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RA Associate

Zeiss Group
Zeiss Group Salary
Dublin, OH Full Time
POSTED ON 3/7/2025
AVAILABLE BEFORE 6/2/2025
  • Perform the following functions under general supervision :
  • Support pre-market and post-market activities
  • Assist in creation, compilation, and management of regulatory submissions
  • Obtain document notarization, apostillization, legalization, as needed
  • Serve as point of contact for International Affiliates and dealers regarding registration activities
  • Responsible for archiving and maintaining regulatory documents
  • Escalate issues and questions, as needed
  • Train and adhere to regulatory processes Perform other tasks, as assigned
  • Bachelor's degree; degree in a scientific discipline a plus
  • Two years of work experience. Experience in a regulated industry orexperience in regulatory affairs (medical devices) a plus
  • Experience in a fast-paced, multi-tasking, customer-facing environment with deadlines that required strong attention-to-detail and positive outcomes
  • Experience encountering ambiguous situations and determining when to escalate to management
  • Strong verbal and written communication and interpersonal skills
  • Strong time management and organizational skills
  • Strong computer skills including MS Office
  • Knowledge of US, EU and international medical device regulations a plus
  • Certified Notary a plus

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