Associate Specialist, Value Stream Cryo Operations - 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 .
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.
Specialist, Value Steam Cryo Operations is responsible for the Cryopreservation, movement, storage, control of manufacturing patient materials, and support of Liquid Nitrogen storage tanks and equipment at the CAR T manufacturing facility in Summit, NJ. This includes but is not limited to, cryopreservation, storage, inventory control, chain of custody, and material tracking.
Shift Available:
+ Wednesday - Saturday (Alternating Wednesday), Onsite Evening Shift, 2 p.m. - 2:30 a.m.
Responsibilities:
Responsible for cryopreservation and management of including:
+ Handling patient material throughout the material Cryopreservation, storage, distribution, transfer, and disposal.
+ Maintaining sample tracking and chain of custody records in accordance with GMP requirements and written procedures.
+ Ensuring that obsolete or expired samples and materials are destroyed and disposed of according to written procedures.
+ Performing sample queries and periodic storage reports, as required.
+ Assisting management with investigations and deviations related to sample management.
+ Collaborating with other departments to identity and implement process efficiencies.
+ Maintaining metrics for the Value Stream Cryo Operations group.
+ Facilitating cold chain transfers of material, as required.
+ Performs tasks for Cell Therapy products to support product Value Stream outputs according to Current Good Manufacturing Practices (cGMP's) following the current, approved Standard Operating Procedures (SOPs) and Work Instructions (WIs).
+ Maintains timing according to the production schedule to ensure on-time.
+ Cryopreservation support.
+ Cryopreserve Patient material daily, store and manage Inventory of material in LN2 storage locations.
+ Supports manual and electronic batch record executions, deviation investigations, and closure of CAPAs.
+ Maintains timing according to the production schedule to ensure on-time logistics.
+ Ensures all documentation is correct and addresses procedural/documentation errors expeditiously and effectively.
+ Work with management to ensure adequately trained personnel are available to perform all Value Stream Cryo Operations activities.
+ Records patient material handling data and information in a clear, concise, format according to proper GDPs.
+ Able to problem solve with minimal supervision.
+ Works in a team based, cross-functional environment to complete tasks required by shift schedule.
+ Available to work OT when business requires.
+ Willing to work staggered day shift hours.
Knowledge & Skills:
+ Experience with cold chain sample storage and transfer.
+ Knowledge of cGMP/FDA regulated industry.
+ Basic mathematical skills.
+ General understanding of cGMPs.
+ Technical writing capability.
+ Proficient in MS Office applications.
+ Inventory control and/or management.
+ Background to include an understanding of biology, chemistry, medical or clinical practices is a plus.
Basic Requirements:
+ Bachelor's degree
+ OR Associate/ Medical Technical degree and 0-2 years of Manufacturing or Operations experience.
+ OR High School diploma/GED and 2-4 years of Manufacturing experiences.
BMSCART, #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: R1586312
Updated: 2024-10-16 03:41:50.946 UTC
Location: Summit West-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 .
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.
Specialist, Value Steam Cryo Operations is responsible for the Cryopreservation, movement, storage, control of manufacturing patient materials, and support of Liquid Nitrogen storage tanks and equipment at the CAR T manufacturing facility in Summit, NJ. This includes but is not limited to, cryopreservation, storage, inventory control, chain of custody, and material tracking.
Shift Available:
+ Wednesday - Saturday (Alternating Wednesday), Onsite Evening Shift, 2 p.m. - 2:30 a.m.
Responsibilities:
Responsible for cryopreservation and management of including:
+ Handling patient material throughout the material Cryopreservation, storage, distribution, transfer, and disposal.
+ Maintaining sample tracking and chain of custody records in accordance with GMP requirements and written procedures.
+ Ensuring that obsolete or expired samples and materials are destroyed and disposed of according to written procedures.
+ Performing sample queries and periodic storage reports, as required.
+ Assisting management with investigations and deviations related to sample management.
+ Collaborating with other departments to identity and implement process efficiencies.
+ Maintaining metrics for the Value Stream Cryo Operations group.
+ Facilitating cold chain transfers of material, as required.
+ Performs tasks for Cell Therapy products to support product Value Stream outputs according to Current Good Manufacturing Practices (cGMP's) following the current, approved Standard Operating Procedures (SOPs) and Work Instructions (WIs).
+ Maintains timing according to the production schedule to ensure on-time.
+ Cryopreservation support.
+ Cryopreserve Patient material daily, store and manage Inventory of material in LN2 storage locations.
+ Supports manual and electronic batch record executions, deviation investigations, and closure of CAPAs.
+ Maintains timing according to the production schedule to ensure on-time logistics.
+ Ensures all documentation is correct and addresses procedural/documentation errors expeditiously and effectively.
+ Work with management to ensure adequately trained personnel are available to perform all Value Stream Cryo Operations activities.
+ Records patient material handling data and information in a clear, concise, format according to proper GDPs.
+ Able to problem solve with minimal supervision.
+ Works in a team based, cross-functional environment to complete tasks required by shift schedule.
+ Available to work OT when business requires.
+ Willing to work staggered day shift hours.
Knowledge & Skills:
+ Experience with cold chain sample storage and transfer.
+ Knowledge of cGMP/FDA regulated industry.
+ Basic mathematical skills.
+ General understanding of cGMPs.
+ Technical writing capability.
+ Proficient in MS Office applications.
+ Inventory control and/or management.
+ Background to include an understanding of biology, chemistry, medical or clinical practices is a plus.
Basic Requirements:
+ Bachelor's degree
+ OR Associate/ Medical Technical degree and 0-2 years of Manufacturing or Operations experience.
+ OR High School diploma/GED and 2-4 years of Manufacturing experiences.
BMSCART, #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: R1586312
Updated: 2024-10-16 03:41:50.946 UTC
Location: Summit West-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
