Regulatory Affairs Professional
2 days ago
o Supports worldwide product registrations by providing information and documents to Siemens Regional Unit (RU) in Asia-Pacific, Middle East Asia, South and Latin America and Europe.
- o Provides answers to technical questions from Siemens Regional Unit (RU) and international regulatory authorities.
- o Prepares and/or compiles technical documents for the global dossier and country specific requirements.
- o Supports projects related to new country and new product registrations, as well as license renewals, and re-registrations due to product changes.
- o Liaises with Regulatory Affairs (RA) core team, design change team, and international RA members to support product registrations worldwide.
- o May have various interdepartmental communications with marketing, manufacturing, R&D, Original Equipment Manufacturers (OEM) labeling, and others to support an efficient and effective international product registration process.
**Organization**: Siemens Healthineers
**Company**: Siemens Healthineers India LLP
**Experience Level**: Experienced Professional
**Full / Part time**: Full-time
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