Senior Analyst, R&D Master Data

Johnson & Johnson Innovative Medicine

Beerse

Sur place

EUR 73 000 - 115 000

Plein temps

Il y a 3 jours
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Avantages offerts par ce poste

Annual bonus
Vacation days
Parental leave

Résumé du poste

Johnson & Johnson Innovative Medicine is seeking a Senior Analyst for R&D Central Master Data. You will own the creation, governance, and quality of clinical finished goods master data in SAP S/4HANA and related systems, partnering with cross-functional teams to support trial planning, manufacturing, packaging, and forecasting.

You will act as SME for master data processes, drive data quality, and contribute to continuous improvements while ensuring regulatory compliance and system integrity

Qualifications

  • Bachelor’s degree required; advanced degree preferred.
  • Minimum of six (6) years of experience in clinical supply chain or related functions.
  • Experience with SAP S/4HANA and Material Master concepts.
  • Experience with ERP implementations, data migration, or system deployments.
  • Knowledge of data governance and data quality management.

Responsabilités

  • Lead the creation, maintenance, governance of clinical finished goods master data in SAP S/4HANA and related planning systems.
  • Ensure master data accuracy, completeness, and regulatory compliance.
  • Define and improve data governance processes, standards, and controls.
  • Serve as SME and Super User for SAP S/4HANA master data in clinical supply operations.
  • Provide technical guidance, troubleshooting, and issue resolution.
  • Support development, testing, and implementation of new master data requirements and system enhancements.
  • Collaborate with IT and business teams to design and implement system changes.
  • Translate clinical trial requirements into scalable data solutions.
  • Maintain understanding of clinical supply chain processes to advise on best practices.
  • Support user access management and system administration in planning systems.
  • Monitor data quality metrics and communicate status to stakeholders.
  • Develop reports, dashboards, and analytics for decision-making.
  • Lead training initiatives and mentor team members.
  • Drive continuous improvement in master data governance and data quality.

Connaissances

Analytical reasoning
Clinical supply chain
Clinical trials operations
Communication
Distribution management
Inventory control
Inventory optimization
Laboratory operations
Mentorship
Organizing
Package & labeling regulations
Problem solving
Process improvements
Project management
Research & development
Stakeholder engagement
SOP

Formation

Bachelor's degree
Advanced degree

Outils

SAP S/4HANA

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.

Job Function

R&D Operations

Job Sub Function

Clinical Supply Operations

Job Category

Professional

All Job Posting Locations:

Beerse, Antwerp, Belgium

Job Description

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 Senior Analyst, R&D Central Master Data

Purpose: The Senior Analyst, R&D Central Master Data, is responsible for the creation, maintenance, governance, and quality oversight of clinical finished goods master data in SAP S/4HANA and associated clinical supply planning systems.

This role partners closely with Clinical Supply Chain, Trial Supply Leads, End-to-End Supply Planners, Supply Network Planners, Clinical Operations, Quality and other stakeholders to ensure master data accurately supports clinical trial planning, manufacturing, packaging, distribution, and forecasting activities.

The individual will act as a subject matter expert for clinical supply master data processes, provide technical support for related systems, drive data quality and compliance, develop reporting and analytics, and contribute to continuous process improvement initiatives.

You Will Be Responsible For
  • Lead the creation, maintenance, validation, and governance of clinical finished goods master data in SAP S/4HANA and related planning systems.
  • Ensure master data accuracy, completeness, consistency, and compliance with established business processes, data standards, and regulatory requirements.
  • Define, maintain, and continuously improve master data governance processes, procedures, standards, and controls.
  • Serve as the functional Subject Matter Expert (SME) and Super User for SAP S/4HANA master data supporting clinical supply operations.
  • Provide technical guidance, troubleshooting support, and issue resolution related to SAP S/4HANA master data and supply planning processes.
  • Support the development, testing, and implementation of new master data requirements, system enhancements, and process improvements.
  • Partner with business and IT teams to evaluate, design, and implement system changes impacting master data processes.
  • Collaborate with cross-functional stakeholders to understand clinical trial requirements and translate business needs into scalable master data and system solutions.
  • Maintain a deep understanding of clinical supply chain processes, trial design considerations, and planning system functionality to provide effective recommendations and support.
  • Support user access management and system administration activities within clinical supply planning systems.
  • Monitor data quality metrics, process compliance, and milestone completion, and communicate status, risks, and recommendations to business stakeholders.
  • Develop, maintain, and deliver reports, dashboards, and analytics to support operational and strategic decision-making.
  • Lead training initiatives, develop and maintain training materials, and drive adoption of SAP S/4HANA master data processes and best practices.
  • Mentor team members provide technical coaching, and support onboarding and capability development for new team members.
  • Drive continuous improvement initiatives focused on master data governance, data quality, process simplification, operational efficiency, and system adoption.
  • Ensure adherence to regulatory, quality, compliance, and company policies and standards.
Qualifications / Requirements
  • Bachelor’s degree required; advanced degree preferred.
  • Minimum of six (6) years of experience in clinical supply chain, supply chain operations, clinical operations, master data management, or related business functions.
  • Experience working with SAP S/4HANA, including Material Master and other supply chain master data concepts.
  • Experience supporting ERP implementations, data migration projects, or system deployments.
  • Experience with data governance, data quality management, data stewardship, and process improvement initiatives.
  • Knowledge of enterprise data governance frameworks and master data management best practices.
  • Strong analytical, problem-solving, and organizational skills.
  • Demonstrated ability to collaborate effectively across functions and build strong stakeholder relationships.
  • Ability to work in a complex, global, cross-functional environment.
  • Strong written, verbal, and presentation communication skills.
  • Proficiency in Microsoft Excel, including pivot tables, data analysis, reporting, and data validation activities.
Required Skills
Preferred Skills:

Analytical Reasoning, Clinical Supply Chain, Clinical Trials Operations, Communication, Distribution Management, Inventory Control, Inventory Optimization, Laboratory Operations, Mentorship, Organizing, Package and Labeling Regulations, Problem Solving, Process Improvements, Project Management, Research and Development, Stakeholder Engagement, Standard Operating Procedure (SOP)

The Anticipated Base Pay Range For This Position Is

€72,500.00 - €115,230.00

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 location’s 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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