Analytical Documentation officer

minimum of 5 years of experience in pharmaceutical analytical R&D or QC comes under this category.

Understating Good Laboratory Practices and Good Document Practices.

Should have exposure in electronic DMS systems.

Preparation and upload of Standard operating procedures, Spec and MOA in DMS.

Notifying pharmacopeia updates to the analytical team and preparing the assessment report.

The analytical team at R&D is playing an important role in product development of various dosage forms. The analytical team involves different workflows like analytical method development, stability studies, involving method verifications at CMO/CTL and post filling activities.

This role is with Azurity R&D Analytical Review team, which coordinates all product development team’s analytical documents preparation such as SOP, COA, ATP, Specification and Method of analysis.