Scientist, Package Engineering (Drug Product Development) - Bristol Myers Squibb
New Brunswick, 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 .
This position is part of Sterile Product Development within the Drug Product Development organization located in New Brunswick, NJ. We are looking for a collaborative, self-motivated, and results-driven scientist/engineer with a passion for problem-solving with a focus on packaging development, while also offering versatility in formulation and process development. The successful candidate will thrive in a cross-functional, matrix team environment, contributing to the development of new drug products across pharmaceutics, biologics, and emerging modalities, including but not limited to antibody-drug conjugates, gene therapy, oligonucleotides, and siRNA nanoparticulate delivery, all with the goal of improving patient lives.
Responsibilities:
+ Evaluate and develop new materials, alternate packaging solutions, and packaging systems for sterile dosage forms, based on patient, user, and technical requirements.
+ Generate data and knowledge for regulatory filings by planning and executing experimental plans with minimal supervision, within project timelines.
+ Manage packaging development activities from concept through launch, ensuring adherence to project objectives, timelines, and costs.
+ Conduct process development, optimization, and scale-up studies, ensuring successful technology transfer to clinical manufacturing and commercial sites.
+ Facilitate continuous improvement initiatives to enhance team productivity and foster synergies with stakeholder organizations.
+ Integrate and interpret research data, presenting conclusions at project meetings.
+ Issue periodic reports, ensuring compliance with safety rules, experimental best practices, electronic laboratory notebooks, and other corporate and regulatory guidelines.
+ Stay informed on evolving regulatory and compendia changes, translating pharmaceutical industry trends into business opportunities.
+ Partner with the device development team to ensure system-level requirements for combination products are developed, verified, and validated in accordance with design controls.
+ Develop parenteral dosage forms for clinical and commercial use across various stages of development.
+ Enthusiastically work at the bench to solve challenging pharmaceutical development problems using scientific, engineering, analytical, and numerical analysis techniques.
+ Participate in portfolio and strategy initiative teams to align with business goals.
Qualifications:
+ Ph.D. in Chemical Engineering, Mechanical Engineering, Packaging Science/Engineering Materials Science, or related field with 0-3 years of experience, or MS with 5-7 years of relevant experience.
+ Ability to problem solve using scientific, engineering, analytical, and numerical analysis techniques to support drug product development from early development to product launch as a member of a multidisciplinary project team.
+ Experience in experimental design and execution as well as independent interpretation of data generated via a wide variety of analytical characterization techniques, available from experiments designed by self or others.
+ Curiosity-driven and open-minded approach to solve complex problems and continuously improve processes.
+ Ability to learn new techniques and apply these to address cross-functional development challenges.
+ Excellent interpersonal, communication, and team collaboration skills, with the ability to prioritize tasks, manage projects, and integrate data into decision-making.
#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.
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: R1588177
Updated: 2024-12-17 05:25:16.338 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 .
This position is part of Sterile Product Development within the Drug Product Development organization located in New Brunswick, NJ. We are looking for a collaborative, self-motivated, and results-driven scientist/engineer with a passion for problem-solving with a focus on packaging development, while also offering versatility in formulation and process development. The successful candidate will thrive in a cross-functional, matrix team environment, contributing to the development of new drug products across pharmaceutics, biologics, and emerging modalities, including but not limited to antibody-drug conjugates, gene therapy, oligonucleotides, and siRNA nanoparticulate delivery, all with the goal of improving patient lives.
Responsibilities:
+ Evaluate and develop new materials, alternate packaging solutions, and packaging systems for sterile dosage forms, based on patient, user, and technical requirements.
+ Generate data and knowledge for regulatory filings by planning and executing experimental plans with minimal supervision, within project timelines.
+ Manage packaging development activities from concept through launch, ensuring adherence to project objectives, timelines, and costs.
+ Conduct process development, optimization, and scale-up studies, ensuring successful technology transfer to clinical manufacturing and commercial sites.
+ Facilitate continuous improvement initiatives to enhance team productivity and foster synergies with stakeholder organizations.
+ Integrate and interpret research data, presenting conclusions at project meetings.
+ Issue periodic reports, ensuring compliance with safety rules, experimental best practices, electronic laboratory notebooks, and other corporate and regulatory guidelines.
+ Stay informed on evolving regulatory and compendia changes, translating pharmaceutical industry trends into business opportunities.
+ Partner with the device development team to ensure system-level requirements for combination products are developed, verified, and validated in accordance with design controls.
+ Develop parenteral dosage forms for clinical and commercial use across various stages of development.
+ Enthusiastically work at the bench to solve challenging pharmaceutical development problems using scientific, engineering, analytical, and numerical analysis techniques.
+ Participate in portfolio and strategy initiative teams to align with business goals.
Qualifications:
+ Ph.D. in Chemical Engineering, Mechanical Engineering, Packaging Science/Engineering Materials Science, or related field with 0-3 years of experience, or MS with 5-7 years of relevant experience.
+ Ability to problem solve using scientific, engineering, analytical, and numerical analysis techniques to support drug product development from early development to product launch as a member of a multidisciplinary project team.
+ Experience in experimental design and execution as well as independent interpretation of data generated via a wide variety of analytical characterization techniques, available from experiments designed by self or others.
+ Curiosity-driven and open-minded approach to solve complex problems and continuously improve processes.
+ Ability to learn new techniques and apply these to address cross-functional development challenges.
+ Excellent interpersonal, communication, and team collaboration skills, with the ability to prioritize tasks, manage projects, and integrate data into decision-making.
#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.
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: R1588177
Updated: 2024-12-17 05:25:16.338 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