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Process Automation Engineer Cell Therapy Jobs (NOW HIRING)

Process Automation Engineer Location: North Carolina (Onsite Only) Job Overview: We are hiring a Process Automation Engineer to support commissioning, integration, and startup of automated inspection ...

The Process Automation Engineer continuously supports plant processing, packaging and utility systems for reliability, total cost of ownership, effectiveness tracking, documenting areas of success ...

... cell therapy clinical trials and are proud to be a part of the process that leads to new cures ... The Automation Engineer is responsible for the administration of all facilities and process ...

Process Automation Engineer As a Process Automation Engineer, you will support the Clinton Manufacturing site by delivering and optimizing automation and control systems that drive safe, reliable ...

... cell therapy clinical trials and are proud to be a part of the process that leads to new cures ... The Automation Engineer is responsible for the administration of all facilities and process ...

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Process Automation Engineer Cell Therapy information

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$50.5K

$107.9K

$172.5K

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

As of Jul 19, 2026, the average yearly pay for process automation engineer cell therapy in the United States is $107,918.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,500.00 and $130,500.00 per year, depending on experience, location, and employer.

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 the key skills and qualifications needed to thrive as a Process Automation Engineer in Cell Therapy, and why are they important?

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.

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.
More about Process Automation Engineer Cell Therapy jobs
What cities are hiring for Process Automation Engineer Cell Therapy jobs? Cities with the most Process Automation Engineer Cell Therapy job openings:
What states have the most Process Automation Engineer Cell Therapy jobs? States with the most job openings for Process Automation Engineer Cell Therapy jobs include:
What job categories do people searching Process Automation Engineer Cell Therapy jobs look for? The top searched job categories for Process Automation Engineer Cell Therapy jobs are:
Infographic showing various Process Automation Engineer Cell Therapy job openings in the United States as of July 2026, with employment types broken down into 95% Full Time, 2% Part Time, and 3% Contract. Highlights an 82% Physical, 5% Hybrid, and 13% Remote job distribution, with an average salary of $107,918 per year, or $51.9 per hour.
Robotics Software Engineer - Cell Therapy Automation

Robotics Software Engineer - Cell Therapy Automation

AstraZeneca

Tarzana, CA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 19 days ago


AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 44 frontline employees who took The Breakroom Quiz

