Sanofi medical regulatory writer job openings in Hyderabad for all Lifesciences candidates having experience in medical wring.
Sanofi is a global pharmaceutical company with a presence in Hyderabad, India. The company has several facilities in the city, including research and development centers, manufacturing sites, and offices. Sanofi’s presence in Hyderabad allows it to tap into the talented pool of scientific and medical professionals in India, as well as to serve the growing healthcare needs of the local population.
job description for medical regulatory writers;
- A medical regulatory writer is a professional who specializes in writing and preparing regulatory documents for the pharmaceutical and medical device industries.
- Their main responsibilities include creating and reviewing documents such as investigational new drug applications (INDs), new drug applications (NDAs), and pre-market approval (PMA) submissions to the FDA.
- They must have a strong understanding of regulatory requirements and guidelines, as well as knowledge of the medical and scientific terminology used in the industry.
- Medical regulatory writers work closely with teams of scientists, physicians, and regulatory affairs specialists to ensure that the documents they prepare accurately reflect the safety and efficacy data of a product. Their work plays a crucial role in the approval and marketing of new medical treatments and devices.
The role of a medical regulatory writer at Sanofi is critical to the success of the company’s product development and marketing efforts. By working to ensure that regulatory submissions are accurate and complete, they help to ensure that Sanofi’s products can be brought to market as quickly and efficiently as possible.
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