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Senior Regulatory Affairs Specialist Job Locations US-OH-Cincinnati Company Meridian Bioscience, Inc. Department Quality & Regulatory Affairs

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1 About Meridian Meridian Bioscience is a fully integrated life science company that develops, manufactures, markets and distributes a broad range of innovative diagnostic products. We are dedicated to developing and delivering better solutions that give answers with speed, accuracy and simplicity that are redefining the possibilities of life from discovery to diagnosis. We are looking for talented and passionate individuals that help drive our vision. Our innovative culture will allow interested candidates to discover and create, through collaboration, cutting edge solutions to tough problems. Job Summary Responsible for supporting Meridian's regulatory and quality processes, including Meridian's product realization process, to ensure that Meridian's activities are consistent with applicable quality and regulatory requirements, especially the design, development and manufacture of medical devices. Assist the regulatory department with product compliance throughout all stages of the product lifecycle, including research, development, transfer, validation/verification, labeling, regulatory submissions, and lifecycle maintenance. Works cross-functionally to ensure that regulatory guidance is provided in support of business objectives. Key Duties Tasks/Duties/Responsibilities: Provides support and guidance to quality and regulatory activities, including Design Control activities, project teams, design transfer activities, clinical trials, validation and verification activities, and existing product modifications. Supports and helps draft sections of regulatory submissions for domestic, world-wide commercialization and other business objectives. Drafts, evaluates, and reviews technical protocols and data in support of clinical trials, validation, verification and product manufacturing. Provides direct support associated with adverse events, medical device reportable events and product recall activities, including corrections and removals. Evaluates the regulatory impact of changes associated with product design change and routine change control. Drafts and reviews, and helps provide guidance for product labeling activities, including Instructions for Use (IFU/PI), to ensure adherence to applicable regulations and standards. Provides regulatory input and oversight to product lifecycle planning, including risk management activities, and monitors product lifecycle and compiles information associated with changes as directed. Compiles new product technical information and feature summaries in support of market expansion. Responds to Sales & Marketing requests to ensure content of collateral and promotional materials is compliant with applicable regulations. Participates in long-term projects supporting the business and quality objectives of the organization. Assists in the management of third party and internal Quality Audit programs; perform supplier audit and verification activities as directed. Other duties as assigned: Physical Must be able to adhere to applicable bio-safety practices when on the manufacturing floor or in laboratories. Ability to sit for long periods, stoop, reach and bend throughout the course of the work shift. Ability to work on a PC including repetitive use of a keyboard and mouse for long periods throughout the course of the workday. Other Ability to concentrate, problem solve and review paperwork for extended periods of time. Ability to analyze and interpret data. Qualifications Minimum Education or Equivalent Experience Required/Preferred: Bachelor of Science degree i