Global PDM Program Lead: Quality & Data Management

6010-Biosense Webster Inc. Legal Entity; High Wycombe; On-site; GBP 60,000 - 90,000; Full time

Job summary

Johnson & Johnson in the United Kingdom seeks a Specialist, Process & Data Management (PDM) Program Expert to support QM&D. The role shapes regulatory-compliant processes, learning content, and qualification solutions across global R&D, coordinating with Regulatory Affairs and Medical Safety teams.

You will translate evolving requirements into practical, compliant solutions, drive end-to-end process design, and enable efficient R&D activities within a matrix organization.

Qualifications

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

Responsibilities

• Leading ARR and Quality Framework Integration initiatives.
• Developing and implementing compliant end-to-end processes.
• Creating and maintaining training and qualification materials within the GxP QMS.
• Performing requirement comparison and integration across the Quality Management System.
• Participating in content management and qualification transformation initiatives.
• Coordinating with Therapeutic Areas, Clinical Development, Medical Safety, Regulatory Affairs, and R&D Quality.

Skills

Regulatory compliance knowledge

Global development collaboration

Process design

Training design

Quality Management System

Data-centric thinking

Communication skills

Attention to detail

Cross-functional teamwork

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 in the United Kingdom seeks a Specialist, Process & Data Management (PDM) Program Expert to support QM&D. The role shapes regulatory-compliant processes, learning content, and qualification solutions across global R&D, coordinating with Regulatory Affairs and Medical Safety teams.

You will translate evolving requirements into practical, compliant solutions, drive end-to-end process design, and enable efficient R&D activities within a matrix organization.