Highlights:• Possess insightful knowledge of experimental designs, troubleshooting instruments and method development, validation, product release, characterization and stability testing • Expertise in managing larger research projects and investigations in the field of drug development and planning • Exposure in setting specifications and justification of specifications for drug substances and drug products • Proficient in interpreting the results of research projects and recommending new projects or services & rendering advice on research and development options available to the organization • Well versed in handling all kind of dosage forms like Solid orals (Immidiate release/Extended release/sustained release/Oral disintegration tables), Capsules, Suspension, Liposomes, Dermal / transdermal, Emulsions, Depotheraphy, Ophthalmic and injectables • Expert in developing and identifying the right methods for revese engineering of Pharma products (Q1 and Q2 matching) • Good in developing the analytical methods by QBD approach

Skills:Pharmaceutical chemist,Analytical chemist,Scientis

Goal:To became a Successful Analytical Research Scinetist

Certification:Master of Pharmacy in Pharmaceutical chemistry

Honor:• Received Certificate of Excellence for outstanding contribution in development of sustained release dosage form of Milrinone • Received Certificate of Excellence towards technical capabilities, hard work, dedication and team work in completing the development and validation of impurity method for one of the critical projects, • Received Certificate of Excellence for successful delivery of a technically challenging 3- way combination drug product. • Received Certificate of Excellence for towards meticulous thinking, planning and execution of development and GMP manufacturing of 3 combo project

Analytical leas 08/2015 - current
INM Technologies (A shilpa medicare company), Bangalore, karnataka India
Industry: Pharmaceutical
Pharmaceutical formulation analytical development
• Possess insightful knowledge of experimental designs, troubleshooting instruments and method development, validation, product release, characterization and stability testing • Expertise in managing larger research projects and investigations in the field of drug development and planning • Exposure in setting specifications and justification of specifications for drug substances and drug products • Proficient in interpreting the results of research projects and recommending new projects or services & rendering advice on research and development options available to the organization • Well versed in handling all kind of dosage forms like Solid orals (Immidiate release/Extended release/sustained release/Oral disintegration tables), Capsules, Suspension, Liposomes, Dermal / transdermal, Emulsions, Depotheraphy, Ophthalmic and injectables • Expert in developing and identifying the right methods for revese engineering of Pharma products (Q1 and Q2 matching) • Good in developing the analytical methods by QBD approach--
Research Scientist 03/2010 - 07/2015
Syngene intl pvt ltd (A Biocon company), Bangalore, karnataka India
Industry: Pharmaceutical formulation and API (CRO)
Analytical method development for DS and DP
• Planning, organizing, directing, and controlling analytical R&D activities; monitoring research activities through reporting system and advising change as necessary Developing process for therapeutic • Monitoring the method transfer, transition from R&D to QC and GMP/GLP compliance • Preparing documents & maintaining related databases for experiments by following all SOPs worked under stringent GLP guidelines • Collaborating with other research and development departments and providing support in testing of new drug candidates at various stages of development • Implementing systems, migrating systems to upgraded versions to achieve maximum efficiency in various operation; spearheading process improvement initiatives • Maintaining and peer-review documentation such as development report, validation protocol, SOPs, Stability reports, analytical results, laboratory notebooks, electronic data collection / storage software, instrument logbooks and training records • Performing test method transfers, analysis of equilibrium solubility, intrinsic dissolution, 5 stage dissolution, analysis of Dissolution comparison (F2 Comparison) and analysis for solution state stability for pH dependent soluble drugs • Performing analysis of assay, RS, multi media Dissolution, Residual solvent analysis, particle size analysis, content uniformity, assay / RS by GC methods, preformulation activities and physiochemical characterization of drug substances. • Collecting and analysing data using qualitative and quantitative techniques and write up results • Providing training and mentoring new hires and junior analysts • Ensuring adherence to the various quality measures by maintenance of appropriate requisite documentation/ records • Reviewing SOPs, general test procedures, analytical documents & their summary reports • Conducting in-house material testing/ inspection of components • Develop collaboration with external partners and support the internal teams and active participation in innovative research projects as analytical scientist. • Ensure all experiments and functions performed with in the laboratory adhere to the prescribed safety standards, methods and protocols. • Participation in internal audit (as auditor and audited party)--

Rajiv Gandhi University Sciences 04/2004 - 04/2006
Bangalore, karnataka, India
Degree: Master's Degree
Major:Pharmaceutical chemistry
Completed the Master in Pharmaceutical chemistry holding a university Rank

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