PDM Program Specialist – Quality & Data

7555-Janssen Pharmaceutica NV Legal Entity; Geel; Sur place; EUR 60 000 - 96 000; Plein temps

Résumé du poste

Johnson & Johnson is seeking a Specialist, Process & Data Management (PDM) Program Expert to join the QM&D organization. The role spans multiple countries, contributing to quality processes, training, and qualification solutions within the global R&D lifecycle.

You will translate regulatory requirements into practical, compliant solutions and work with cross-functional teams to enable efficient, compliant R&D activities.

Qualifications

• Bachelor’s degree in Science, Business, or a related field.
• Minimum 1–3 years of experience in a medium-to-large matrix organization.
• Minimum 1 year in a pharmaceutical, medical device, healthcare, compliance, or related R&D environment.
• Minimum 1 year of experience in process design, training design, qualification management, or a related field.

Responsabilités

• Leading and contributing to ARR (Adopting Regulatory Requirements) and Quality Framework Integration initiatives.
• Driving assessment, analysis, development, implementation, and integration of compliant end-to-end processes.
• Developing and maintaining training and qualification materials within the GxP Quality Management Framework.
• Performing requirement comparison, assessment, and integration activities across the Quality Management System.
• Participating in content management and qualification transformation initiatives, including programs such as Aris CCL.

Connaissances

Collaboration

Quality systems

Regulatory awareness

Data management

Formation

Bachelor’s degree in Science/Business or related field

Outils

Microsoft Office

Project management tools

Process mapping tools

Description du poste

Johnson & Johnson is seeking a Specialist, Process & Data Management (PDM) Program Expert to join the QM&D organization. The role spans multiple countries, contributing to quality processes, training, and qualification solutions within the global R&D lifecycle.

You will translate regulatory requirements into practical, compliant solutions and work with cross-functional teams to enable efficient, compliant R&D activities.