<ul><li>In the Indian context, an Analytical Documentation professional is responsible for creating and maintaining detailed records of analytical procedures and results within the pharmaceutical or research industry.&nbsp;</li><li>This role involves preparing comprehensive documentation compliant with regulatory standards, including those set by agencies like the Drug Controller General of India (DCGI). Analytical Documentation specialists collaborate closely with quality assurance and regulatory affairs teams to ensure adherence to Indian pharmaceutical regulations.&nbsp;</li><li>Strong attention to detail, knowledge of Good Laboratory Practices (GLP), and familiarity with Indian pharmacopoeial standards are crucial for success in this role. Effective communication skills and the ability to adapt to evolving regulatory requirements are also essential.</li></ul>

Research Associate/Sr. Research Associate-Analytical Documentation