Company Description
Meril is dedicated to designing, manufacturing, and distributing top-notch medical devices to alleviate human suffering and enhance quality of life. The company prioritizes research and development, as well as upholding the highest quality standards in Manufacturing, Scientific Communication, and Distribution. Established in 2006 as part of a healthcare diversification plan by a prominent Indian multinational company, Meril is committed to excellence and innovation.
Role Description
This is a full-time Executive role based in Vapi, involving day-to-day responsibilities related to strategic Document Planning. Both GMP and GDP rely heavily on accurate, thorough documentation for compliance with regulations and audits. Understanding regulatory guidelines (e.g., FDA, EMA, WHO) and being familiar with industry standards such as ISO 13485 for medical devices or ISO 9001 for quality management.
Qualifications