Bristol Myers Squibb
Associate Director, Hypercell, Process Engineer
Bristol Myers Squibb, Harvard, Massachusetts, us, 01451
Associate Director, Hypercell, Process Engineer
Join to apply for the Associate Director, Hypercell, Process Engineer role at Bristol Myers Squibb
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
At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team.
The Hypercell team is driving transformation across Cell Therapy by streamlining supporting processes through digital, automation, and AI-enabled solutions. We are seeking a Senior Level Process Engineer with deep experience in cell therapy or biologics to support process lifecycle management and enable scalable, compliant, and efficient operations. This role will be pivotal in advancing Hypercell’s mission to reduce complexity, eliminate duplication, and improve cost-effectiveness across the network.
Shifts Available Monday - Friday, Standard Working Hours
Responsibilities
Develop tools for automated processing of:
Process Performance Qualification (PPQ) protocols/reports
Continued Process Validation (CPV) reports, Annual Product Quality Reports (APQRs), summarizing process performance and improvement opportunities.
Statistical process monitoring improvements
Collaborate with cross-functional teams including MS&T, QA, Regulatory, and Manufacturing to support tech transfer, validation, and regulatory submissions.
Work closely with Business Insights & Technology (BI&T) colleagues to build data hierarchies and enable automated report writing using available source data.
Support the development and deployment of AI-facing tools that deliver innovative and efficient solutions for end users across the business.
Partner with digital and automation leads to integrate smart technologies into supporting processes.
Mentor junior engineers and contribute to a culture of innovation, technical excellence, and continuous improvement.
Knowledge and Skills
Strong understanding of GMP regulations and regulatory expectations for advanced therapies.
Experience with closed-system processing, aseptic techniques, and single-use technologies.
Proficiency in data analysis tools and statistical software (e.g., JMP, Minitab, Python).
Excellent communication, project management, and problem‑solving skills.
Experience with digital manufacturing platforms, automation technologies, and AI-driven process optimization.
Familiarity with tech transfer across global sites and external partners.
Demonstrated ability to lead cross‑functional teams and drive strategic initiatives.
Basic Requirements
Bachelor's, Master's, or PhD in Chemical Engineering, Biochemical Engineering, Biotechnology, or related field.
7-10 years of experience in cell therapy or biologics manufacturing, with hands‑on expertise in PPQ, deviations, change control, statistical monitoring, and APQRs.
Compensation Overview Devens - MA - US: $179,520 - $217,536 Seattle - WA: $184,550 - $223,634 Summit West - NJ - US: $167,770 - $203,301 Additional incentive cash and stock opportunities (based on eligibility) may be available. Final, individual compensation will be decided based on demonstrated experience.
Equal Employment Opportunity 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.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
BMS strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
Legal Disclaimers Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
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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
At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team.
The Hypercell team is driving transformation across Cell Therapy by streamlining supporting processes through digital, automation, and AI-enabled solutions. We are seeking a Senior Level Process Engineer with deep experience in cell therapy or biologics to support process lifecycle management and enable scalable, compliant, and efficient operations. This role will be pivotal in advancing Hypercell’s mission to reduce complexity, eliminate duplication, and improve cost-effectiveness across the network.
Shifts Available Monday - Friday, Standard Working Hours
Responsibilities
Develop tools for automated processing of:
Process Performance Qualification (PPQ) protocols/reports
Continued Process Validation (CPV) reports, Annual Product Quality Reports (APQRs), summarizing process performance and improvement opportunities.
Statistical process monitoring improvements
Collaborate with cross-functional teams including MS&T, QA, Regulatory, and Manufacturing to support tech transfer, validation, and regulatory submissions.
Work closely with Business Insights & Technology (BI&T) colleagues to build data hierarchies and enable automated report writing using available source data.
Support the development and deployment of AI-facing tools that deliver innovative and efficient solutions for end users across the business.
Partner with digital and automation leads to integrate smart technologies into supporting processes.
Mentor junior engineers and contribute to a culture of innovation, technical excellence, and continuous improvement.
Knowledge and Skills
Strong understanding of GMP regulations and regulatory expectations for advanced therapies.
Experience with closed-system processing, aseptic techniques, and single-use technologies.
Proficiency in data analysis tools and statistical software (e.g., JMP, Minitab, Python).
Excellent communication, project management, and problem‑solving skills.
Experience with digital manufacturing platforms, automation technologies, and AI-driven process optimization.
Familiarity with tech transfer across global sites and external partners.
Demonstrated ability to lead cross‑functional teams and drive strategic initiatives.
Basic Requirements
Bachelor's, Master's, or PhD in Chemical Engineering, Biochemical Engineering, Biotechnology, or related field.
7-10 years of experience in cell therapy or biologics manufacturing, with hands‑on expertise in PPQ, deviations, change control, statistical monitoring, and APQRs.
Compensation Overview Devens - MA - US: $179,520 - $217,536 Seattle - WA: $184,550 - $223,634 Summit West - NJ - US: $167,770 - $203,301 Additional incentive cash and stock opportunities (based on eligibility) may be available. Final, individual compensation will be decided based on demonstrated experience.
Equal Employment Opportunity 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.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
BMS strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
Legal Disclaimers Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
#J-18808-Ljbffr