Johnson & Johnson in High Wycombe is seeking a Specialist, Process & Data Management (PDM) Program Expert to join the Quality Management & Digital (QM&D) organization. You will translate regulatory and quality requirements into compliant processes and learning solutions across global R&D teams.
The role involves collaboration with Therapeutic Areas, Clinical Development, Medical Safety, Regulatory Affairs, and R&D Quality to drive end-to-end process design, qualification activities, and training
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Hybrid PDM Program Specialist: Quality & Training in High Wycombe employer: Johnson & Johnson Innovative Medicine
At Johnson & Johnson Innovative Medicine, we pride ourselves on fostering a collaborative and inclusive work culture that empowers our employees to thrive. As a Regulatory Medical Writer II, you will benefit from our commitment to professional development, with ample opportunities for growth and learning in a dynamic environment. Located in the UK, our hybrid work model offers flexibility while allowing you to contribute to impactful projects that advance healthcare globally.
Contact Details:
Johnson & Johnson Innovative Medicine Recruitment Team
