Role & responsibilities Collaborate with cross-functional teams to gather product information for initiating labeling activities related to new dossiers, query responses, commercial manufacturing updates, or variation sub...

The Regulatory Manager will be responsible for overseeing and ensuring that all food compliance mandates related to FSSAI and AYUSH formulation guidelines are strictly adhered to. This includes managing compliance for Zeons d...

We are seeking a diligent Regulatory Affairs Executive to support our compliance efforts, ensuring adherence to FSSAI, Legal Metrology, and AYUSH regulations. The successful candidate will play a key role in preparing and sub...

Role & responsibilities 1. Preparation and reviewing of CTD and ACTD dossier.2. Co-ordination with Plant and R&D to collect inputs required for Regulatory Submission.3. Co-ordination with plant for Regulatory complian...

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...

Preparation & review of US ANDAs/ 505(b)(2)/EU/ Canada dossiers for Parenteral products as per regulatory requirements. Preparation & review of deficiency responses, regulatory strategy note, controlled correspondence...

To prepare documents Technology Transfer Document, Product scale up report, Product development report, Chemistry manufacturing & control, Polymorphism study etc.To collect necessary information from all concerned Departm...

To prepare documents Technology Transfer Document, Product scale up report, Product development report, Chemistry manufacturing & control, Polymorphism study etc.To collect necessary information from all concerned Departm...

Job Requirement : Deputy Manager - Regulatory Affairs 1) Preparation of dossier from M1 to M5 in eCTD for US/EU/UK/Canada/Austrilia/NewZealand market. 2) Preparation of MoH/Clients query response 3) Preparation of supplem...

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...

Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step be...

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,...

Regulatory Affairs Officer:  A Regulatory Affairs professional ensures a company's products comply with relevant government regulations by managing the process of submitting required documentation to regulatory agenci...