What are the responsibilities and job description for the Ra associate position at Zeiss Group?
- 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 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
Last updated : 2024-10-28
