Material Requirements Planner

Johnson & Johnson Co.

Geel

Ibrido

EUR 81.000 - 141.000

Tempo pieno

2 giorni fa
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Vantaggi offerti da questo lavoro

Annual bonus
Vacation days
Parental leave
Bereavement leave
Well-being reimbursement
Insurance plans

Descrizione del lavoro

Johnson & Johnson is seeking a Material Requirements Planner to ensure timely and cost-effective availability of raw materials for Pilot Plant production. You will translate the Master Production Schedule into detailed material requirements, manage supplier commitments, and guide the transition toward fully system-driven MRP.

Responsibilities include optimizing inventory, coordinating with Development Teams, and driving continuous improvement of MRP processes across Solids and Parenteral

Competenze

  • Minimum of a Bachelor’s degree in supply chain, operations, engineering, life sciences, or equivalent experience.
  • Minimum of 6 years of relevant supply chain, planning, procurement, or manufacturing experience.
  • APICS or equivalent supply chain certification is desirable.
  • Knowledge of clinical trials, clinical supply chains, material requirements planning, inventory management, and production scheduling.
  • Understanding of relevant manufacturing environments; experience across synthetics, proteins, or cell and gene modalities is beneficial.
  • Strong analytical and operational skills, with the ability to interpret exceptions, assess cost-benefit trade-offs, manage complexity, and make data-supported recommendations.
  • Results-oriented, adaptable, detail-focused, and able to operate with urgency in a volatile clinical environment.
  • Effective communicator and collaborator who can influence across functions and cultures, tailor messages to the audience, and challenge existing processes constructively.
  • Professional proficiency in English.
  • Experience with enterprise resource planning and advanced planning systems; SAP and OMP experience is preferred.
  • Strong working knowledge of Microsoft Excel.
  • Experience with applicable GMP, GCP, GDP, and quality-management processes.
  • Requires proficiency in English to communicate effectively and professionally; on-site minimum three days a week with two remote days.

Mansioni

  • Material planning and execution: Translate the Master Production Schedule into material requirements for the Pilot Plant; establish MRP processes and review purchase requisitions and MRP messages.
  • Balance lead times, flexibility, service, inventory, obsolescence risk, and budget targets; expedite critical materials to align with production plans.
  • Coordinate with Quality and warehouse teams on rejected or defective materials and supplier returns.
  • Support system-driven MRP design and implementation, including new materials, master data, planning parameters, qualification, and stakeholder communication.

Conoscenze

Analytical skills
English proficiency
Cross-functional collaboration
Microsoft Excel

Formazione

Bachelor’s degree in supply chain or related field
APICS certification desirable

Strumenti

SAP
OMP

Descrizione del lavoro

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.

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 Material Requirements 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: Ensure the timely and cost-effective availability of raw materials and components required to execute the Pilot Plant production plan. The role converts the Master Production Schedule and Development-driven demand into material requirements, manages supplier commitments and inventory, resolves constraints, and leads the transition toward fully system-driven MRP.

You will be responsible for:
  • Material planning and execution Translate the Master Production Schedule, detailed schedules, and development demand into material requirements for the assigned Pilot Plant. Take an active leadership role in fully establishing and maturing the MRP processes, as no formal process currently exists for Synth DP Pilot Plant Review purchase requisitions and MRP exception messages; confirm order quantities, dates, purchase orders, supplier acknowledgements, and committed delivery dates. Balance supplier lead times, clinical flexibility, service, inventory, obsolescence risk, and budget targets. Expedite critical materials and ensure delivery and release in time to execute the production plan, including accelerated first-in-human timelines. Collaborate closely with Material Managers and Development Teams across both Solids Development and Parenteral Development to ensure the timely availability of materials.
  • Risk, scenarios, and performance Assess material feasibility, model supply scenarios, identify constraints and trade-offs, and recommend resolution options to the end-to-end planning team. Manage abrupt plan changes with suppliers; promptly escalation that cannot be resolved within required timelines.
  • Inventory and operational coordination Design and maintain raw-material and component inventory processes, parameters, targets, and budget controls. Partner with warehouse teams to manage storage constraints and communicate future inventory impacts. Coordinate with Quality and warehouse teams on rejected or defective materials, including supplier returns or disposal.
  • Systems, launches, and improvement Support system design and implementation initiatives that enable fully system-driven MRP. Support introduction of new materials, including master data, planning parameters, qualification, ordering, and stakeholder communication. Drive continuous improvement of MRP processes, tools, data quality, and ways of working. Maintain effective relationships with New Products Introduction coordinator, Pilot Plant Operations, Detailed Scheduling, Quality, Warehouse, Procurement teams and Supply Network Planning, Track supplier service performance, investigate recurring issues, and coordinate corrective actions with Procurement, Pilot Plant Operations, Quality and Supply Network Planning.
Qualifications/Requirements
  • Minimum of a Bachelor’s degree in supply chain, operations, engineering, life sciences, or equivalent experience.
  • Minimum of 6 years of relevant supply chain, planning, procurement, or manufacturing experience.
  • APICS or equivalent supply chain certification is desirable.
  • Knowledge of clinical trials, clinical supply chains, material requirements planning, inventory management, and production scheduling.
  • Understanding of relevant manufacturing environments; experience across synthetics, proteins, or cell and gene modalities is beneficial.
  • Strong analytical and operational skills, with the ability to interpret exceptions, assess cost-benefit trade-offs, manage complexity, and make data-supported recommendations.
  • Results-oriented, adaptable, detail-focused, and able to operate with urgency in a volatile clinical environment.
  • Effective communicator and collaborator who can influence across functions and cultures, tailor messages to the audience, and challenge existing processes constructively.
  • Professional proficiency in English.
  • Experience with enterprise resource planning and advanced planning systems; SAP and OMP experience is preferred.
  • Strong working knowledge of Microsoft Excel.
  • Experience with applicable GMP, GCP, GDP, and quality-management processes.
  • Other requirements Requires proficiency in English (excellent written and verbal communication skills) to communicate effectively and professionally Requires the ability, through our flexible work policy, to work on-site a minimum of three days each week, with the option for two remote workdays each week.
Salary
  • The anticipated base pay range for this position is: €81,400.00 - €140,530.00
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.
  • 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.
  • 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.

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

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.

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