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881 jobs found
06.04.2024
3M
3M Regulatory Affairs Specialist United States, Oregon
Lead/coordinate medical device and cosmetic regulatory affairs for part of the US designed portfolio. Coordinate communication and compliance globally. Support international requests. Support new product introductions and existing product changes....
Support the development of domestic and international strategies for regulatory approval of Class I, II and III medical devices. Represent RA on cross functional projects which may include product development,...
Lead/coordinate regulatory operations systems and master data support; organizational subject matter expert. Lead connection with IT to represent regulatory needs for systems as required; represent design requirements for system. Provide...
The Manager is responsible for supporting the Regulatory Affairs strategic vision and regulatory leadership in defining the global regulatory strategy for biosimilar projects. The Manager is accountable to support the...
Publish and dispatch major and complex routine/lifecycle management eCTD submission projects. Perform document level publishing activities, troubleshoot document issues and perform quality control checks for submission ready documents. Collaborate with...
Manage resources to support submission activities for responsible sites and oversees the coordination and delivery of major submissions to directly support the companies growth strategy. Build relationships with RA staff/authoring...
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...
Lead/coordinate medical device and cosmetic regulatory affairs for part of the US designed portfolio. Coordinate communication and compliance globally. Support international requests. Support new product introductions and existing product changes....
Are you looking for a way to make a difference in the tech industry? Consider a rewarding and challenging career as a regulatory affairs specialist! These professionals play an essential role in getting new technologies approved and accepted into the marketplace.
The primary responsibility of a regulatory affairs specialist is to ensure that proposed products and services comply with applicable standards, regulations and guidelines. This may involve researching existing regulations, working on technical documents, and coordinating with regulatory bodies during the submission and review process. Regulatory affairs specialists must have a thorough understanding of relevant regulatory authorities and relevant industrial regulations.
Regulatory affairs specialists must demonstrate excellent attention to detail, problem-solving and communication skills, in addition to excellent technical knowledge. The ability to interpret large amounts of technical data and write clear reports and documents is essential. Regulatory affairs specialist must be comfortable working independently and collaboratively in fast-paced and dynamic environments.
At Expoint, you'll find numerous opportunities for regulatory affairs specialists, ranging from entry-level positions to managerial roles. As a regulatory affairs specialist, you'll gain valuable experience and insight into the tech industry, all while working with motivated colleagues and discovering new, cutting-edge technologies. If you're detail-oriented, have great communication skills and an interest in the tech industry, consider a career as a regulatory affairs specialist.