Venu Reddy M

• Working for PharmaBlock since march 1st 2022, as Associate principal scientist in CDMO-Process Research department.
• Responsible for managing process FTE projects for US clients, route scouting, process optimization to support discovery process and GLP and GMP manufacturing.
• Route scouting and Process development of several intermediates and building blocks for leading drug products from lab to to pilot plant scale.
• Leading team of 5 chemists to assist daily work, monitor projects progress and trouble scouting.
• Management of Process FTE projects by communicating with clients, through emails, weekly updates and presentations.
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vWorking for Pharmablock since 13th February 2019, as Assistant Director in
CDMO-Process Research department.
Responsible for managing process FTE projects for US clients, route scouting, process
optimization to support GMP manufacturing.
Leading team of 5 chemists to assist daily work, monitor projects progress and trouble
scouting.
Management of Process FTE projects by communicating with clients, through emails,
weekly updates and presentations.

• Successfully Completed DMF Filling of Valsartan for CFDA, which includes process development & optimization, parameter study, impurity profiling, spiking studies.
• Responsible for product development from grass root level to manufacturing site, dealt with DOE (Orthogonal Experimental Design) to improve the process of the selected route in development stage.
• Responsible for daily work assignments for team (Team size-3 chemists), work proposal and plan, trouble shootings, preparation of Technology Development package (TDP) and Genotoxic impurity (GTI) evaluation reports.
  

• Successfully completed process optimization of API molecules Suvorexant, Dasabuvir and their intermediates.
• Established the simple and efficient purification technique for the critical API,Dasabuvir in final stage with Purity >99.8A%.
• Responsible for daily work assignments for team (Team size- 3 chemists).
• Team discussions, trouble shootings, Data analysis, Process development reports and weekly updates.

• Successfully completed Process Development (Route feasibility & optimization, lab and kilo lab validation of API molecules Darifenacin.HBr.
• Worked on troubleshooting of OOS issues during stability study of Esomeprazole Magnesium Dihydrate and Trihydrate.
• Responsible for preparation of weekly and monthly updates.
• Achieved project objectives by troubleshooting experiments and testing practical and creative solutions. Collaborated with leadership team to identify relevant questions and determine best methods of collection.

• Completed Process Development of API molecules like Deoxycholic Acid from lab scale to kg scale in manufacturing site.
• Process research and scale-up to multi hundred-gram scale of Latanoprost and got appreciation from supervisor.
• Responsible for literature search and analytical data integration.
• Gathered, arranged and corrected research data to create representative graphs & charts highlighting results for presentations.
• Validated incoming data to check information accuracy and integrity while independently locating and correcting concerns.

• Exposed to process optimization of several key API intermediates and custom synthesis molecules.
• Completed several Med chem projects on small scale for customers like Pfizer, Merck, Roche.
• Planned and conducted research experiments in lab during this period.
• Evaluated lab findings to make interpretations and write reports.