Bristol Myers Squibb
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-usPosition Purpose Comply with all applicable legislations and regulations in support of worldwide transportation & distribution networks to meet the needs of Bristol Myers Squibb (BMS) clinical trials for Investigational Medicinal Products (IMPs), Pre-Approval Access (PAA) and/or Investigator Sponsored Research (ISR) and collaboration partners.
Key ResponsibilitiesMaintain and develop the management of IMP distribution infrastructure in support of the execution of investigational supply shipments to sites and 3rd party shipments.
Support the maintenance and management of BMS clinical trial operational activities outsourced to a global network of 3_PL, 4_PL clinical depots.
Oversight and main escalation contact of worldwide third-party vendors across a range of distribution activities.
Contribute to the development and optimization management of IMP warehouse operational framework, shipping and importation processes, strategy development and planning processes.
Development and maintenance of distribution/importation processes for new countries or with CRO/joint venture partners, including management of external vendor relationships.
Monitor performance of external clinical research organizations (CROs) as it relates to IMP handling, appropriately escalating compliance issues/training needs to CSL manager and CRO management.
Support, inform and advise on strategic outsourcing decision making, including RFP activity in alignment with global Logistics, Procurement, Contract Management, EHS, Security and Quality groups.
Contribute to continuous improvement projects in collaboration with internal/external cross-functional stakeholders.
Lead a range of CSCL project and activities also in compliance with the development of internal procedures related to quality/risk management investigations, returns, destruction, IATA and dangerous goods processes.
Degree RequirementsBachelor's Degree in relevant field (Logistics, Supply Chain, Science, Engineering, Business Administration)Experience Requirements Demonstrated experience in Logistics, Supply Chain, Pharmaceuticals, or related field.
Competency Requirements Working knowledge of ICH and GxP guidelines, with experience of application to investigational product distribution activities.
Demonstrated IT skill base, with operational knowledge of SAP, Microsoft Office applications and collaboration tools with proficiency in data handling and analysis.
Leadership, communication, and negotiation skills as well as transferable interpersonal skills with the ability to build effective relationships and networks at different levels.
Demonstrates a persistent, pro-active, flexible, and team-oriented work ethic.
Business level fluency in English.
Additional language(s) are a plus.
Demonstrated organizational skills with an ability to manage multiple projects simultaneously and to complete complex projects independently.
Reliable and ethically accountable team-player, with an ability to work independently and to take ownership of own deliverables and learning.
Customer minded, resilient, quality and detail orientated.
Travel and other requirements International travel on an as needed basis.
Work outside of UK office hours may be required to accommodate different time zones.
#LI-HybridIf 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 adastaffingsupport@bms.
com.
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.
Bristol Myers Squibb is Disability Confident - CommittedA UK Government schemeAbout the Company:
Bristol Myers Squibb.
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-usPosition Purpose Comply with all applicable legislations and regulations in support of worldwide transportation & distribution networks to meet the needs of Bristol Myers Squibb (BMS) clinical trials for Investigational Medicinal Products (IMPs), Pre-Approval Access (PAA) and/or Investigator Sponsored Research (ISR) and collaboration partners.
Key ResponsibilitiesMaintain and develop the management of IMP distribution infrastructure in support of the execution of investigational supply shipments to sites and 3rd party shipments.
Support the maintenance and management of BMS clinical trial operational activities outsourced to a global network of 3_PL, 4_PL clinical depots.
Oversight and main escalation contact of worldwide third-party vendors across a range of distribution activities.
Contribute to the development and optimization management of IMP warehouse operational framework, shipping and importation processes, strategy development and planning processes.
Development and maintenance of distribution/importation processes for new countries or with CRO/joint venture partners, including management of external vendor relationships.
Monitor performance of external clinical research organizations (CROs) as it relates to IMP handling, appropriately escalating compliance issues/training needs to CSL manager and CRO management.
Support, inform and advise on strategic outsourcing decision making, including RFP activity in alignment with global Logistics, Procurement, Contract Management, EHS, Security and Quality groups.
Contribute to continuous improvement projects in collaboration with internal/external cross-functional stakeholders.
Lead a range of CSCL project and activities also in compliance with the development of internal procedures related to quality/risk management investigations, returns, destruction, IATA and dangerous goods processes.
Degree RequirementsBachelor's Degree in relevant field (Logistics, Supply Chain, Science, Engineering, Business Administration)Experience Requirements Demonstrated experience in Logistics, Supply Chain, Pharmaceuticals, or related field.
Competency Requirements Working knowledge of ICH and GxP guidelines, with experience of application to investigational product distribution activities.
Demonstrated IT skill base, with operational knowledge of SAP, Microsoft Office applications and collaboration tools with proficiency in data handling and analysis.
Leadership, communication, and negotiation skills as well as transferable interpersonal skills with the ability to build effective relationships and networks at different levels.
Demonstrates a persistent, pro-active, flexible, and team-oriented work ethic.
Business level fluency in English.
Additional language(s) are a plus.
Demonstrated organizational skills with an ability to manage multiple projects simultaneously and to complete complex projects independently.
Reliable and ethically accountable team-player, with an ability to work independently and to take ownership of own deliverables and learning.
Customer minded, resilient, quality and detail orientated.
Travel and other requirements International travel on an as needed basis.
Work outside of UK office hours may be required to accommodate different time zones.
#LI-HybridIf 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 adastaffingsupport@bms.
com.
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.
Bristol Myers Squibb is Disability Confident - CommittedA UK Government schemeAbout the Company:
Bristol Myers Squibb.
Estimated Salary: $20 to $28 per hour based on qualifications.
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