Rachana Mahesh Jadhav

Experienced in the Analytical development and validation of respiratory and OSD formulations, with a strong focus on accuracy and precision. Skilled in handling and calibrating instruments for optimal performance and reliable results. Proficient in analyzing and interpreting data to identify trends and patterns for decision-making. Committed to strict adherence to regulatory guidelines and industry standards, constantly seeking opportunities to enhance processes and improve efficiency. Well-versed in Quality Assurance and Regulatory Affairs basics. Actively seeking an opportunity to leverage expertise in Analytical Development to further professional interests and contribute to the success of your organization.

• Sound knowledge of drug development process and regulatory documentation.
• Good computer skills and knowledge of relevant applications like MS Office (Word/Excel/Power Point), Adobe, Outlook.
• Capacity to multitask and complete assigned responsibilities within stipulated timelines.
• Ability to perform tasks independently as well as effectively and collaboratively within a team.
• Good written and verbal communication and presentation skills.
• Self-motivative.

• Certificate Course in Drug Regulatory Affairs Conducted by SG Pharma training instructor Varsh Kakkar.

• Quality assurance
• Regulatory Affairs