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Process Automation Engineer Cell Therapy Jobs in Washington

Carlyle

Engineer, AI & Process Automation

Washington, DC · On-site +1

Position Summary The Engineer, AI & Process Automation sits within Carlyle's Corporate Services Technology organization, reporting to the Lead Engineer, AI & Process Automation, and contributes hands ...

Node.Digital

RPA UIPath Developer

Herndon, VA · Hybrid

RPA UIPath Developer (Midlevel) Location: Herndon, VA (Hybrid Work) Required: US Citizenship Requirements The RPA Developer will support the RPA team in the implementation of best practices for RPA ...

Node.Digital LLC

RPA UIPath Developer

Herndon, VA · On-site

$85 - $125/hr

RPA UIPath Developer (Midlevel) Location: Herndon, VA (Hybrid Work) Required: US Citizenship The RPA Developer will support the RPA team in the implementation of best practices for RPA development ...

Node.Digital

RPA UIPath Developer

Herndon, VA · On-site

RPA UIPath Developer (Midlevel) Location: Herndon, VA (Hybrid Work) Required: ship Requirements The RPA Developer will support the RPA team in the implementation of best practices for RPA development ...

Quality Agents

Automation Engineer

Rockville, MD · On-site

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.

kgs

Automation Engineer

Washington, DC · Hybrid

Analyze existing ITSM processes -- including incident management, problem management, change ... Engineer self-service automation capabilities, including virtual agent chatbots, automated ticket ...

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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 Washington?

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

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

Process Automation Engineer Cell Therapy jobs near you

Senior Process Engineer, Global Manufacturing Science and Technology, Cell Therapy Technical Operati

AstraZeneca

Gaithersburg, MD • On-site

$96K - $144K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 15 days ago

AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

22nd of 86 rated pharmaceutical

Job description

AstraZeneca is seeking an experienced senior process engineer for our cell therapy Global Manufacturing Science and Technology (MS&T) team. This position is responsible for supporting the technical oversight of robust, compliant, and cost-effective end-to-end cell therapy manufacturing processes. Activities include leading technology transfer for pivotal clinical manufacturing, process performance monitoring, supporting definition of process validation strategy, leading implementation of continuous process improvements, and contributing to validation and regulatory deliverables to enable commercialization and lifecycle management across a global network of AstraZeneca's manufacturing sites.
The position reports to the Associate Director, Global MS&T, and requires up to 10% domestic and international travel.
Responsibilities
Development and Manufacturing Interface
  • Represent Global MSAT in the technology transfer and process characterization teams to ensure successful commercialization of cell therapy products
  • Communicate Manufacturing Operations needs to the CMC team, and ensure high-quality and timely program deliverables (comparability and validation study completion, etc)
  • Develop PPQ readiness and PPQ execution technical framework for the site MSAT team and oversee execution at the manufacturing sites
  • Implement proactive process analysis and Continued Process Verification (CPV) strategies across manufacturing sites to ensure continued process understanding and process control across all manufacturing sites

Lifecycle Management
  • Provide technical oversight across cell therapy manufacturing lifecycle - from pivotal manufacturing technology transfer, process validation, commercialization, and post-approval
  • Identify and implement process improvements that increase process robustness, cost of goods, plant throughput, and supply continuity
  • Contribute to post-approval process optimization initiatives, comparability strategies, ensuring scientific rigor and managing regulatory risks
  • Proactively identify and mitigate technical and operational risks; ensure standardization across sites and teams

Regulatory & Quality Support
  • Lead global Change Controls and ensure timely implementation and compliance
  • Contribute to authoring CMC sections of regulatory submissions - Pivotal INDa, BLA, MAA, and supplements -with high efficiency and optimal content
  • Partner with quality and regulatory to maintain full compliance with cGMP, ICH guidelines, and global regulatory expectations
  • Develop and defend sound scientific justifications for the integrated control strategy and lifecycle changes

Cross-Functional Partnerships
You will work in close partnership with:
  • Late-Stage Process Development - provide MSAT input for process definition, improvements, and process characterization
  • Site MS&T - partner to ensure timely implementation of process changes and improvements at the sites
  • Quality - ensure process compliance and product quality standards
  • Supply Chain - inform long-range supply planning and risk mitigation

Qualifications
Education
  • B.S or M.S. or Ph.D. in Chemical/Biochemical/Biomedical Engineering, Bioengineering, Biochemistry, Biotechnology, Cell Biology, or a closely related discipline. Advanced degree preferred.

Experience
  • Ph.D. with 1+ years; OR M.S. with 5+ years, OR B.S. with 7+ years of relevant cell therapy/biologics/vaccines industry experience in technical development, MS&T, or CMO management areas.
  • Technical and hands-on expertise in cell therapy manufacturing processes and technologies is highly desirable. Experience in viral vectors, vaccines, or biologics will be considered.
  • Background in GMP manufacturing operations and technology transfer. Experience in process validation and CPV desired.
  • Experience in authoring CMC sections for major regulatory filings (INDa, BLA, MAA) and regulatory inspections.
  • High standards of quality, accountability, and urgency - with the resilience to thrive in a fast-paced cell & gene therapy field.

The annual base pay for this position ranges from $96,196.80 - $144,295.20. 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
09-Aug-2026
Closing Date
27-Aug-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

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