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Senior Manager, Regulatory Operations
1 month ago
Sumitomo Pharma Senior Manager, Regulatory Operations Madison, Wisconsin Apply Now Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the U.S. (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma Canada, Inc.) and Europe (Sumitomo Pharma Switzerland GmbH) focused on addressing patient needs in oncology, urology, women's health, rare diseases, psychiatry & neurology, and cell & gene therapies. For more information on SMPA, visit our website here or follow us on LinkedIn here . Job Overview We are currently seeking a dynamic, highly motivated, and experienced individual for the position of Senior Manager, Regulatory Operations. For assigned projects, the Senior Manager of Regulatory Operations is responsible for managing all Regulatory Affairs activities involving compilation, publishing, distribution, and archiving of health authority submissions. Job Duties and Responsibilities Overseeing the external Submission Managers with defining submission outlines, content, format, and quality requirements for electronic submissions. Managing external submission Managers to ensure accurate and timely management of tracking, compiling, publishing, quality checking, dispatching, and archiving of Health Authority submissions. Facilitating submission preparation via completion of forms and creation of cover letters. Representing Regulatory Operations on project teams for matters relating to electronic (and paper) submissions. Overseeing external Submission Managers to ensure accurate printing, distributing, and archiving all incoming and outgoing communications with FDA and international counterpart agencies. Leading the implementation, validation, and operation of eCTD and electronic document management systems and other publishing and submissions technology projects. Leading the development, refinement, and implementation of internal processes, procedures, work instructions, and training programs for submission production and operational support activities. Understanding evolving Health Authority (HA) standards and procedures for regulatory submissions. Coordinating and consulting with other departments on the content, review, and assembly of regulatory documentation. Assisting in the creation of regulatory project plans and timelines for multiple projects or developmental programs. Leading the training of appropriate R&D staff in the application of various standards and technologies. Key Core Competencies Requires a detail-oriented self-starter with excellent organizational, planning, and follow-up skills, as well as communication, teamwork, and interpersonal skills. Ability to meet tight competing deadlines, juggle multiple priorities and multi-task. Extensive knowledge of regulatory submission publishing standards and procedures. Education and Experience High School (Bachelor’s degree preferred). Minimum 8 years (w/o Master’s) or 6 – 8 years (with Master’s) years of relevant experience in biotech or pharmaceutical industry. The base salary range for this role is $126,600 to $155,000. Base salary is part of our total rewards package which also includes merit-based salary increases and eligibility for our 401(k) plan, medical, dental, vision, life and disability insurances. Compliance : Achieve and maintain compliance with all applicable regulatory, legal and operational rules and procedures. Mental/Physical Requirements : Fast-paced environment handling multiple demands. Requires a high level of initiative and independence. Sumitomo Pharma America (SMPA) is an Equal Employment Opportunity (EEO) and Affirmative Action employer. #J-18808-Ljbffr
