Engineer II, CAR T Clinical MSAT
Working with UsChallenging.
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.
Position:
Engineer II, CAR T Clinical MSATLocation:
Warren, NJWorking 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 Position SummaryThe Manufacturing Sciences and Technology Engineer Clinical CAR-T Engineering and Technology Support is responsible for supporting the production of personalized cell therapy products for global clinical trials.
Collaborates with SMEs from the Development Group, Global MSAT Group, Supply Chain Group, Manufacturing Group, and Quality Group while providing technical support for the resolution of process deviations, the evaluation and implementation of process changes and continuous improvement support to the production operations to ensure rapid, flawless, compliant, and cost-effective delivery of quality products.
Key ResponsibilitiesEnsure safe and compliant cGMP operations; Maintain permanent inspection readiness and actively support regulatory inspections.
Interface with regulatory authorities as required to support Manufacturing Operations audits.
Foster a culture of compliance and strong environmental, health, and safety performance.
Stay current with industry trends and standards (e.
g.
PDA, ISPE) and participate in best practice forums consistent with function responsibilities.
Provide technical input and investigation support for production related investigations, ensuring compliance with internal standards and regulatory requirements Design and execute test plans and other risk mitigation exercise as part of investigations (e.
g.
Root cause analysis and CAPAs) Sponsor and support the change initiatives and the implementation of process improvement initiatives Support Clinical Production Activities; Support production related investigations, ensuring compliance with internal standards and regulatory requirements.
Continuously monitor, anticipate and permanently resolve issues that may arise during production.
Interface with operators and serve as process SME.
Learn the procedures, analytics and document any known sensitivity.
Provide technical input and investigation support for production related investigations, ensuring compliance with internal standards and regulatory requirements Work closely with Engineering /Maintenance on the design and implementation of new technology and new systems/facilities related to production process needs Review and revise the content of technical documentation (e.
g.
investigations, changes, SOPs and batch records) Interact with other teams including Validation, Development, Operations, QA and Regulatory Display Leadership Qualities; Create an environment of teamwork, open communication, and a sense of urgency Support the change agent in promoting flexibility, creativity, and accountability Support organizational strategic goals and objectives that are linked to the overall company strategy Drive strong collaboration within the plant and across the network Build trust and effective relationships with peers and stakeholders Deliver results through timely and quality decision making and advice Promote a mindset of continuous improvement, problem solving, and prevention Lead project teams, prepare project schedules, coordinate the execution of technical projects and develop presentations to disseminate results to project stakeholders and senior management Qualifications & Experience Experience with the start-up, validation, and licensure of new biopharmaceutical manufacturing facilities Bachelor's Degree required in Engineering or Related Discipline (advanced degree is preferred) 4 or more years of manufacturing support or related experience in the biopharmaceutical industry Basic knowledge of cGMP's and multi-national biopharmaceutical/cell therapy regulations Basic knowledge of facility/clean room design, process, equipment, automation, and validation Intermediate strong verbal/written communication skills and ability to influence at all levels Intermediate ability to think strategically and to translate strategy into actions Intermediate ability to prioritize and provide clear direction to team members in a highly dynamic environment Basic knowledge of quality by design and risk management Basic knowledge of Delta V and OSI Pi Basic experience with Operational Excellence and Lean Manufacturing Work is performed in a typical office environment, with standard office equipment available and used.
Work is generally performed seated but may require standing and walking for up to 10% of the time.
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(TM) , 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 Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.
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 email protected .
Visit careers.
bms.
com/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.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
#LI-OnsiteBMSCARTVETERANIf 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 CareersWith a single vision as inspiring as Transforming patients' lives through science(TM) , 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 ProtocolPhysical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.
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 email protected .
Visit careers.
bms.
com/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.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Recommended Skills Audio Equipments Auditing Automation Biopharmaceuticals Business Process Improvement Clinical Trials Estimated Salary: $20 to $28 per hour based on qualifications.
