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Demand & Operations Integration Lead

Company

Bristol Myers Squibb

Address Princeton, NJ, United States
Employment type FULL_TIME
Salary
Category Pharmaceutical Manufacturing
Expires 2023-08-27
Posted at 9 months ago
Job Description
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.


Position Summary


This position is a key component of the R&D Supply Chain, and acts as a central point of contact for portfolio asset teams during demand planning, in support of the R&D clinical trial book of work and CMC development activities. This position is accountable for the development, maintenance and communication of demand plans to ensure that PD supply operations are aligned in delivering bulk drug substance and drug product to satisfy the requirements of the development process.


Key Responsibilities


  • Collaborate with the Clinical Supply Chain organization to ensure that bulk drug forecasts are incorporated into demand plans and adequately represent clinical requirements. Translate product demands between value chain levels by understanding product presentation requirements and bill of material relationships.
  • Participate and/or lead business process development efforts in support of a nascent R&D Supply Chain function. Contribute to the development of information technology tools which will enable R&D Supply Chain excellence, part of the PD strategy.
  • Co-lead the business process and meeting sets by which demand plans are communicated to supply operations and become aligned with supportable corresponding supply plans. Receive, assess and manage changes to existing plans and triage these with rigor through a change management process. Communicate changes to requirements as well as to existing plans with urgency and transparency. Identify demand requirements that are outside of currently budgeted and/or approved commitments.
  • Support CMC teams in conducting scenario planning exercises during asset strategy development. Develop and utilize tools to aid in the assessment of demand and supply implications and inform teams during the development of strategic options.
  • Perform the inventory management function for drug product and drug substance materials supporting R&D clinical trials. As part of this responsibility, allocate at the batch level, communicate the current and forward looking inventory position in partnership with operations functions and ensure inventory availability through batch level use date management.
  • Create and manage demand plans in support of clinical programs and CMC Development Team activities across the R&D portfolio. Develop an understanding of CMC and clinical strategy to aid in the development of relevant demand plans. Communicate regularly with sources of demand generation and solicit raw demand requirements from stakeholders. Through collaboration, ensure forecasts are developed for supported activities over a 24 month rolling time horizon. Collect and vet supporting assumptions, demand drivers and risks associated with the raw demand requirements. Aggregate demand across stakeholders and time periods in the development of supportable demand plans.


Qualifications & Experience


  • Prior experience within a supply chain function; familiarity and operation within an S&OP process; knowledge of regulatory and GMP frameworks related to clinical use of bulk drug substance and drug product; knowledge of the drug development process and clinical trials; APICS certifications; 5-7 years biopharmaceuticals industry planning experience.
  • Ability to maintain a strategic view while operating at a level of fine detail; correlate portfolio priorities and strategy to daily operations and decision making within the supply chain environment.
  • Face multiple upstream and downstream stakeholders, and through regular interactions, develop trusted relationships to enable efficient operations; leverage a wide sphere of influence; pressure test demand requirements and supply constraints constructively and negotiate bi-directionally to develop balanced outcomes.
  • Operate with a high degree of connectedness, transparency and clarity to ensure common understanding of requirements, issues and actions; listen to stakeholders and distill information into pertinent and actionable content.
  • Demonstrate a nimble nature to adapt to the pace and dynamic nature of an R&D environment; process data, information and feedback with speed and communicate outcomes, alternatives and actions plans with appropriate urgency.
  • Ensure plans are risk adjusted and in alignment with PD strategy and priorities; demonstrate comfort working in the absence of concrete data and information; merge both firm and changing information sets into reasonable and defendable plans.


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


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.