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Process Engineer Cell Therapy Jobs in Washington, DC

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Process Engineer Cell Therapy information

See Washington, DC salary details

$56.1K

$104.2K

$161.4K

How much do process engineer cell therapy jobs pay per year?

As of Sep 15, 2026, the average yearly pay for process engineer cell therapy in Washington, DC is $104,219.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,400.00 and $116,700.00 per year, depending on experience, location, and employer.

What does a process engineer in cell therapy do?

A Process Engineer in Cell Therapy is responsible for developing, optimizing, and overseeing the manufacturing processes used to produce cell-based therapies. They ensure that processes are efficient, scalable, and compliant with regulatory standards, while maintaining the quality and safety of the final product. Their work often involves collaborating with scientists, quality teams, and production staff to troubleshoot issues and implement improvements. Process Engineers in this field play a crucial role in bringing innovative cell therapies from the laboratory to clinical and commercial production.

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

To thrive as a Process Engineer in Cell Therapy, you need a strong background in chemical or biomedical engineering, experience with cell culture processes, and often a relevant degree. Familiarity with GMP regulations, bioprocessing equipment, and quality control systems is typically required, along with experience using tools like bioreactors and analytical software. Excellent problem-solving, communication, and project management skills help you collaborate effectively and drive process improvements. These skills ensure the development and optimization of safe, scalable, and compliant cell therapy manufacturing processes.

What are some typical challenges faced by process engineers in cell therapy manufacturing, and how are they addressed?

Process Engineers in Cell Therapy often encounter challenges such as scaling up production from clinical to commercial scale while maintaining stringent quality standards and regulatory compliance. Managing variability in biological materials and ensuring consistency across batches is another common hurdle. These challenges are typically addressed through robust process development, close collaboration with quality and manufacturing teams, and implementation of automation and data-driven process controls. Continuous training and adaptation to evolving regulatory guidelines also play a key role in overcoming these obstacles.

What is the difference between Process Engineer Cell Therapy vs Process Engineer Bioprocess?

AspectProcess Engineer Cell TherapyProcess Engineer Bioprocess
CredentialsBachelor's/Master's in Bioengineering, Chemical Engineering, or related fieldsBachelor's/Master's in Bioengineering, Chemical Engineering, or related fields
Work EnvironmentCell therapy manufacturing facilities, GMP labsBiopharmaceutical production plants, GMP facilities
Industry UsageCell therapy companies, biotech firmsBiotech, pharmaceutical manufacturing
Common Search/ComparisonYesYes

Process Engineer Cell Therapy and Process Engineer Bioprocess roles share similar educational backgrounds and work environments, often within GMP manufacturing settings. The main difference lies in their focus: cell therapy engineers specialize in developing and scaling processes for cellular treatments, while bioprocess engineers work on broader biopharmaceutical production. Both roles are essential in biotech industries and often overlap in skills and certifications.

What are popular job titles related to Process Engineer Cell Therapy jobs in Washington, DC?

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

What job categories do people searching Process Engineer Cell Therapy jobs in Washington, DC look for?

The top searched job categories for Process Engineer Cell Therapy jobs in Washington, DC are:

Infographic showing various Process Engineer Cell Therapy job openings in Washington, DC as of September 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $104,219 per year, or $50.1 per hour.

Lead Automation Engineer - Process

Rockville, MD • On-site

AstraZeneca
Pharmaceutical Product Wholesalers • 10K+ employees

Other

Medical, Dental, Vision, Retirement, PTO

Posted 11 days ago


AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz


Job description

Build the future of cell therapy manufacturing The opportunity – Rockville, MD

Imagine creating the intelligent automation that helps bring advanced cell therapies to patients with greater reliability, speed, and precision. As Senior Automation Engineer – Cell Therapy, you will be a trusted technical leader for high-impact projects and daily manufacturing operations across our Cell Therapy network. You will combine automation, operational technology, robotics, data, and GMP expertise to turn pioneering concepts into dependable manufacturing capability.

