Scientist, Process Analytical Technologies - Bristol Myers Squibb
Summit, NJ
About the Job
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 rich in diversity. 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 .
Our Drug Product Development team is committed to CMC design, development, and commercialization of innovative drug products to improve patient lives. We leverage the best people, collaboration, and cutting-edge innovation to achieve this commitment. BMS's internal engine of innovation includes unrivaled industry leading expertise in CMC development of small molecules, protein biotherapeutics, protein degraders, and other therapeutic modalities. We collaborate closely with our colleagues in R&D and Commercial to design our drug products. Here, you'll get the chance to grow and thrive through opportunities that are uncommon in scale and scope.
Location: New Brunswick / Summit, NJ
Department: Drug Product Development
Job Summary: The PAT Scientist will be responsible for developing and implementing Process Analytical Technology (PAT) strategies and methods to support the development, optimization, and control of drug product manufacturing processes. This role involves working closely with cross-functional teams, including formulation development, manufacturing, analytical, data scientists, predictive modeling and quality assurance, to ensure the successful integration of PAT tools and methodologies.
Key Responsibilities:
+ Develop and implement PAT strategies and methods to monitor and control manufacturing processes.
+ Design and execute experiments to evaluate PAT tools and develop and validate methods.
+ Collaborate as part of multi-disciplinary teams that comprises of formulation scientists, analytical chemists, process engineers, and process modelers to integrate PAT into development of drug product formulations and manufacturing processes.
+ Analyze data from PAT tools to provide insights into process performance and product quality.
+ Develop and maintain documentation related to PAT activities, including protocols, reports, and standard operating procedures (SOPs).
+ Provide technical support and training (via tech transfer activities) to manufacturing teams on the use of PAT tools and methodologies.
+ Stay current with advancements in PAT technologies and regulatory requirements.
+ Participate in regulatory submissions related to PAT.
+ Troubleshoot and resolve issues related to PAT tools and methodologies.
Qualifications / Requirements:
+ Ph.D. (preferred) or M.S. in Analytical Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related field.
+ Recent PhD graduate with 0-2 years of experience or Masters graduate with 2-4 years of industrial experience in the pharmaceutical or biotechnology industry, with a focus on PAT.
+ Strong knowledge of PAT tools such as spectroscopy (NIR, Raman, etc.) and chemometrics.
+ Experience with process development, scale-up, and manufacturing in a GMP environment is preferred.
+ Excellent critical thinking skills and the ability to work independently and as part of a team.
+ Effective communication and people skills.
+ Proficiency in data analysis software and tools.
Working Conditions:
+ Laboratory and manufacturing environment.
+ May require occasional travel to other sites or conferences.
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.
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 an inclusive culture, promoting diversity 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 a diverse 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.
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/ (https://careers.bms.com/eeo-accessibility) eeo-accessibility to access our complete Equal Employment Opportunity statement.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
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/
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Company: Bristol-Myers Squibb
Req Number: R1586230
Updated: 2024-10-11 03:10:46.575 UTC
Location: New Brunswick-NJ
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
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 rich in diversity. 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 .
Our Drug Product Development team is committed to CMC design, development, and commercialization of innovative drug products to improve patient lives. We leverage the best people, collaboration, and cutting-edge innovation to achieve this commitment. BMS's internal engine of innovation includes unrivaled industry leading expertise in CMC development of small molecules, protein biotherapeutics, protein degraders, and other therapeutic modalities. We collaborate closely with our colleagues in R&D and Commercial to design our drug products. Here, you'll get the chance to grow and thrive through opportunities that are uncommon in scale and scope.
Location: New Brunswick / Summit, NJ
Department: Drug Product Development
Job Summary: The PAT Scientist will be responsible for developing and implementing Process Analytical Technology (PAT) strategies and methods to support the development, optimization, and control of drug product manufacturing processes. This role involves working closely with cross-functional teams, including formulation development, manufacturing, analytical, data scientists, predictive modeling and quality assurance, to ensure the successful integration of PAT tools and methodologies.
Key Responsibilities:
+ Develop and implement PAT strategies and methods to monitor and control manufacturing processes.
+ Design and execute experiments to evaluate PAT tools and develop and validate methods.
+ Collaborate as part of multi-disciplinary teams that comprises of formulation scientists, analytical chemists, process engineers, and process modelers to integrate PAT into development of drug product formulations and manufacturing processes.
+ Analyze data from PAT tools to provide insights into process performance and product quality.
+ Develop and maintain documentation related to PAT activities, including protocols, reports, and standard operating procedures (SOPs).
+ Provide technical support and training (via tech transfer activities) to manufacturing teams on the use of PAT tools and methodologies.
+ Stay current with advancements in PAT technologies and regulatory requirements.
+ Participate in regulatory submissions related to PAT.
+ Troubleshoot and resolve issues related to PAT tools and methodologies.
Qualifications / Requirements:
+ Ph.D. (preferred) or M.S. in Analytical Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related field.
+ Recent PhD graduate with 0-2 years of experience or Masters graduate with 2-4 years of industrial experience in the pharmaceutical or biotechnology industry, with a focus on PAT.
+ Strong knowledge of PAT tools such as spectroscopy (NIR, Raman, etc.) and chemometrics.
+ Experience with process development, scale-up, and manufacturing in a GMP environment is preferred.
+ Excellent critical thinking skills and the ability to work independently and as part of a team.
+ Effective communication and people skills.
+ Proficiency in data analysis software and tools.
Working Conditions:
+ Laboratory and manufacturing environment.
+ May require occasional travel to other sites or conferences.
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.
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 an inclusive culture, promoting diversity 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 a diverse 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.
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/ (https://careers.bms.com/eeo-accessibility) eeo-accessibility to access our complete Equal Employment Opportunity statement.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
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/
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Company: Bristol-Myers Squibb
Req Number: R1586230
Updated: 2024-10-11 03:10:46.575 UTC
Location: New Brunswick-NJ
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
Source : Bristol Myers Squibb