Genpact (NYSE: G) is a global professional services and solutions firm delivering outcomes that shape the future. Our 125,000+ people across 30+ countries are driven by our innate curiosity, entrepreneurial agility, and desir...

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...

Company Description Believe is one of the worlds leading digital music companies. Believes mission is to develop local artists and labels in the digital ecosystem by providing them the solutions they need to grow their audie...

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,...

Job title: Associate Project Manager Medical Affairs Hiring Manager: Team Lead Projects Location: Hyderabad % of travel expected: Travel required as per business need Job type: Permanent and Full time About the job Ou...

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...