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Process Automation Engineer Cell Therapy Jobs in Maryland

Cell Therapy Specialist I

Frederick, MD · On-site

$60K - $77K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

Cell culture processing experience * Previous experience with cell therapy products is a plus ... The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell ...

Cell Therapy Specialist I

Frederick, MD · On-site

$60K - $77K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

Cell culture processing experience * Previous experience with cell therapy products is a plus ... The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell ...

Senior Automation Engineer

Rockville, MD · On-site

$106K - $139K/yr

Support modifications and improvements to BMS, COPA-DATA Zenon (CDZ), EMS, PLCs, and process automation systems. * Coordinate engineering design, system integration, migration, controls modifications ...

Senior Automation Engineer

Rockville, MD · On-site

$106K - $139K/yr

Support modifications and improvements to BMS, COPA-DATA Zenon (CDZ), EMS, PLCs, and process automation systems. * Coordinate engineering design, system integration, migration, controls modifications ...

Senior Automation Engineer

Rockville, MD

$106K - $139K/yr

Support modifications and improvements to BMS, COPA-DATA Zenon (CDZ), EMS, PLCs, and process automation systems. * Coordinate engineering design, system integration, migration, controls modifications ...

Automation Engineer

Rockville, MD · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The ideal candidate has experience with PLCs, SCADA, building management systems (BMS), and process ... in automation engineering within a biotech, pharmaceutical, or GMP-regulated environment.

Automation Engineer

Rockville, MD · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The ideal candidate has experience with PLCs, SCADA, building management systems (BMS), and process ... in automation engineering within a biotech, pharmaceutical, or GMP-regulated environment.

Automation Engineer

Rockville, MD · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The ideal candidate has experience with PLCs, SCADA, building management systems (BMS), and process ... automation engineering within a biotech, pharmaceutical, or GMP-regulated environment. • ...

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Process Automation Engineer Cell Therapy information

What does a process automation engineer in cell therapy do?

A Process Automation Engineer in Cell Therapy is responsible for designing, implementing, and maintaining automated systems that support the manufacturing of cell-based therapies. They work to optimize processes, improve efficiency, and ensure consistency in the production of therapeutic cells. This role involves collaborating with cross-functional teams, troubleshooting automation equipment, and ensuring compliance with industry regulations. Their work helps bring advanced therapies to patients by streamlining complex manufacturing workflows.

What are the key skills and qualifications needed to thrive as a process automation engineer in cell therapy?

To thrive as a Process Automation Engineer in Cell Therapy, you need a strong background in engineering, biotechnology, or a related field, with experience in process control, automation, and manufacturing operations. Familiarity with automation platforms like PLCs, SCADA systems, DCS, and compliance with GxP regulations is typically required, along with certifications such as Six Sigma or relevant automation credentials. Strong problem-solving, communication, and teamwork skills distinguish top performers in designing and optimizing automated cell therapy processes. These competencies are crucial to ensuring efficient, compliant, and scalable production of advanced therapies in a highly regulated and innovative industry.

How does a process automation engineer in cell therapy typically collaborate with cross-functional teams during project execution?

Process Automation Engineers in Cell Therapy frequently work alongside bioprocess scientists, manufacturing associates, and quality assurance teams to design, implement, and optimize automated systems for cell therapy production. They often participate in multidisciplinary meetings to ensure automation solutions align with regulatory requirements and operational goals. Effective communication and problem-solving skills are crucial, as these engineers must translate technical automation concepts into practical solutions that support the unique needs of biologics manufacturing. This collaborative environment enables them to contribute to process improvements while learning from diverse perspectives within the organization.

What is the difference between Process Automation Engineer Cell Therapy vs Process Validation Engineer?

AspectProcess Automation Engineer Cell TherapyProcess Validation Engineer
CredentialsBachelor's in Engineering, Life Sciences, or related field; experience with automation systemsBachelor's in Engineering, Life Sciences, or related field; experience with validation protocols
Work EnvironmentBiotech manufacturing, cell therapy labs, automation system setupManufacturing facilities, quality assurance labs, validation processes
Industry UsageCell therapy manufacturing companies, biotech firmsPharmaceutical and biotech manufacturing, quality departments

The Process Automation Engineer Cell Therapy focuses on designing, implementing, and maintaining automation systems specific to cell therapy production. In contrast, the Process Validation Engineer ensures manufacturing processes meet quality standards through validation protocols. Both roles require a strong understanding of biotech manufacturing, but their core responsibilities differ in automation versus process validation tasks.

What are popular job titles related to Process Automation Engineer Cell Therapy jobs in Maryland?

For Process Automation Engineer Cell Therapy jobs in Maryland, the most frequently searched job titles are:

What job categories do people searching Process Automation Engineer Cell Therapy jobs in Maryland look for?

The top searched job categories for Process Automation Engineer Cell Therapy jobs in Maryland are:

What cities in Maryland are hiring for Process Automation Engineer Cell Therapy jobs?

Cities in Maryland with the most Process Automation Engineer Cell Therapy job openings:

Infographic showing various Process Automation Engineer Cell Therapy job openings in Maryland as of August 2026, with employment types broken down into 90% Full Time, and 10% Contract. Highlights an 90% In-person, 3% Hybrid, and 7% Remote job distribution.

Cell Therapy Specialist I

Kite Pharma

Frederick, MD • On-site

$60K - $77K/yr

Full-time

Medical, Dental, Vision, Life, PTO

Re-posted 4 days ago


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

We are seeking a highly motivated, Cell Therapy Specialist I to join our newly formed Cell Therapy Manufacturing team at our brand new, state of the art, commercial Cell Therapy facility in Frederick, Maryland.
The Cell Therapy Specialist will perform and/or verify all tasks associated with the manufacture of commercial product following batch records and standard operating procedures (SOPs) to ensure safe and compliant operations as well as works as part of a team to execute GMP runs in close collaboration with Materials Management, Quality Control and Quality Assurance.

Responsibilities include, but are not limited to:

  • Perform all tasks associated with the manufacture of clinical product following batch records and SOPs

  • Work as part of a small team to execute GMP runs in close collaboration with Process Development and Quality

  • Assist in the development of standard operating procedures, batch records, deviations and change controls

  • Successfully troubleshoot processing and equipment issues

  • Other duties as assigned

Basic Qualifications:

  • Associate and 1+ years of biomanufacturing experience OR

  • High School Diploma/GED and 2+ years of biomanufacturing experience


Preferred Qualifications:

  • Bachelor's degree and/or advanced degree or 3 or more years of cGMP experience in a manufacturing pharmaceutical/biotechnology environment

  • Cell culture processing experience

  • Previous experience with cell therapy products is a plus

  • Demonstrated knowledge of pharmaceutical manufacturing of biotechnology products, aseptic processing, cell culture products

  • Strict adherence to SOPs and cGMP regulations, the ability to accurately complete documentation associated with clinical manufacturing

  • Excellent aseptic/sterile techniques and prior experience with cell culture, cell culture equipment including Wave bioreactors

  • Experience with handling and propagation of human primary cells, including T cells

  • Excellent skill in Microsoft word, Excel and data analysis

  • Ability to think critically, and demonstrated troubleshooting and problem solving skills

  • Self-motivated and willing to accept temporary responsibilities outside of initial job description

  • Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment

  • Comfortable in a fast-paced small company environment with minimal direction and able to adjust workload based upon changing priorities

  • Ability to work off-shift and extra hours as required


The salary range for this position is: $60,095.00 - $77,770.00. 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.