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Process Engineer Cell Therapy Jobs in Arizona (NOW HIRING)

Processing Lead

Phoenix, AZ ยท On-site

$102K - $133K/yr

From sample handling to inventory control, your work supports the production of plasma-derived therapies that help patients around the world. What you'll do * Process plasma and samples in accordance ...

As an Automation Engineer , you will design, develop, and support automated manufacturing equipment ... solar cell and module manufacturing processes. * Program, configure, and commission automation ...

Manufacturing Sr Engineer I

Scottsdale, AZ

$91K - $125K/yr

Engineering services may include cell management, process development, project management, process validation, tool design, and trouble shooting. How You'll Create Impact * Creating, maintaining, and ...

Manufacturing Sr Engineer I

Kingman, AZ

$81K - $111K/yr

Engineering services may include cell management, process development, project management, process validation, tool design, and trouble shooting. How You'll Create Impact * Creating, maintaining, and ...

Manufacturing Sr Engineer I

Yuma, AZ

$90K - $123K/yr

Engineering services may include cell management, process development, project management, process validation, tool design, and trouble shooting. How You'll Create Impact * Creating, maintaining, and ...

Manufacturing Sr Engineer I

Phoenix, AZ

$90K - $123K/yr

Engineering services may include cell management, process development, project management, process validation, tool design, and trouble shooting. How You'll Create Impact * Creating, maintaining, and ...

Manufacturing Sr Engineer I

Tucson, AZ

$86K - $117K/yr

Engineering services may include cell management, process development, project management, process validation, tool design, and trouble shooting. How You'll Create Impact * Creating, maintaining, and ...

You will work in direct collaboration with PV Manufacturing process engineers who are focused on ... Develop a strong understanding of end-to-end solar cell and module processes and design features

... processes. The ideal candidate will follow established work instructions and quality standards ... Record data as it relates to productivity, first article inspections, and cell needs * May assist ...

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Process Engineer Cell Therapy information

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, and why are they important?

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 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 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 cities in Arizona are hiring for Process Engineer Cell Therapy jobs? Cities in Arizona with the most Process Engineer Cell Therapy job openings:
Lead Manufacturing Process Engineer(12 Month Contract to Hire)

Lead Manufacturing Process Engineer(12 Month Contract to Hire)

Celestica International LP

Tucson, AZ โ€ข On-site

Other

This job post hasย expired 1 day ago.ย Applications are no longer accepted.


Job description

Req ID: 137330ย 
Remote Position: No
Region: Americasย 
Country: USAย 
State/Province: Arizonaย 
City: ย Tucson Onsite

Summary

1st Shift 12 Month Contract or Contract to hire

The Lead Manufacturing Process Engineer will provide technical leadership and swift resolution for all manufacturing issues pertaining to they cabin pressure controller cell within an aerospace manufacturing environment subject to ITAR (International Traffic in Arms Regulations). The role strongly emphasizes the ability to disposition non conforming hardware, read and interpret detailed mechanical prints, and work cross functionally with program management and quality teams to resolve issues. Practical mechanical experience, strong communication skills, and a collaborative approach are essential.

All duties are performed in compliance with ITAR; U.S. person status (citizen, national, lawful permanent resident, or protected individual as defined by 8 U.S.C. 1324b(a)(3)) is required.ย 

