Associate Director, Global Regulatory Affairs Labe

at Incyte Corporation in Wilmington, Delaware, United States

Job Description

Overview   Incyte is a biopharmaceutical company focused on the discovery, development, and commercialization of novel medicines to meet serious unmet medical needs in oncology and inflammation and autoimmunity. Incyte is committed to the rigorous pursuit of research and development excellence to improve the lives of patients, make a difference in health care, and build sustainable value. The Company strives to discover and develop first-in-class and best-in-class medicines-advancing a diverse portfolio of large and small molecules. Job Summary The Associate Director, Global Regulatory Affairs Labeling, will be responsible for regulatory support in the area of product labeling. This position reports to the Director, Global Regulatory Affairs Labeling and will be responsible for creating, updating, and maintaining labeling documents throughout the product lifecycle, with primary focus on Company Core Data Sheets and regional/local labels for products marketed globally. This position will help maintain records for labeling changes and communicate labeling changes to stakeholders. As needed, this position will also support the implementation of process improvement changes to increase the efficiency and effectiveness of labeling processes. This role may collaborate with external partners. Key responsibilities *Leads cross-functional teams in the development, revision, review, and approval of Company Core Data Sheet and regional/local product labeling documents, for assigned products, in line with regulatory and internal standards and guidelines. *Provides labeling expertise and guidance to teams about labeling content, processes, and timelines. *In collaboration with Supply Chain, contributes to the development of new and updated packaging mock-ups and artwork for submission purposes. *Serves as the point of contact on Global Regulatory Affairs sub-teams to ensure delivery of labeling documents that meet quality, compliance, and regulatory labeling standards, to support timely regulatory submissions for assigned products. *Ensures high quality and compliant labeling documents. *Contributes to the continuous improvement of the end-to-end labeling process. *Supports internal and external audits/inspections as a labeling subject matter expert. Qualifications *Bachelor's degree in a scientific discipline. Advanced degree preferred (MS, PharmD, PhD). *Relevant experience in the pharmaceutical industry including 4+ years of direct regulatory labeling experience. *US labeling experience required; ex-US labeling experience preferred. *Ability to guide cross-functional teams (including senior management) and drive consensus to address labeling issues. *Self-starter with an ability to assimilate clinical and scientific information and present it concisely. Understanding of medical concepts and terminology. *Strong project management skills with the ability to handle multiple projects and prioritize work accordingly. Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required. Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer. We Respect Your Privacy Learn more at: The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate.   During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process . You may have the right to access, delete, restrict, edit, move, or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work. You can learn more about Incyte's data protection practices . By accessing this link you can learn about the types of personal data we collect, how we use it, whether collection and processing is optional, sources of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incyte's data protection officer, and your supervisory authority (if applicable). Please contact... For full info follow application link.   We appreciate, celebrate, and thrive on one another’s differences and strengths and are proud to be an Equal Opportunity Employer. By valuing diversity of backgrounds and perspectives and prohibiting all forms of harassment, we are able to promote a collaborative and innovative work environment in which everybody can contribute to their fullest potential.  


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Job Posting: 1258255

Posted On: Apr 10, 2024

Updated On: May 10, 2024

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