Your impact Why this role matters

Based at our Rockville, Maryland site, you will join Facilities and Engineering at a defining moment: the first-of-its-kind implementation of a robotic manufacturing cluster. You will shape the network infrastructure, software and hardware integrations, operating strategy, and lifecycle support that make this platform reliable, compliant, secure, and ready to scale. Lean ways of working and standardized methods will help you simplify complexity, improve performance, and focus effort where it creates the greatest value. Because these capabilities support continuous manufacturing operations, the role participates in a shared 24/7 on-call support model.

What you will do
  • Lead Automation and Operational Technology OT strategy for the site’s first-of-its-kind robotic manufacturing cluster, serving as the primary technical authority and a trusted partner to Manufacturing, Quality, IT, Engineering, and external suppliers.

  • Own and administer critical Automation/OT platforms, including Environmental and Equipment Monitoring Systems, the Process Orchestration Layer, the robotics cluster, and integrated process equipment.

  • Solve complex automation, OT, and robotics challenges, restore performance quickly, and maintain systems in a secure, reliable, and GMP-validated state.

  • Guide equipment lifecycle decisions-from concept, design, and integration through FAT, SAT, commissioning, qualification, validation, maintenance, upgrades, and replacement.

  • Design and continuously improve equipment startup logic, sequences of operation, system architecture, data flows, alarms, notifications, and interfaces for facility and manufacturing assets.

  • Leverage artificial intelligence AI, system and equipment data to identify root causes, anticipate risk, improve reliability, and advance real-time process control.

  • Develop sound capital and operating cost estimates that help leaders prioritize strategic investments.

  • Advance energy-management automation and other continuous-improvement opportunities that strengthen operational and environmental performance.

  • Share expertise, mentor colleagues, and help build enduring automation and robotics capability across the organization.

What you bring – Essential Requirements
  • A bachelor’s degree in engineering or a related technical field, or equivalent practical experience.

  • Five or more years of experience implementing and sustaining process automation or OT systems in manufacturing, laboratory, energy-management, or similarly complex environments.

  • Hands-on experience integrating robotic systems with third-party manufacturing equipment; experience applying artificial intelligence to process execution or real-time control is highly valued.

  • Demonstrated capability across the system lifecycle, including ideation, design, implementation, FAT/SAT, commissioning, qualification, validation, and ongoing support in a GMP-regulated environment.

  • Working knowledge of automation architecture, data flows, configuration, alarm management, remote notifications, and industrial integration standards such as OPC, Modbus, BACnet, Ethernet, hardwired interfaces, and parsers.

  • Experience with relevant platforms and equipment such as Rockwell, Siemens, COPA-DATA Zenon, process orchestration, historians, electronic batch records, or cell therapy manufacturing systems.

  • Familiarity with system integration, data integrity, and zero-trust cybersecurity principles in a regulated environment.

  • A structured, curious approach to troubleshooting and the judgment to balance operational urgency with GMP requirements.

  • Clear communication and collaborative leadership across multidisciplinary teams and stakeholders.

Additional experience that will help you thrive
  • Experience with maintenance-management platforms such as SAP in cell therapy, biotechnology, or pharmaceutical manufacturing.

  • Relevant certifications in process automation, robotics, Rockwell, Siemens, COPA-DATA, industrial networking, cybersecurity, or related disciplines.

Bring your whole perspective

If this opportunity excites you, we encourage you to apply-even if your experience does not align with every preferred qualification. We value people who combine technical depth with curiosity, sound judgment, and a commitment to learning. Join us to build automation that can redefine how cell therapies are manufactured and delivered.

The annual base pay (or hourly rate of compensation) for this position ranges from $108,194.40 – $162,291.60. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.

Date Posted

04-Sep-2026

Closing Date

24-Sep-2026

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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About AstraZeneca

Sourced by ZipRecruiter

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.

Industry

Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Cambridge, Cambridgeshire, GB