Associate Director Regulatory Affairs

Harefield, England, United Kingdom · Regulatory Affairs

Description

MAIN PURPOSE:

The Regulatory Affairs Associate Director is responsible for management of the Lifecycle Team to develop and implement global regulatory strategy to maintain Norgine’s existing product licences and to integrate newly acquired/approved products into the team.

As a member of the Central Regulatory Affairs Management Team, the Regulatory Affairs Associate Director leads the lifecycle team, ensures the regulatory plans developed are aligned with the global product strategies for medicinal products and medical devices. In addition, advises on regulatory issues for marketed products and proactively mitigates the risk of obstacles and roadblocks, executing clear directions to manage priorities in line with business needs.

KEY RESPONSIBILITIES & ACCOUNTABILITIES:

Requirements

INDIVIDUAL REQUIREMENTS AND COMPETENCIES

SKILLS & KNOWLEDGE

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