Ramesh A. Email & Phone Number

Hyderabad, In

Hyderabad, Telangana, India

Mentoring and Manage to provide technical leadership to the R&D team in generic formulation development, and monitor quality of execution. Coordinate with cross functional teams for alignment to deliver quality product on timelines and budget.

Bucharest, Romania

Manage the formulation development work of solid oral dosage forms for Europe market from strategy, feasibility studies, submission batches and to interpret study results. Support the product validation and launch efforts of the developed products and answer deficiency questions from regulatory authorities. Investigate issues with existing products or manufacturing processes with an intent to either resolve the issue or improve the product quality.

Ahmedabad, Gujarat, India

Manage a team for Formulation development of generic pharmaceutical dosage forms for regulated markets of US, Europe and to guide the subordinates to ensure smooth technology demo to tech transfer team.

Hyderabad, Telangana, India

To manage and guide subordinates for end-to-end formulation development of oral solid dosage forms for US regulated market from inception up to pilot batch manufacturing, followed by regulatory queries and support for validation batches.

Hyderabad, Telangana, India

Manage a team of Formulation Development Scientists and technicians / operators, taking responsibility for manpower recruitment, resource planning, staff development and prioritization of formulation development of generic dosage forms for regulatory submission of Europe, Turkey and US markets.

Istanbul, Turkey

Development of various pharmaceutical dosage forms for regulatory submission of Europe market. Independent performance of pre formulation studies, designing of formulation plans/strategies, execution of experiments, prototype declaration, optimization of trials, and document preparedness for technology transfer activities. Undertaking scale up batches, exhibit batches, writing protocols, SOPs, and product development reports

Hyderabad, India

Development of various pharmaceutical dosage forms (Immediate release/modified release tablets, coated pellets for delayed release and lyophilized parenteral products) for regulatory submission of US and Europe markets. Independent performance of pre formulation studies, designing of formulation plans/strategies, execution of experiments, prototype declaration, optimization of trials, and document preparedness for technology transfer activities. Undertaking scale up batches, exhibit batches, writing protocols, SOPs, product development reports and answering post submission regulatory queries..

Hyderabad, India

1) Pre-clinical formulation development of New chemical entities (NCEs) for pharmacokinetic, bioavailability and toxicokinetic studies and further involves bioavailability and solubility enhencement by various techinques involving cyclodextris, solid dispersions, micronisation, polymorpsim, salts, microemulsions etc. 2) Preformulation studies involving physico-chemical characterisation of NCEs including solubility, hygroscopicity, compatability, solid state stability, solution state stability, solid state manipulation, salt screening and dissolution development. 3) Further, dosage form development including injections, tablets, capsules for technology transfer for clinical dosage form development.

M. Pharmacy, Pharmaceutics

Activities and Societies: 1) Secured 19 th rank in all india entrance conducted by MAHE (Manipal Academy of Higher Education).

B. Pharmacy