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Cell Therapy Process Development Jobs in Indiana

MEDVACON

Aseptic Process Development - CDMO

IN · On-site

... virology and cell biology Pharmaceutical industry experience in technical support of cGMP ... or process development, including experience with Contract Development and Manufacturing ...

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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 Indiana? For Cell Therapy Process Development jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Cell Therapy Process Development jobs in Indiana look for? The top searched job categories for Cell Therapy Process Development jobs in Indiana are:
Cell Therapy Process Development jobs near you
Infographic showing various Cell Therapy Process Development job openings in Indiana as of August 2026, with employment types broken down into 71% Full Time, and 29% Part Time. Highlights an 100% In-person job distribution.

Cell Therapy Specialist II (26101-B-683-MFG)

Arsenal Biosciences

Francisco, IN • On-site

$84K - $104K/yr

Full-time

Medical, Dental, Vision

Posted 26 days ago

Job description

WHO WE ARE
ArsenalBio, a privately held, clinical-stage programmable cell therapy company engineering advanced CAR T therapies for solid tumors, is seeking a talented Cell Therapy Specialist II to work onsite based in our Hayward/UCSF and San Francisco office.
 
ArsenalBio's mission and purpose is very clear: defeat cancer. With our programmable and computationally driven approach, our team is engineering medicines with the goal to attack cancer's inherent multifaceted nature and overcome the challenges of addressing solid tumors with cell therapy.
 
Driven by a collective of diverse experts across multi-scientific disciplines as well as clinical and manufacturing expertise, we are united in our purpose to develop the optimal medicines for improving patients' lives.
 
This means you'll have the opportunity to work with the best talent in the field of cell therapy, and be part of ONE TEAM advancing therapies for patients who need it most.
 
ArsenalBio is seeking a talented and motivated Cell Therapy Specialist to join the ArsenalBio Technical Operations team supporting cell therapy manufacturing activities. This Specialist will work closely with Manufacturing, Process Development, Quality and other support roles. The position will report into the Director of Manufacturing in supporting day to day manufacturing processes. The individual will also interact cross-functionally across the organization to enable the success of ArsenalBio. This position requires a Tuesday to Saturday schedule  and may require on-call off hours beyond that to support business needs.
 
WHAT YOU'LL DO
  • Perform all tasks associated with the GMP manufacturing of cellular products following batch records, tech transfer protocols, validation protocols and SOPs
  • Assist in set-up, testing, and qualification of manufacturing areas and equipment/fixtures.
  • Work with the Manufacturing team to execute GMP runs in close collaboration with Process Development, MSAT and Quality
  • Demonstrates excellent aseptic/sterile techniques 
  • Prepare and maintain accurate documentation following GMP principles, including following production batch records, SOPs and other documentation
  • Perform equipment and process qualification activities Perform in-process product testing in accordance with standard procedures
 
WHO YOU ARE
  • Bachelor's degree in relevant scientific field. 2+ years of experience in biotechnology/pharmaceutical industry in a manufacturing role
  • Experience in clinical scale cell processing (such as Miltenyi CliniMACS/Prodigy and equivalent platforms) desired
  • Experience in applying techniques learned from prior Cell Therapy experience
  • Excellent written and verbal communication skills
  • Ability to build productive internal/external working relationships
  • Ability to quickly learn new skills and knowledge on the job, demonstrate productivity,
  • and deliver high-quality results
  • Excellent teamwork and collaboration skills
  • Ability to multitask as needed in a start-up environment
 
BENEFITS AND PAY
ArsenalBio has a generous and comprehensive benefits package that includes but is not limited to medical, dental, and vision as well as mental health resources, virtual and telehealth options, coaching, infertility treatment, parental leave and health savings accounts. We also offer flexible work schedules and flexible time off, which includes two extra "Arsenal Days of Rest" every quarter for employees to recharge. 
 
Our people-first culture fosters a deep appreciation for humanity, both in the people we endeavor to serve as well as each other. We are proud to work for a company that is driven by diversity in experiences, ideas and interests, and one that empowers us in an environment that embraces both unity and inclusivity.
 
We have robust tools to help employees take control of their career paths and grow into their best selves. ArsenalBio believes in investing in the well-being of our employees - both at work and at home, as our people are our greatest asset. They bring scientific talents in molecular biology, immunology, pharmacology, protein chemistry, computational biology, automation, genome engineering, software and other fields to make the future happen now.
 
 
We are committed to hiring the best talent from diverse backgrounds. A diverse workforce engenders richness of thought, creativity and discovery. We invite individuals who embrace intellectual achievement to bring their unique personal and professional journeys and together we will build transformative cell therapies for cancer patients.
 
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
 
The estimated base salary offer for the preferred primary location of the San Francisco Bay area ranges from $84,900 - $104,000. Salary ranges for other locations may vary from this range.   Base pay offered may vary depending on job related knowledge, experience, education, and location.  In addition to these factors, we believe in the importance of pay equity and consider internal equity of our current employees as part of any final offer.
 
To all recruitment agencies: ArsenalBio does not accept agency resumes. Please do not forward resumes to our jobs alias, or ArsenalBio employees. ArsenalBio is not responsible for any fees related to unsolicited resumes.
 
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