E2E Supply Planner

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Essential Job Duties and Responsibilities

• Plans and manages the day-to-day activities of Clinical Supplies department such as packaging labeling assembling and shipping of clinical supplies used in clinical trials.

• Responsible for the departments clinical supplies database records maintenance protocol evaluation coding of samples and storage of approved materials.

• Complies to local regulatory and good manufacturing practices guidelines.

• Develop E2E supply plans for clinical compounds

• Identify the underlying assumptions for Kit/DP/API supply plan through the cS&OP process.

• Develop optimal end-to-end drug product and drug substance supply strategies for compounds that minimize waste while meeting the timelines and needs of the Clinical Trial Material supply plans.

• Create drug product and drug substance supply plans by aggregating clinical demand across different trials as well as non-clinical demands to ensure timely delivery testing and release of clinical batches.

• Provide information to the Supply Network Capacity Planners and Plant Schedulers to allow constrained master and/or detailed scheduling of batches in the CSC supply network in line with the trial requirements and in line with critical raw material and component availability.

• Drive structured improvements of functional processes in line with business or operational strategy.

• Ensure portfolio timelines and business performance goals objectives and metrics are achieved including consistency with GMP guidelines and all other compliance requirements

• Lead and/or supporting cross-functional and cross-departmental projects to improve business process/tools.

Minimum Qualification

• A minimum of 3 years of related experience is required.

• A minimum of a Bachelors Degree in business or science is required.

• Experience with several of the following supply planning processes: inventory management supply chain management supply planning production planning Lean and 6sigma systems (OMP SAP R/3 or ERP) other cross-functional supply chain processes is required.

• Strong leadership skills: Managing complexity conflict and ability to identify process gaps based on data or root cause analysis ability to predict risk/impact of supply related processes are required.

• Excellent communication negotiation and influencing skills with the ability to communicate clearly and appropriately to all levels of the organization in both written & oral forms is required.

• The ability to work independently multi-task and manage complexity is required.

• An innate aim to make the difference and achieve results is required.

• Continuous improvement in attitude and innovative thinking that will help see opportunities and related business needs is required.

• Insight into a clinical supply environment in a pharmaceutical industry its characteristics and constraints and Q&C requirements is preferred.

• Experience with GMP and/or Quality management systems and processes is preferred.

Other requirements

Focus on achievement and delivery of results with high sense of urgency

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The anticipated base pay range for this position is:

Benefits:

In addition to base pay we offer the following benefits*: an annual bonus with set target (% of pay) depending on pay grade / location where the actual amount is based on the employees and companies performance of the previous calendar year or sales commissions. Moreover we offer vacation days parental leave for a minimum of 12 weeks bereavement leave caregiver leave volunteer leave well-being reimbursement programs for financial physical and mental health. We also offer service anniversary and recognition awards and subject to the terms of their respective plans employees - and in some locations eligible dependents - can participate in several insurance plans. For more information visit Employee benefits Supporting well-being & career growth Johnson & Johnson Careers.

*This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change.

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