Key Responsibilities
  • Perform design of experiments (DOE) in support of root correction actions (RCCA).ย 
  • Read and interpret mechanical prints and equipment documentation to efficiently identify, diagnose, and resolve faults.
  • Partner with technicians and colleagues to drive troubleshooting efficiency and support operational throughput
  • Communicate clearly and effectively with technicians, supervisors, engineering management, and all relevant stakeholders to resolve production and test issues.
  • Contribute to the development and maintenance of documentation, work instructions, and reports associated with troubleshooting and repair.
  • Adapt to unfamiliar or legacy hardware environments, applying core manufacturing and troubleshooting skills from the outset; product-specific knowledge will be acquired on the job.
  • Maintain current knowledge of industry standards, regulations, and best practices relevant to aerospace, high-reliability, and ITAR-governed manufacturing.
  • Uphold all actions and documentation to ensure compliance with ITAR and related export control requirements.
Required Qualifications
  • Proficient in reading and interpreting mechanical prints and technical documentation
  • Excellent interpersonal and communication skills, with the ability to collaborate and share knowledge across multidisciplinary teams
  • Experience working with outflow control valves and assorted mechanical components.
  • Relevant experience may come from a variety of educational and career paths (e.g., electrical engineering, electronics technology, or equivalent practical background); a degree is not strictly required if capability is proven
  • Experience in aerospace, defense, automotive, medical devices, or other high-reliability electronics manufacturing sectors is welcome but not required
  • Must be a U.S. person as defined by ITAR (citizen, national, lawful permanent resident, or protected individual per 8 U.S.C. 1324b(a)(3)), due to the nature of aerospace manufacturing and regulatory requirements.
Preferred Qualifications
  • Hands-on experience troubleshooting legacy or aging hardware platforms
  • Proven ability to use SAP, JIRA, Teamcenter.
  • Familiarity with configuration control and documentation change managementย 
  • Ability to quickly learn and adapt to unique company-specific tools, production platforms, and regulatory procedures
  • Deep mechanical expertise.
  • Direct experience working with vendors.
Physical Demands
  • Work is conducted in standard office and manufacturing environments.
  • Extended periods may be required at a computer or using test equipment; some standing, sitting, and manual dexterity are needed for assembly and troubleshooting
  • Occasional travel may be necessary.
Additional Information
  • Applicants from all backgrounds are encouraged to apply, provided technical requirements are met.
  • The organization values inclusivity, equal opportunity, and compliance with all legal and regulatory standards, including ITAR
Typical Experience
  • 3-5 years of related experienc;Experience in similar job roles
Typical Education

Bachelor degree or consideration of an equivalent combination of education and experience.

Educational Requirements may vary by Geography

Notes

This job description is not intended to be an exhaustive list of all duties and responsibilities of the position. Employees are held accountable for all duties of the job. Job duties and the % of time identified for any function are subject to change at any time.

Celestica is an equal opportunity employer. All qualified applicants will receive consideration for employment and will not be discriminated against on any protected status (including race, religion, national origin, gender, sexual orientation, age, marital status, veteran or disability status or other characteristics protected by law).
At Celestica we are committed to fostering an inclusive, accessible environment, where all employees and customers feel valued, respected and supported. Special arrangements can be made for candidates who need it throughout the hiring process. Please indicate your needs and we will work with you to meet them.

COMPANY OVERVIEW:
Celestica (NYSE, TSX: CLS) enables the world's best brands. Through our recognized customer-centric approach, we partner with leading companies in Aerospace and Defense, Communications, Enterprise, HealthTech, Industrial, Capital Equipment and Energy to deliver solutions for their most complex challenges. As a leader in design, manufacturing, hardware platform and supply chain solutions, Celestica brings global expertise and insight at every stage of product development - from drawing board to full-scale production and after-market services for products from advanced medical devices, to highly engineered aviation systems, to next-generation hardware platform solutions for the Cloud.ย Headquartered in Toronto, with talented teams spanning 40+ locations in 13 countries across the Americas, Europe and Asia, we imagine, develop and deliver a better future with our customers.

Celestica would like to thank all applicants, however, only qualified applicants will be contacted.
Celestica does not accept unsolicited resumes from recruitment agencies or fee based recruitment services.

This location is a US ITAR facility and these positions will involve the release of export controlled goods either directly to employees or through the employee's movement within the facility. As such, Celestica will require necessary information from all applicants upon an applicant's acceptance of employment to determine if any export control exemptions or licenses must be filed.ย 
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