E2E Supply Planner

Johnson & Johnson Co.; Geel; Sur place; EUR 61 000 - 98 000; Plein temps

Avantages offerts par ce poste

Annual bonus

Vacation days

Parental leave

Bereavement leave

Well-being programs

Résumé du poste

Johnson & Johnson is seeking an experienced E2E Clinical Supplies Planner for its Belgium operations. The role focuses on planning packaging, labeling, assembling, and shipping of clinical trial materials in Beerse/Antwerp, with emphasis on GMP compliance and on-time delivery.

You will build supply plans across trials, evaluate drug product and substance requirements, and collaborate with production schedulers to meet timelines while optimizing material usage.

Qualifications

• Bachelor’s Degree in business or science is required.
• 3+ years of related experience is required.
• Experience with supply planning processes (inventory, supply, production planning) is required.
• Knowledge of GMP and QA processes is preferred.
• Experience with SAP or ERP systems is preferred.

Responsabilités

• Develop end-to-end supply plans for clinical compounds across trials.
• Create drug product and drug substance supply plans aligning with trial requirements.
• Coordinate with Supply Network Capacity Planners and Plant Schedulers for master and detailed scheduling.
• Drive process improvements and ensure GMP compliance across activities.

Connaissances

Supply planning

Inventory management

Lean & Six Sigma

Leadership

Communication

Cross-functional collaboration

Problem solving

Risk assessment

Formation

Bachelor’s Degree in business or science

Outils

SAP R/3

ERP systems

OMP

Description du poste

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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-109449, United States of America R-108785 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: About Innovative Medicine Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at https://www.jnj.com/innovative-medicine We are searching for the best talent for E2E Supply Planner.

Candidates must already have authorization to work in the country of employment. Immigration sponsorship and relocation support are not available for this position. Candidates authorized to work pursuant to a short-term status (e.g., F-1) who require future immigration sponsorship are not eligible.

Purpose

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 department's clinical supplies database records maintenance, protocol evaluation, coding of samples, and storage of approved materials. Complies to local regulatory and good manufacturing practices guidelines.

You will be responsible for:

• Develop E2E supply plans for clinical compounds
• Identify the underlying assumptions for Kit/DP/API supply plan through the cSOP 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.

Qualifications/Requirements:

• A minimum of a Bachelor’s Degree in business or science is required.
• A minimum of 3 years of related experience 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

Required Skills

The anticipated base pay range for this position is: €61,200.00 - €98,210.00

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 location’s eligible dependents - can participate in several insurance plans.

For more information, visit Employee benefits | Supporting well-being & career growth | Johnson & Johnson Careers.

Company Culture

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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 https://www.jnj.com/. Our Credo calls on us to respect the dignity of every individual and create an environment for all people to thrive.

Throughout the recruitment process - from application through hiring - we are committed to providing reasonable accommodations/adjustments for qualified candidates with disabilities. If you need support at any stage of the recruitment process, please complete our candidate accommodation request form so we can assist you.