Key Responsibilities: Prepare and compile Drug Master Files (DMFs) for China in compliance with regulatory guidelines. Conduct thorough reviews of technical and regulatory documentation to ensure accuracy and compliance. P...

Client's Company Profile: Our client is into Import & Export of Pharmaceutical / Medical Device Company (European MNC). The company provides tailored intelligent healthcare solutions based on the latest professional insi...

Job Summary Global Calcium is seeking a Manager - Regulatory Affairs with expertise in Drug Master File (DMF) & CEP filings and global regulatory submissions. The ideal candidate will be responsible for preparing, reviewing,...

Your tasks and responsibilities: > You will be closely aligned with the Siemens Healthineers Regulatory team to support required activities for our employees to achieve and maintain legal compliance as a prerequisite for glo...