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Process Engineer Cell Therapy Jobs (NOW HIRING)

Senior Process Engineer

Seattle, WA · On-site

$120K - $135K/yr

The ideal candidate will exhibit an understanding of both cell therapy and viral vector processes ... Build and develop process engineering toolset and best practices for data analysis and ...

The ideal candidate will exhibit an understanding of both cell therapy and viral vector processes ... Build and develop process engineering toolset and best practices for data analysis and ...

Principal Process Engineer

Berkeley, CA · On-site +1

$128K - $192K/yr

Principal Process Engineer As a Principal Process Engineer, you are accountable for the definition ... You support multiple biologics modalities, including rFVIII, mAbs, Cell Therapy, Gene Therapy, and ...

Principal Process Engineer

Berkeley, CA · On-site +1

$128K - $192K/yr

Principal Process Engineer As a Principal Process Engineer, you are accountable for the definition ... You support multiple biologics modalities, including rFVIII, mAbs, Cell Therapy, Gene Therapy, and ...

... cell therapy products and process development * Ability to think critically, and demonstrated ... DPS Engineering Inc. is an Equal Opportunity Employer and employment selection decisions are based ...

Conduct cell therapy process development experiments using automated platforms. * Design and ... MS Degree in Biochemical Engineering, Chemical Engineering, Biomedical Engineering, Biotechnology ...

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Process Engineer Cell Therapy information

See salary details

$49.5K

$92K

$142.5K

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

As of Jun 12, 2026, the average yearly pay for process engineer cell therapy in the United States is $92,018.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $103,000.00 per year, depending on experience, location, and employer.

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.
More about Process Engineer Cell Therapy jobs
What cities are hiring for Process Engineer Cell Therapy jobs? Cities with the most Process Engineer Cell Therapy job openings:
What states have the most Process Engineer Cell Therapy jobs? States with the most job openings for Process Engineer Cell Therapy jobs include:
Infographic showing various Process Engineer Cell Therapy job openings in the United States as of June 2026, with employment types broken down into 100% Contract. Highlights an 100% In-person job distribution, with an average salary of $92,018 per year, or $44.2 per hour.
Senior Scientist, Cell Therapy TRC In Vivo Pharmacology

Senior Scientist, Cell Therapy TRC In Vivo Pharmacology

Bristol-Myers Squibb Company

Seattle, WA • On-site

$104K - $142K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 15 days ago


Bristol Myers Squibb rating

8.0

Company rating: 8.0 out of 10

Based on 48 frontline employees who took The Breakroom Quiz

36th of 71 rated pharmaceutical


Job description

Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.
The Cell Therapy Thematic Research Center is one of BMS's differentiated research platforms delivering innovative therapies to patients. Our mission is to drive leadership in the use of cellular therapies to harness the power of the immune system in treating hematologic malignancies, solid cancers, and autoimmune disease. More specifically, our discovery and translational scientists are focused on developing next-generation, engineered cell-based therapies. The team is committed to discovering and developing transformative therapies that harness the power of the immune system to improve patient outcomes."
Position Summary
The In Vivo Pharmacology team in the Cell Therapy Thematic Research Center has an opening for a highly collaborative and creative Sr. Scientist with a dedication to discovery and development of novel engineered immune effector cell therapeutics for the treatment of cancer and other chronic diseases. The successful candidate will have a strong scientific track-record demonstrating their expertise in immuno-oncology, particularly related to tumor and immune response models in mice, and a desire to lead functional workstreams from early stages/target concept through to IND filing. The role will encompass the direct supervision and mentorship of research associates and contribute to scientific and strategic leadership for the pharmacology function in the context of collaborative, cross-functional BMS R&D project teams. This position is ideal for a motivated and interactive scientist who is passionate about cell therapy and has a proven track record working across highly matrixed teams to drive key decisions for drug discovery and development.
Position Responsibilities
In the role as a Senior Scientist within the In Vivo Pharmacology Team, the ideal candidate will:
  • Lead functional workstreams on highly matrixed cell therapy research project teams from target concept to IND
  • Represent the in vivo pharmacology function on cross-functional research teams, effectively influencing scientific decisions, building alignment, and communicating clear scientific recommendations.
  • Independently design, execute, and interpret complex in vivo pharmacology studies supporting engineered immune cell therapy programs, ensuring next logical steps based on experimental results.
  • Independently author high-quality scientific documents, including presentations, study reports, protocols, and publications; contribute to regulatory and IP filings.
  • Present complex concepts to a range of audiences including governance and departmental meetings
  • Integrate literature, emerging technologies, and evolving immunotherapy modalities to enhance study design and support the development of novel engineered immune cell therapeutics.
  • Supervise and mentor colleagues through functional guidance, scientific feedback, and day-to-day technical support, fostering strong technical execution and scientific rigor.
  • Excel in a fast-paced team environment, meet deadlines, and prioritize work on multiple projects while fostering open and productive scientific communication and collaboration

Experience =
Basic Qualifications:
  • Bachelor's Degree
    • 7+ years of academic and / or industry experience

Or
  • Master's Degree
    • 5+ years of academic and / or industry experience

Or
  • Ph.D. or equivalent advanced degree in the Life Sciences
    • 2+ years of academic and / or industry experience

Preferred Qualifications:
  • Ph.D. in Immunology, Cancer Biology, Virology or a related field with demonstrated expertise in in vivo immuno-oncology models and immune effector cell biology
  • 4+ years of post-degree experience in industry settings focused on immune-based therapies, in vivo immunology, or engineered cell therapies
  • Advanced proficiency in murine tumor model development-including syngeneic, xenograft, and/or T-cell driven models-with a track record of designing and executing studies that inform mechanistic understanding and therapeutic advancement including: cell-based therapies, immunotherapies, and drug combination studies
  • Familiarity with gene editing technologies and delivery methods (e.g., adeno-associated viral vectors, non-viral delivery, CRISPR gene editing)
  • Proven capability to influence project direction through clear communication, scientific leadership, and representation of the in vivo pharmacology function in cross-functional settings.
  • Strong record of scientific authorship, including internal reports, external publications, and contributions to patents or regulatory documentation.

#LI-Onsite
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Compensation Overview:
Seattle - WA: $136,030 - $164,841
The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
  • Health Coverage: Medical, pharmacy, dental, and vision care.
  • Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
  • Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.

Work-life benefits include:
Paid Time Off
  • US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
  • Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays

Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.
*Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as "Transforming patients' lives through science™ ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
On-site Protocol
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
Supporting People with Disabilities
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
Candidate Rights
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
Data Protection
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.
R1599506 : Senior Scientist, Cell Therapy TRC In Vivo Pharmacology

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About Bristol-Myers Squibb

Sourced by ZipRecruiter

Bristol-Myers Squibb is a world-renowned global Biopharmaceutical company headquartered in New York, NY, US. Established in 1887, the company has more than 130 years’ worth of history dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. The company operates in the healthcare industry and thrives on providing a range of pharmaceutical products and services for various medical fields, like oncology, cardiovascular diseases, and immunoscience. Notably, Bristol-Myers Squibb is known for its commitment to relentless research and innovative drug development, which has led to breakthroughs like Opdivo, one of the first immunotherapies.

Industry

Scientific research and development services and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

New York, NY, US