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Cell Therapy Process Development Jobs in New York

TCWGlobal

Process Equiptment Engineer

Bridgewater, NJ

$40 - $50/hr

These systems are actively running patient products in a GMP cell therapy manufacturing environment. This role is focused on keeping the process running, identifying issues quickly, performing basic ...

TCWGlobal

Process Equiptment Engineer

Bridgewater, NJ

$40 - $60/hr

These systems are actively running patient products in a GMP cell therapy manufacturing environment. This role is focused on keeping the process running, identifying issues quickly, performing basic ...

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Cell Therapy Process Development information

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

To thrive in Cell Therapy Process Development, you need a solid background in cell biology, biotechnology, or a related field, often supported by a relevant degree and experience with cell culture techniques. Familiarity with bioprocessing equipment, Good Manufacturing Practice (GMP) regulations, and analytical tools such as flow cytometry and PCR is typically required. Strong problem-solving skills, attention to detail, and effective teamwork enhance performance in this collaborative and innovative environment. These competencies ensure the safe and efficient development of cell therapies, meeting rigorous quality standards and advancing clinical applications.

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

Professionals in Cell Therapy Process Development often encounter challenges such as scaling up production processes from laboratory to clinical or commercial scale while maintaining product quality and consistency. Additional hurdles include adhering to strict regulatory requirements and managing complex collaborations across cross-functional teams, like quality assurance, regulatory affairs, and manufacturing. These challenges are typically addressed through rigorous process optimization, thorough documentation, and ongoing communication with stakeholders to ensure that all aspects of the process meet industry standards and regulatory expectations.

What is the difference between Cell Therapy Process Development vs Cell Therapy Manufacturing Specialist?

AspectCell Therapy Process DevelopmentCell Therapy Manufacturing Specialist
CredentialsTypically requires a degree in biology, biochemistry, or biomedical engineering; certifications in GMP or cell therapy are commonSimilar credentials; often holds degrees in related fields and GMP certifications
Work EnvironmentResearch labs, development facilities, early-stage process optimizationManufacturing plants, production floors, quality control labs
Industry UsageFocuses on developing and optimizing cell therapy processesInvolved in large-scale production and process execution

Cell Therapy Process Development professionals focus on designing and refining cell therapy procedures, while Cell Therapy Manufacturing Specialists handle the production and quality assurance in manufacturing settings. Both roles require similar educational backgrounds and certifications but differ mainly in their work environment and specific responsibilities.

What is cell therapy process development?

Cell Therapy Process Development refers to the design, optimization, and scaling up of manufacturing processes for cell-based therapies, such as CAR-T cells or stem cell products. Professionals in this field work on translating laboratory research into reproducible, efficient, and safe production methods that meet regulatory standards. This involves working with cell culture techniques, bioreactors, quality control, and process validation to ensure that therapies can be produced consistently for clinical and commercial use. The goal is to develop robust processes that deliver safe and effective cell therapies to patients.
What are popular job titles related to Cell Therapy Process Development jobs in New York? For Cell Therapy Process Development jobs in New York, the most frequently searched job titles are:
What job categories do people searching Cell Therapy Process Development jobs in New York look for? The top searched job categories for Cell Therapy Process Development jobs in New York are:
What cities in New York are hiring for Cell Therapy Process Development jobs? Cities in New York with the most Cell Therapy Process Development job openings:
Cell Therapy Process Development jobs near you
Infographic showing various Cell Therapy Process Development job openings in New York as of August 2026, with employment types broken down into 70% Full Time, and 30% Part Time. Highlights an 100% In-person job distribution.

Process Equiptment Engineer

TCWGlobal

Bridgewater, NJ

$40 - $50/hr

Contractor

Re-posted 3 days ago

Job description

Process Equiptment Engineer

Full Time, Direct Hire

Monday-Friday 7am-4:30pm OR 6pm-6am (5 days on/5 days off)

Bridgewater, NJ

$40-50/hr + Benefits

Please scroll to the bottom of this posting to review an important Candidate Safety & Fraud Awareness Disclaimer from TCWGlobal.


Position Summary

We are seeking Factory Service Engineers to support fully automated gene and cell therapy manufacturing platforms. These systems are actively running patient products in a GMP cell therapy manufacturing environment.

This role is focused on keeping the process running, identifying issues quickly, performing basic equipment troubleshooting, and clearly communicating what is happening on the production floor. The ideal candidate has GMP manufacturing, process support, MSAT, biotech/pharma production, or equipment support experience, plus enough hands-on mechanical ability to troubleshoot basic equipment issues.

What You’ll Do

  • Support gene therapy systems that are already built and processing patient cartridges
  • Monitor equipment and process performance during production runs
  • Identify process or equipment issues and communicate observations clearly to technical teams
  • Perform basic hands-on troubleshooting, including loose cables, sensor adjustments, simple mechanical issues, and equipment alarms
  • Support preventive maintenance, repairs, calibration, and troubleshooting activities
  • Work with manufacturing, quality, engineering, and service teams to resolve production issues
  • Document maintenance, troubleshooting, and support activities in a GMP-compliant manner
  • Support change controls, CAPA investigations, SOPs, and work instructions as needed
  • Participate in training to learn gene and cell therapy manufacturing platforms and process flow
  • Support after-hours/on-call needs as required for GMP operations

What We’re Looking For

  • Bachelor’s degree in engineering, life sciences, or related field, or equivalent technical experience
  • 3+ years of experience in GMP manufacturing, biotech, pharma, cell therapy, or regulated production support
  • Strong process understanding; able to recognize when a process is not running as expected
  • Basic hands-on mechanical aptitude and troubleshooting ability
  • Ability to clearly explain what you are seeing so engineers or technical teams can resolve the issue
  • Experience supporting automated manufacturing equipment, process equipment, or production systems
  • Strong documentation skills and understanding of GMP expectations
  • Comfortable working in a fast-paced manufacturing environment where patient product is involved
  • Able to lift up to 50 lbs and work onsite in Bridgewater, NJ

Strong Backgrounds for This Role

  • Process Technician
  • Manufacturing Technician
  • Manufacturing Associate with strong equipment/process experience
  • MSAT Associate
  • Bioprocess Technician
  • GMP Production Support Technician
  • Equipment Support Engineer
  • Maintenance Technician from pharma, biotech, or medical device
  • Cell therapy or gene therapy manufacturing technician

Nice to Have

  • Cell therapy, gene therapy, or biologics manufacturing experience
  • Experience with automated GMP manufacturing equipment
  • Experience with CMMS systems such as Blue Mountain, Maximo, SAP PM, or eMaint
  • Experience with deviations, CAPAs, change controls, SOPs, and GMP documentation
  • Basic electrical or mechanical troubleshooting experience


TCWGlobal is an equal opportunity employer. We do not discriminate based on age, ethnicity, gender, nationality, religious belief, or sexual orientation.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Important Candidate Safety Notice

This position has been verified and officially approved by TCWGlobal.

Please be aware that fraudulent recruiters and fake job postings may attempt to impersonate legitimate companies online. For your protection:

• Only trust communication from verified TCWGlobal representatives

• Ensure a TCWGlobal recruiter is present on all official phone or video interviews

• TCWGlobal will never request payment, gift cards, cryptocurrency, or sensitive banking information during the hiring process

• Do not share sensitive personal information with unverified individuals or suspicious third parties

• If you are unsure whether a posting or recruiter is legitimate, we encourage you to verify active opportunities directly through https://www.tcwglobal.com/client-jobs or by contacting hello@tcwglobal.com

TCWGlobal is committed to protecting candidates and maintaining a safe, transparent, and professional hiring experience.