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Caring for the world, one person at a time... inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a bill...
You are responsible to provide regulatory input on submission documents to ensure compliance with regulatory requirements. You may also provide regulatory support for and appropriate follow-up to inspections, audits and issue management. You act as the regulatory representative on specific multi-disciplinary teams as well as provide support in portfolio optimization activities. A more detailed description of the role requirements follows:
Strategic and tactical input in Post-approval and Life cycle management including Portfolio optimization and issue management
Liaison with Regulatory Agencies and Local Operating Companies, in support of the Regulatory Liaison to:
Input in document and process development
Clinical Trial Applications (CTA) and Post approval commitments
Health Authority Submissions and communicationsQualifications
Education and Experience:
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