18th of 74 rated pharmaceutical


Job description

Do you have a passion for IT, automation, and robotics? Would you like to join a winning team supporting the next generation of Cell Therapy manufacturing in one of the world's leading pharmaceutical companies? If you thrive in an environment of innovation and change in a fast-growing organization, then this could be the role for you.
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.
Introduction to Role
Join us at AstraZeneca, a place that champions knowledge-sharing, ambitious thinking, and innovation. We are looking for an integral member to join our Cell
Therapy Supply Chain - Robotics & Automation IT team. This role has a global remit and will play a critical part in delivering IT infrastructure, software integration, and cybersecurity capabilities for our robotic manufacturing platform.
The role focuses on enabling the deployment and sustained operation of robotic clusters within a GMP cell therapy manufacturing environment. You will be responsible for ensuring seamless IT/OT integration, supporting automation programming, managing vendor software platforms, and ensuring compliance with pharmaceutical cybersecurity standards. This position supports our strategic partnership with an external robotics vendor and directly contributes to patient-impacting manufacturing timelines.
Accountability
In this role, you will be responsible for delivering reliable IT and software engineering support across the full lifecycle of robotic cluster deployment-from Factory Acceptance Testing (FAT) through Site Acceptance Testing (SAT), installation qualification, operational qualification, and ongoing production operations. You will manage integration between robotic systems and enterprise platforms (MES, LIMS, ELN), implement cybersecurity controls aligned with DoD Zero Trust architecture and ISA-62443 standards, and collaborate cross-functionally with supply chain, quality, engineering, and external vendor teams.
You will serve as the primary technical interface between AstraZeneca IT and the robotics vendor's software and automation engineering teams, ensuring that platform readiness milestones are met and that all software licensing, data integrity, and system availability requirements are fulfilled.
Typical responsibilities
  • IT/OT Integration & Architecture: Design and maintain robust OT/IT network segmentation, low-latency connectivity for real-time robotic control, and high-availability infrastructure targeting 99.99% uptime for production-critical automation systems.
  • Cybersecurity & Compliance: Implement and enforce cybersecurity measures including Role-Based Access Control (RBAC), firewall segmentation, endpoint protection, patch management, SIEM integration, and audit logging in alignment with DoD Zero Trust Reference Architecture, ISA-62443, and FDA 21 CFR Part 11.
  • Software & Automation Support: Support automation programming for robotic platforms, resolve software licensing issues, and coordinate with vendor engineering teams on software development lifecycle (SDLC) activities.
  • System Integration: Ensure seamless integration of robotic clusters with Manufacturing Execution Systems (MES) such as PAS-X orTULIP, and with LIMS & ELN platforms to guarantee end-to-end traceability and electronic batch record compliance.
  • Data Management & Traceability: Ensure all data acquisition systems support electronic records and electronic signatures per 21 CFR Part 11, maintain high-fidelity audit trails, and enable capture of process parameters, batch data, and material genealogy.
  • IoT & Environmental Monitoring: Support IoT sensor integration for real-time environmental and equipment monitoring, configure automated alerting and escalation protocols, and maintain alarm management systems.
  • Disaster Recovery & Business Continuity: Develop, test, and maintain disaster recovery plans for cloud-based and on-premise software/data systems; define and meet Recovery Time Objectives (RTO) and Recovery Point Objectives (RPO).
  • Vendor Collaboration & FAT/SAT Support: Serve as the IT point of contact during FAT/SAT execution, support qualification activities, manage deviations and mitigation plans related to IT readiness, and ensure documentation alignment with project milestones.
  • Cloud Platform Management: Support and manage cloud infrastructure associated with the robotic cluster platform (estimated at $2.5M annual cloud fee per cluster), ensuring security, cost efficiency, and performance.

Essential requirements
  • Bachelor's degree in computer science, Software Engineering, Information Technology, or a related field (master's degree preferred).
  • 5+ years experience in IT/OT environments supporting automation, robotics, or advanced manufacturing systems.
  • Strong knowledge of cybersecurity frameworks including Zero Trust architecture, ISA-62443, and NIST standards.
  • Demonstrated experience with MES platforms (e.g., PAS-X or TULIP), LIMS, and ELN systems integration.
  • Proficiency in programming languages such as Python, C++, or C#, and familiarity with robotic frameworks (ROS, UR platforms, or similar).
  • Working knowledge of FDA 21 CFR Part 11, GxP compliance requirements, and pharmaceutical data integrity principles.
  • Experience with cloud platforms (AWS, Azure, or GCP) and IoT integration in manufacturing environments.
  • Strong project management skills, including the ability to manage multiple concurrent workstreams, vendor timelines, and cross-functional dependencies.
  • Excellent communication skills with the ability to translate complex technical topics for non-technical stakeholders.
  • Comfort with risk and ambiguous situations in a rapidly evolving, first-of-its-kind program.

Desirable qualifications
  • Experience working in advanced manufacturing systems and environments.
  • Familiarity with ISPE GAMP 5 validation framework for computerized systems.
  • Experience supporting FAT/SAT and IQ/OQ qualification activities.
  • Knowledge of DevSecOps practices and Scaled Agile Framework (SAFe).
  • Understanding of SEC cybersecurity disclosure requirements (17 CFR Parts 229, 232, 239, 240, 249).

The annual base pay for this position ranges from $122,985.60 - $184,478.40. 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.
When we put unexpected teams in the same room, we ignite ambitious thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility.
Join us in our unique and ambitious world.
Why AstraZeneca:
Here, courage, curiosity, and collaboration fuel a relentless focus on transforming cancer outcomes, powered by a pipeline that fuses innovative science with advanced technology. You will work in an environment where unexpected teams come together to fuel bold ideas, backed by meaningful investment and a clear path from discovery to impact. We value kindness alongside ambition, and we empower leaders at every level to ask sharp questions, take smart risks, and turn data into decisions that help patients sooner.
Date Posted
30-Jun-2026
Closing Date
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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