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Years of Experience
Date Last Verified
Director/Senior Director, Regulatory Science & Policy Lead for Consumer Healthcare GBU Duties: Develop effective and systematic approaches to bring functional excellence to Regulatory Intelligence and Policy across Global Business Unit with emphasis on key markets. Drive best practices and excellence in execution within the department and cross-functionally. Contribute to the creation, standardization and implementation of systems/processes to monitor the regulatory environment for changes, and to work with subject matter experts within the company to assess impact on products and growth initiatives. Monitor, identify and assess regulatory intelligence and policy for relevance and impact to company’s internal processes, CHC product development and or regulatory and corporate strategies. Coordinate and involve stakeholders across functions to effectively communicate impact and bring awareness of business critical issues for informed decision making. Provide leadership and guidance on Policy matters. Routinely coordinate and communicate regulatory policy activities and work products to relevant stakeholders, strategize and present action plan to address/mitigate future issues. Serve as key liaison, and represent as assigned, maintain a view of Trade Association involvement and activities across the globe and look for opportunities to encourage new and develop existing Trade Associations. Manage and engage in think tanks, advocacy organizations and with regulatory authorities, and guide the strategy for and execution of these interactions in the field with emphasis on key markets. Build a culture of awareness of local regulatory themes by sharing local regulatory information, and plans for regulatory interactions across the regulatory organization.
Qualification and Experience
Qualifications: Advance life science degree (PhD, MD preferred) or law degree (JD Degree) with industry or government experience. 5-10 (depending on level) years’ experience in the field and/or related areas with proven expertise in Regulatory environment. Experience working with senior-level members or officials of trade associations or other key groups that influence regional policies in the CHC field with emphasis on key markets. Experience in participating in, or supporting, global product development or other cross-functional teams. Existing relationship with local/regional government legislators, trade associations, committees, administrative staff or other key parties or influencers in the CHC field with emphasis on key CHC markets. Significant understanding of the prescription and non-prescription drugs, herbal medicines, vitamins and mineral supplements, food supplements/nutraceuticals, medical devices, digital technologies, cosmetics development and commercialization process. Good level of spoken and written English. Ability to work in a matrix organization. Strong business and customer orientation. High standards of integrity.
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