Senior E2E Supply Planner
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at jnj.com.
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.
We provide an inclusive work environment where each person is considered as an individual.
At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s): Belgium R-105377, United States of America R-108331 Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Job Function: R&D Operations
Job Sub Function: Clinical Supply Operations
Job Category: Professional
All Job Posting Locations: Beerse, Antwerp, Belgium
Job Description
Objectives and Responsibilities
This individual contributor is responsible for planning the Pack & Label and Distribution activities of Patient Kits and DP (Drug Product) and API (Active Pharmaceutical Ingredient) to meet First-Patient-In (FPI) date and consistently meet Successful Patient Dose target throughout the lifecycle of a J&J Pharma R&D trial, within budget. Generally, the focus is on large, complex studies and compounds. These DP, Kit Supply & Inventory planning processes are the input to the cSOP Demand Review process, kick-off the cSOP cycle and at the same time trigger the execution of the P&L and Distribution plans.
Main Duties / Additional Duties / Sphere of authority
Planning System Configuration (OMP & SAP)
In study design phase seamlessly transition from CSI the planning related activities. With support from the Systems and RTSM team provide Master Data, configure distribution networks in the relevant Kit and DP planning systems and set planning and inventory parameters.
Set and own the trial supply budget for P&L and Distribution and work with Logistics to ensure budgets are met or adjusted in relevant systems. Inform CSI of budget status, risks or significant changes, including rationale Adapt supply strategies (SC configuration, planning parameters) in view of changes in trial execution or protocol.
Demand planning support Verify forecast is transferred correctly in OMP from 4C Supply Network planning Develop supply strategies to meet clinical plans while optimizing drug overage
Net Requirements planning: Ensure supply planning is adapted to latest forecast recruitment rates and inventory strategy.
Distribution planning: Utilize business tools to set and actively manage inventory targets at depots and sites and provide guidance to TSM to ensure on-time delivery with minimal overage of clinical supplies cSOP meetings
Responsible for making transparent any study risks via the cSOP process.
Responsible for identifying and developing scenario analysis to drive/support decision making through the cSOP process.
Escalation point and interface with the management team via Executive cSOP, with some guidance from Team Lead Attend the Kit RR meeting as needed to ensure P&L campaigns are QP/QP released per OTD date
Work independently with limited coaching, also in situations of high workload
Support continuous improvement initiatives.
Act as role model within team for use of core planning processes and proper use of planning systems and tools
With some guidance, responsible for managing Supply and Inventory issue escalation and resolution at the study and compound level.
Strong analytical and planning skills required: Manage complexity and be able to identify process gaps based on data or root cause analysis, be able to predict risk/impact of demand & supply related processes
Gathers diverse viewpoints and able to influence key stakeholders within the Clinical Supply Chain, and other key cross functional partners
Excellent written and verbal communication skills, able to communicate clearly, making the complex clear and compelling to all levels of the organization in both written and oral forms.
Thorough understanding of clinical trials and underlying dynamics to optimize global DP, P&L and Distribution processes and interdepen