Bristol Myers Squibb
Associate Director, Hypercell, Process Engineer
Bristol Myers Squibb, Summit, New Jersey, us, 07902
Overview
Associate Director, Hypercell, Process Engineer Join to apply for the
Associate Director, Hypercell, Process Engineer
role at
Bristol Myers Squibb 3 days ago Be among the first 25 applicants 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 & Benefits
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 then in effect and may include the following Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year\'s holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program. Equal Opportunity
BMS is committed to equal employment opportunity and compliance with applicable laws. Details in the final lines of the original description are kept for legal completeness and may include information about accommodation requests and privacy notices.
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Associate Director, Hypercell, Process Engineer Join to apply for the
Associate Director, Hypercell, Process Engineer
role at
Bristol Myers Squibb 3 days ago Be among the first 25 applicants 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 & Benefits
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 then in effect and may include the following Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year\'s holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program. Equal Opportunity
BMS is committed to equal employment opportunity and compliance with applicable laws. Details in the final lines of the original description are kept for legal completeness and may include information about accommodation requests and privacy notices.
#J-18808-Ljbffr