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.
Position:
Engineer II, CAR T Clinical MSATLocation:
Warren, NJWorking 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 Position SummaryThe Manufacturing Sciences and Technology Engineer Clinical CAR-T Engineering and Technology Support is responsible for supporting the production of personalized cell therapy products for global clinical trials.
Collaborates with SMEs from the Development Group, Global MSAT Group, Supply Chain Group, Manufacturing Group, and Quality Group while providing technical support for the resolution of process deviations, the evaluation and implementation of process changes and continuous improvement support to the production operations to ensure rapid, flawless, compliant, and cost-effective delivery of quality products.
Key ResponsibilitiesEnsure safe and compliant cGMP operations; Maintain permanent inspection readiness and actively support regulatory inspections.
Interface with regulatory authorities as required to support Manufacturing Operations audits.
Foster a culture of compliance and strong environmental, health, and safety performance.
Stay current with industry trends and standards (e.
g.
PDA, ISPE) and participate in best practice forums consistent with function responsibilities.
Provide technical input and investigation support for production related investigations, ensuring compliance with internal standards and regulatory requirements Design and execute test plans and other risk mitigation exercise as part of investigations (e.
g.
Root cause analysis and CAPAs) Sponsor and support the change initiatives and the implementation of process improvement initiatives Support Clinical Production Activities; Support production related investigations, ensuring compliance with internal standards and regulatory requirements.
Continuously monitor, anticipate and permanently resolve issues that may arise during production.
Interface with operators and serve as process SME.
Learn the procedures, analytics and document any known sensitivity.
Provide technical input and investigation support for production related investigations, ensuring compliance with internal standards and regulatory requirements Work closely with Engineering /Maintenance on the design and implementation of new technology and new systems/facilities related to production process needs Review and revise the content of technical documentation (e.
g.
investigations, changes, SOPs and batch records) Interact with other teams including Validation, Development, Operations, QA and Regulatory Display Leadership Qualities; Create an environment of teamwork, open communication, and a sense of urgency Support the change agent in promoting flexibility, creativity, and accountability Support organizational strategic goals and objectives that are linked to the overall company strategy Drive strong collaboration within the plant and across the network Build trust and effective relationships with peers and stakeholders Deliver results through timely and quality decision making and advice Promote a mindset of continuous improvement, problem solving, and prevention Lead project teams, prepare project schedules, coordinate the execution of technical projects and develop presentations to disseminate results to project stakeholders and senior management Qualifications & Experience Experience with the start-up, validation, and licensure of new biopharmaceutical manufacturing facilities Bachelor's Degree required in Engineering or Related Discipline (advanced degree is preferred) 4 or more years of manufacturing support or related experience in the biopharmaceutical industry Basic knowledge of cGMP's and multi-national biopharmaceutical/cell therapy regulations Basic knowledge of facility/clean room design, process, equipment, automation, and validation Intermediate strong verbal/written communication skills and ability to influence at all levels Intermediate ability to think strategically and to translate strategy into actions Intermediate ability to prioritize and provide clear direction to team members in a highly dynamic environment Basic knowledge of quality by design and risk management Basic knowledge of Delta V and OSI Pi Basic experience with Operational Excellence and Lean Manufacturing Work is performed in a typical office environment, with standard office equipment available and used.
Work is generally performed seated but may require standing and walking for up to 10% of the time.
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(TM) , 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 Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.
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 email protected .
Visit careers.
bms.
com/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.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
#LI-OnsiteBMSCARTVETERANIf 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 CareersWith a single vision as inspiring as Transforming patients' lives through science(TM) , 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 ProtocolPhysical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.
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 email protected .
Visit careers.
bms.
com/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.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Recommended Skills Audio Equipments Auditing Automation Biopharmaceuticals Business Process Improvement Clinical Trials Estimated Salary: $20 to $28 per hour based on qualifications.
|
|
 | |
