Vega Shetty Email & Phone Number

Cambridge, Massachusetts, US

Cambridge, Massachusetts, US

Cambridge, Massachusetts, US

Cambridge, Massachusetts, US

 Support planning and execution of IVT synthesis and purification development activities appropriate for GMP manufacturing. Conduct, troubleshoot, and modify experiments to reach desired goals of mRNA process development by working closely with Internal Manufacturing.  Provide analytical and bio-analytical characterization of in-house manufactured.

Wilmington, NC, US

 Routinely performed analysis of In-process and release API by analytical techniques such as HPLC, GC and ICP-MS. Successfully executed development of analytical methods and improvement of existing methods to support API development and manufacturing. Drafted and executed validation protocols for analytical methods and independently performed and.

Boston, MA, US

• Researched and developed a thorough understanding of the scope of continuous unit operations by reading relevant literature.
• Successfully developed a high degree of competence in the use of plug flow reactors (PFR), continuous stirred tank reactors (CSTR), mixed suspension mixed product removal reactors (MSMPR), micro-reactors and associated.
• Performed organic synthesis reactions using different types of homemade flow chemistry reactors and also carried out continuous crystallization of organic compounds.
• Routinely conducted the analysis of experiments using analytical techniques like HPLC, GC, and 1 H-NMR and analyzed data to interpret the experimental outcomes.
• Supported the team in developing continuous chemistry processes on specific projects for Vertex.
• Recorded experiments and results in Electronic laboratory notebooks in sufficient detail and documented all the learnings in a systemic manner.

• Actively participated in managing drug product development projects at CMO/CRO’s) to successfully support technical transfer and paediatric development goals.
• Successfully supported commercial readiness and site expansion plans for Auryxia®
• Diligently worked on standardization of knowledge management with CMO using SharePoint and google platforms.
• Supported buid-out of commercial trending program for Auryxia® to include in-process, release and stability data.
• Successfully compiled manufacturing process data for annual reports and other regulatory filing on routine basis
• Routinely supported on-site development activities at CMO’s.

Pittsburgh, PA, US

Research Assistant:1. Determined the thermodynamic transition temperature and other factors which cause polymorphic transformation in crystals and their salts. 2. Set up crystallization of polymorphs and salts of small molecule APIs. Monitored physical stability/time of recrystallization under varied storage conditions.3. Manufactured amorphous solid.

Karachi, Sindh, PK

1. Experienced the organization and working of a clinical pharmacy2. Assisted Clinical Pharmacist in dispensing drugs, counseling patients and contacting health care3. Worked in the Central Sterile Supply Department department and learned to operate in sterile environments. 4. Assisted in managing and organizing inventory.

Master'S Degree, Pharmaceutical Sciences

Pharmaceutical Sciences

Bachelor Of Pharmacy (B.Pharm.), Pharmacy

High School, Hsc: Pcb

High School, Ssc