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Demand Planner, R&D
Taleo BE Princeton, NJ
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$75k-96k (estimate)
Full Time 1 Week Ago
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Taleo BE is Hiring a Demand Planner, R&D Near Princeton, NJ

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

The Demand & Operations Integration Lead is a key component of 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 Product Development (PD) supply operations are aligned in delivering bulk drug substance and drug product to satisfy the requirements of the development process.

Key Responsibilities

  • Create, develop, and manage demand plans in support of clinical programs and CMC Development Team activities across the R&D portfolio. Communicate regularly with sources of demand generation and solicit raw demand requirements from stakeholders.
  • Collaborate to ensure forecasts are developed for supported activities over a 24-month period. Collect and vet supporting assumptions, demand drivers, and risks associated with the raw demand requirements. 
  • Receive, assess, and manage changes to existing plans through a regular S&OP process. Communicate changes to requirements and identify demand requirements that are outside of currently budgeted or approved commitments.
  • Perform the inventory management function for drug product and drug substance materials supporting R&D clinical trials; allocate at the batch level, communicate the current and future inventory position in partnership with operations functions, and ensure inventory availability.
  • Participate or lead business process development efforts in support of nascent R&D Supply Chain functions. Contribute to the development of IT tools to enable R&D Supply Chain excellence.
  • Collaborate with Clinical Supply Chain 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.
  • Support CMC teams in conducting scenario planning exercises & develop and utilize tools to assess demand/supply implications to inform teams during strategy development process.
  • Interface and develop rapport with upstream and downstream stakeholders to enable efficient operations for demand requirements and the development of balanced outcomes.
  • Ensure plans are risk-adjusted in alignment with PD strategy by merging changing information sets into reasonable and defendable plans.

Qualifications & Experience

  • Bachelors with 5 years of experience in biopharmaceutical industry planning or an equivalent combination of education and experience may be considered; APICS certifications preferred
  • Prior experience within a supply chain function
  • Familiarity with operations in an S&OP process
  • Knowledge of regulatory and GMP frameworks related to clinical use of bulk drug substance/drug product
  • Knowledge of the drug development process and clinical trials
  • Demonstrated ability to work in the absence of concrete data by merging changing information sets into reasonable and defendable plans

#LI-Hybrid

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 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.

Job Summary

JOB TYPE

Full Time

SALARY

$75k-96k (estimate)

POST DATE

04/15/2024

EXPIRATION DATE

05/02/2024

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