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Katalyst Healthcares & Life Sciences

Regulatory Affairs Consultant

Katalyst Healthcares & Life Sciences, Detroit, Michigan, United States, 48201

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Responsibilities: Develop global regulatory strategies for medical device products to meet business objectives and collaborate across a matrixed organization to ensure global success of products registration. Participate on product development teams, providing regulatory strategies, timelines, and direction. Reviews and approvals of technical documentation. Negotiate with regulatory authorities.