Johnson & Johnson is actively recruiting for a Manager, Clinical QA Program Lead, with flexible locations including the UK. The role focuses on driving audit strategies, execution of GCP audits, and inspection readiness to ensure regulatory compliance across therapeutic areas.
The position requires onsite work three days a week and collaboration across global teams. Ideal candidates will have 5+ years in a compliance/GxP environment, experience leading QA audit programs, and the ability to
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Global Clinical QA Program Lead Manager 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
