1

Cell Therapy Process Development Jobs in Missouri

$18.77 - $31.94/hr

... and CAR-T cell therapy for brain tumors. The researcher will perform and optimize complex laboratory procedures including tissue and blood processing, multiparameter flow cytometry ...

$48K - $86K/yr

... and CAR-T cell therapy for brain tumors. The researcher will perform and optimize complex laboratory procedures including tissue and blood processing, multiparameter flow cytometry ...

$16.54 - $22.35/hr

... cell therapy has dramatically improved the long-term survival of relapsed/refractory leukemia ... Questions For frequently asked questions about the application process, please refer to our ...

Reliability Engineer IV

California, MO · On-site

$120K - $160K/yr

Caelux is a pioneering leader in the field of perovskite solar cell technology, committed to ... Process Development to lead and elevate our manufacturing processes. Overview The Reliability ...

... sales process. The Sales Development Representative must identify target accounts in defined ... Second full Year: $121,000 Additional benefits include : * $425 Car Allowance * up to $100 cell ...

Showing results 41-60

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.
Infographic showing various Cell Therapy Process Development job openings in Missouri as of August 2026, with employment types broken down into 70% Full Time, and 30% Part Time. Highlights an 100% In-person job distribution.

Laboratory Supervisor - Vital Tears

Saving-Sight

Kansas City, MO • On-site

Full-time

Re-posted 5 days ago


Job description

Laboratory Operations Supervisor - Biologics Processing
Tuesday-Saturday | 9:00 AM-5:30 PM
Full-Time | Comprehensive benefits
Are you ready to grow your leadership career while staying hands-on in the lab? Join an established, mission-driven, and growing organization committed to investing in its employees, maintaining high-quality operations, and creating long-term career opportunities.
As a Laboratory Operations Supervisor, you'll support daily laboratory operations, develop team members, and help deliver life-changing treatments in a clean room environment. This role offers the opportunity to build management and leadership skills while remaining actively involved in laboratory production and operations.
Why You'll Love This Opportunity
  • Predictable Schedule - Consistent daytime hours that support work-life balance.
  • Supportive Leadership - Leaders who invest in employee development, collaboration, and career growth.
  • Career Growth - Gain valuable supervisory experience while developing the skills needed for future laboratory and operational leadership roles.
  • Meaningful Mission - Help patients suffering from chronic eye conditions regain comfort and improve their daily lives.
  • Hands-On Leadership - Lead and develop a team of 10+ technicians while remaining actively involved in laboratory operations.

What You'll Do
As the ASED Laboratory Supervisor, you'll be a working leader responsible for both daily laboratory operations and team development.
  • Supervise daily laboratory operations and workflow to ensure efficient processing, balanced workloads, and smooth day-to-day operations.
  • Coach, train, and develop laboratory staff through hands-on support, mentoring, and ongoing training.
  • Monitor productivity, quality, and compliance standards while ensuring accurate documentation and adherence to laboratory procedures.
  • Support staffing, scheduling, and inventory management to maintain operational readiness and meet production goals.
  • Drive and support process improvements by identifying opportunities to enhance efficiency, quality, and team performance.

What You'll Bring
  • 1+ years of experience in a laboratory, hospital, specimen processing, blood banking, biologics manufacturing, tissue banking, surgical, or other regulated medical environment.
  • Strong communication, organization, and problem-solving skills
  • Ability to lead in a fast-paced, quality-focused setting
  • Supervisory, lead, training, or team development experience preferred
  • Experience with aseptic technique and clean room practices preferred

Who Thrives in This Role?
This opportunity is ideal for experienced laboratory professionals who enjoy mentoring others, improving processes, and leading by example. Whether you've served as a lead, trainer, mentor, or informal team resource, this role offers the opportunity to take the next step in your leadership career.
You may currently be a:
  • Specimen Processing Lead or Senior Processor
  • Blood Bank Specialist or Lead
  • Clinical Laboratory Technician or Lead
  • Medical Laboratory Scientist
  • Laboratory Operations Specialist
  • Biologics Manufacturing Technician or Lead
  • Tissue Processing Specialist
  • Cell Therapy Manufacturing Technician
  • Sterile Processing Lead
  • Histology or Microbiology Lead

Take the next step from lead/trainer to supervisor while staying hands-on in the lab and making a meaningful impact on patients!
NOTE: The preceding statements describe the nature and level of assignments normally given to job incumbents. They are not an exhaustive list of duties. Additional duties may be assigned. Saving Sight is an Equal Opportunity Employer. We take pride in the diversity of our staff, and seek diversity in our applicants. Saving Sight does not unlawfully discriminate based on any status or condition protected by applicable federal or state law. Saving Sight reserves the right to seek, hire and promote individuals who support the goals and mission of the organization.
At this time, we are only able to consider candidates who do not require current or future sponsorship for employment authorization.