Global PDM Program Expert: Quality & Training

Johnson & Johnson Innovative Medicine; Breda; On-site; EUR 60,000 - 96,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Parental leave

Well-being reimbursement

Job summary

Johnson & Johnson Innovative Medicine is seeking a Specialist, Process & Data Management (PDM) Program Expert to join the Quality Management & Digital (QM&D) organization. The role supports compliant end-to-end processes, training materials, and qualification solutions across global R&D and regulatory functions.

You will collaborate with Therapeutic Areas, Global Development, Medical Safety, Regulatory Affairs, and R&D Quality to translate requirements into integrated processes and learning

Qualifications

• Knowledge of global pre-clinical and clinical compliance regulations and guidelines.
• Awareness of regulatory and legal requirements within the life sciences industry.
• Experience contributing to process improvement, procedural integration, and qualification activities.

Responsibilities

• Leading ARR and Quality Framework Integration initiatives.
• Driving end-to-end process development and integration.
• Developing and maintaining training and qualification materials within the GxP framework.
• Participating in content management and qualification transformation initiatives.

Skills

Quality management

Collaboration

Regulatory knowledge

Process improvement

Training design

Communication skills

Project management

Problem solving

Education

Bachelor’s degree in Science, Business, or related field

Tools

Microsoft Office

Project management tools

Process mapping tools

AI concepts awareness

Job description

Johnson & Johnson Innovative Medicine is seeking a Specialist, Process & Data Management (PDM) Program Expert to join the Quality Management & Digital (QM&D) organization. The role supports compliant end-to-end processes, training materials, and qualification solutions across global R&D and regulatory functions.

You will collaborate with Therapeutic Areas, Global Development, Medical Safety, Regulatory Affairs, and R&D Quality to translate requirements into integrated processes and learning