Specialist, Production Planning
Princeton, New Jersey, United States
Job Summary
Occupation
Transportation and Logistics
Specialty
Specialist
Location
08901, New Brunswick, New Jersey, United States
Visa Sponsorship
No
Job Description
Last Update:
1/11/24
Working with Us Challenging. Meaningful. Life-changing. Those arent 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. Youll 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 Description:
Supports central planning function in Clinical Supply Operations (CSO) R&D supply chain. The incumbent is responsible, on a monthly cycle, for supporting the oral solid dose and parenteral dosage form drug product via multiple transactional related requirements, including SAP Material No generation and Material Master set-up, Development BOMS, starting material procurement and availability, M2M transfers and finished DP Batch Release milestones.
Participates as key DP supply representative in DOI (Development and Operations Integration) processes including Demand Alignment Meetings and Interface Forums.
Collaborates with CSO Clinical Supply Services group, Operations Quality and other PD functions to facilitate raw material lead times; Further, assure Product Batches support FPFV targets and complied with release schedules defined on the Master Production Plan driving batches to deliver 93% compliance (as defined by normalized metrics) against finished supply delivery targets established within the Master Production Plan.
Support operations readiness meetings where key deliverables by CMC development and operations are reviewed to enable production against projected timelines.
Support On Site Compounding strategy by monitoring new requirements, checking that all supporting data properly input and track operations activities from Firm of order to Shipment of materials.
Support maintenance of GPS batches for clinical need via upload of supporting docs to Quality.
Position Requirements:
BS in Pharmacy/Chemistry or Industrial/Chemical Engineering or Business focus.
1-3 years experience in Supply Chain, Production Planning, Business Operations or a related environment. Must demonstrate a high level of performance in these areas.
Knowledge of SAP planning transactions.
Basic understanding of solid/ parenteral dosage form processes
Must be an effective communicator with the ability to collaborate across multiple levels in the organization. Must be good at follow up and ensure that time lines are met.
Must have good leadership skills and the ability to lead projects/tasks.
If you come across a role that intrigues you but doesnt 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 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.
COVID-19 Information To protect the safety of our workforce, customers, patients and communities, the policy of the Company requires all employees and workers in the U.S. and Puerto Rico to be fully vaccinated against COVID-19, unless they have received an exception based on an approved request for a medical or religious reasonable accommodation. Therefore, all BMS applicants seeking a role located in the U.S. and Puerto Rico must confirm that they have already received or are willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and condition of employment. This requirement is subject to state and local law restrictions and may not be applicable to employees working in certain jurisdictions such as Montana. This requirement is also subject to discussions with collective bargaining representatives in the U.S.
BMS is dedicated to ensuring that people with disabilities can perform complex functions through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an accommodation prior to accepting a job offer. If you require reasonable accommodation 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 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 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 Description:
Supports central planning function in Clinical Supply Operations (CSO) R&D supply chain. The incumbent is responsible, on a monthly cycle, for supporting the oral solid dose and parenteral dosage form drug product via multiple transactional related requirements, including SAP Material No generation and Material Master set-up, Development BOMS, starting material procurement and availability, M2M transfers and finished DP Batch Release milestones.
Participates as key DP supply representative in DOI (Development and Operations Integration) processes including Demand Alignment Meetings and Interface Forums.
Collaborates with CSO Clinical Supply Services group, Operations Quality and other PD functions to facilitate raw material lead times; Further, assure Product Batches support FPFV targets and complied with release schedules defined on the Master Production Plan driving batches to deliver 93% compliance (as defined by normalized metrics) against finished supply delivery targets established within the Master Production Plan.
Support operations readiness meetings where key deliverables by CMC development and operations are reviewed to enable production against projected timelines.
Support On Site Compounding strategy by monitoring new requirements, checking that all supporting data properly input and track operations activities from Firm of order to Shipment of materials.
Support maintenance of GPS batches for clinical need via upload of supporting docs to Quality.
Position Requirements:
BS in Pharmacy/Chemistry or Industrial/Chemical Engineering or Business focus.
1-3 years experience in Supply Chain, Production Planning, Business Operations or a related environment. Must demonstrate a high level of performance in these areas.
Knowledge of SAP planning transactions.
Basic understanding of solid/ parenteral dosage form processes
Must be an effective communicator with the ability to collaborate across multiple levels in the organization. Must be good at follow up and ensure that time lines are met.
Must have good leadership skills and the ability to lead projects/tasks.
If you come across a role that intrigues you but doesnt 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 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.
COVID-19 Information To protect the safety of our workforce, customers, patients and communities, the policy of the Company requires all employees and workers in the U.S. and Puerto Rico to be fully vaccinated against COVID-19, unless they have received an exception based on an approved request for a medical or religious reasonable accommodation. Therefore, all BMS applicants seeking a role located in the U.S. and Puerto Rico must confirm that they have already received or are willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and condition of employment. This requirement is subject to state and local law restrictions and may not be applicable to employees working in certain jurisdictions such as Montana. This requirement is also subject to discussions with collective bargaining representatives in the U.S.
BMS is dedicated to ensuring that people with disabilities can perform complex functions through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an accommodation prior to accepting a job offer. If you require reasonable accommodation 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 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.