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Job Description Summary
The Associate Director, Regulatory Affairs, Specimen Management (SM) reports directly to the Vice President, Regulatory Affairs, Specimen Management. This position is responsible for regulatory activities and personnel supporting the Specimen Acquisition (SA) business growth and sustaining agenda. The role includes responsibilities for directing and evolving the regulatory strategy for the SA Platform, interacting with regulatory authorities and Notified Bodies to ensure SA’s growth and continued right to operate, supporting SA New Product Development and sustaining efforts, identifying and championing innovative regulatory approaches, collaborating within the RA function and cross-functionally to drive success, and leading and inspiring a team of regulatory affairs associates. This role will directly engage with both the SM RA Leadership Team and the SA Platform Leadership Team.Job Description Summary
The Associate Director, Regulatory Affairs, Specimen Management (SM) reports directly to the Vice President, Regulatory Affairs, Specimen Management. This position is responsible for regulatory activities and personnel supporting the Specimen Acquisition (SA) business growth and sustaining agenda. The role includes responsibilities for directing and evolving the regulatory strategy for the SA Platform, interacting with regulatory authorities and Notified Bodies to ensure SA’s growth and continued right to operate, supporting SA New Product Development and sustaining efforts, identifying and championing innovative regulatory approaches, collaborating within the RA function and cross-functionally to drive success, and leading and inspiring a team of regulatory affairs associates. This role will directly engage with both the SM RA Leadership Team and the SA Platform Leadership Team. Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Become a maker of possible with us. BD’s Specimen Management Regulatory Affairs organization is the keystone of Specimen Management’s product registration efforts, connecting internal and external stakeholders to deliver safe, effective, and innovative diagnostic collection and care devices to patients and customers in alignment with business priorities and global regulations. About The Role In this role you will lead regulatory strategies and ensure compliance, driving growth and innovation in our team. Key Responsibilities Will IncludeReferrals increase your chances of interviewing at BD by 2x
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