applications - McLean, Virginia

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Engineer III or IV - Electric Reliability Compliance

OSP Engineer III

Nuclear Engineer III/IV Instrumentation and Control (I&C) Lead

Cybersecurity Implementation Engineer

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Controls Engineer III

Embedded Quality Assurance Engineer III

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