Summary
Overview
Work History
Education
Skills
Accomplishments
Languages
Certification
Timeline
Languages
Personal Information
Publications
Training
Instrumentation Skills
Degree
Languages
Personal Information
Publications
Training
Instrumentation Skills
Generic
Dr Srinivas JAGARLAPUDI CEO-Pharma &LIFE SCINCES EXECUTIVE

Dr Srinivas JAGARLAPUDI CEO-Pharma &LIFE SCINCES EXECUTIVE

Secundrabad

Summary

Dynamic CEO with a proven track record at Visin Labs LLP, excelling in strategic leadership and contract negotiation. Expert in business development and regulatory compliance, foster stakeholder engagement to drive growth and innovation. Successfully negotiated profitable contracts, enhancing organizational performance and establishing a strong corporate identity.

Overview

19
19
years of professional experience
1
1
Certificate

Work History

CEO&Director

Visin Labs LLP
Hyderabad
08.2025 - Current
  • Led strategic initiatives to guide organizational direction and decision-making.
  • Negotiating and closing profitable contracts in accordance with the business plan and agreed margin / cost / volume targets.
  • Developed and aligned technical plan, business plan, and market strategy.
  • Coordinated management team to enhance leadership effectiveness and operational efficiency.
  • Developing existing and building new relationships with relevant Local Authority and professional bodies.
  • Promoted corporate image of Visin Labs LLP through relationships with referrers and businesses, establishing a strong corporate identity.
  • Created meeting agendas and identified key issues for board decisions. Delivered board meeting minutes in a timely manner.
  • To facilitate the establishment and development of training and education at all levels for all staff, in the light of growth of Visin Labs LLP.

CEO& Director

Obvez Labs Pvt Ltd
Hyderabad
01.2018 - 08.2025
  • Negotiated and closed contracts to meet business plan targets for margin, cost, and volume.
  • Guided strategic initiatives to enhance overall business performance.
  • Developed and agreed technical plan, business plan, and market strategy to align with organizational goals.
  • Facilitated leadership among managers to improve team collaboration.
  • Developing existing and building new relationships with relevant Local Authority and professional bodies.
  • Facilitated establishment and development of training and education programs for all staff to support growth of Obvez labs pvt ltd.
  • To promote the corporate image of Obvez labs pvt ltd through interpersonal relations with referrers and businesses, and the establishment of a corporate identity.
  • To ensure that at all times Obvez labs pvt ltd staff, clients and its Board comply with all laws related to its activities and operations.

DGM

Teena Labs
Hyderabad
07.2017 - 02.2018
  • Led technical department to ensure timely task completion within budget and compliance with GMP/regulatory requirements.
  • Planned, supervised, and monitored project activities to achieve milestones within stipulated timelines.
  • Provided regulatory support for Dossier/DMF submissions to European Agencies and US-FDA.
  • Performed inspections for internal, external, and regulatory agencies.
  • Conducted various internal and external audits.
  • Monitored facility adherence to quality systems and GMP.
  • Analytical method development, validation and tech transfer.

Manager

Megsan Labs
Hyderabad
07.2016 - 01.2017
  • Led technical department to ensure timely task completion within budget while adhering to GMP and regulatory requirements.
  • Planned, supervised, and monitored project activities to successfully achieve milestones within stipulated timelines.
  • Handled and reviewed facility compliance with quality systems and GMP standards.
  • Performed inspections for internal, external, and regulatory agencies.
  • Performed a range of internal and external audits.
  • Assisted with Dossier and DMF submissions to European agencies and the US-FDA.
  • Analytical method development, validation and tech transfer.

Manager

Celon Laboratories
Hyderabad
01.2015 - 06.2016
  • Prepared comprehensive Product Development Plan to guide project execution.
  • Designed and performed stability studies in compliance with ICH guidelines to ensure product reliability.
  • Product characterization, design and perform formulation strategies.
  • Scaled up research and development trial batches in preparation for production.
  • Conducted Exhibit Batches (Upscale batches) in Production.
  • Analytical Method Development, Analytical Method Validation, Impurity isolation and characterization.
  • Technology transfer at plant location.
  • Review of specification and method of analysis, method validation report and method transfer report.
  • Investigated incidents and OOS during validation and stability studies, implementing proposed CAPAs to enhance process integrity.
  • Expertise in developing related substances methods for multi combination of drug products.
  • Conducting literature survey, patent search, PIL and review.

Deputy Manager

Wintac Pharma Limited
06.2014 - 11.2014
  • Established new analytical facilities in compliance with current GMP norms, supporting project development and quality assurance.
  • Optimized equipment usage and workforce allocation, enhancing operational efficiency and budget management.
  • Executed Good Laboratory Practices, ensuring regulatory compliance and data integrity.
  • Planned and performed stability studies following ICH guidelines.
  • Effective monitoring of Pre-formulation studies.
  • Preparation & Review of method validation report and method transfer report.
  • Conduct literature search for the analytical methods & degradation pathways and perform method Development for Identification, Dissolution, Assay, Related substances and Residue tests.
  • Reviewing of drug master file.
  • Hands on Solid phase extractions, liquid-liquid extractions, derivatization technique.

Deputy Manager

Aizant Drug Research India
01.2014 - 05.2014
  • Hands on Solid phase extractions, liquid-liquid extractions, derivatization techniques.
  • Highly experienced in handling of Regulatory and Customer audits.
  • Planned and performed stability studies following ICH guidelines.
  • Reviewing of drug master file.
  • Executed the implementation of Good Laboratory Practices (GLP) to ensure compliance with regulatory standards.
  • Utilized equipment, manpower, and budget to optimize laboratory operations.
  • Setting of new Analytical facilities as per current GMP norms.
  • Conducted literature search for analytical methods and degradation pathways, developed methods for identification, dissolution, assay, related substances, and residue tests.
  • Prepared and reviewed specifications and methods of analysis to ensure compliance with regulatory standards.
  • Preparation & Review of method validation report and method transfer report.

Deputy Manager

Hospira
08.2010 - 12.2013
  • Familiar with guidelines like ICH, FDA, EMA, PQRI and OSHA.
  • Expert in Analytical Method Development, Analytical Method Validation, Impurity isolation and characterization for formulation and API.
  • Skilled in Method development and validation for dissolution, Content uniformity, Blend uniformity for solid orals.
  • Expertise in developing assay and related substances methods for multi combination of drug products.
  • In-depth knowledge in determination, method development and validation of elemental impurities as per ICH Q3 (D), USP 232 & 233.
  • Planned leachable and extractable studies for drug products and packaging materials.
  • Rich experienced in developing methods for residue analysis.
  • Demonstrated proficiency in analytical method development and validation, and impurity isolation and characterization using LC-MS and GC-MS to enhance product quality.
  • Planned and executed reverse engineering of innovator products to optimize formulations and improve efficacy.
  • Supervised review of technical documents including method development, validation, technical protocols, reports, MFR, PDR, and stability study protocols to ensure compliance and accuracy.
  • Supervising the review of method transfer activities from R&D to plant to meet timelines.
  • Approved cGMP documents to maintain compliance with regulations.
  • Supervision of equipment qualification (IQ/OQ/PQ) of equipments.

Research Associate

Gland Pharmaceuticals
11.2007 - 08.2010
  • Developed and optimized analytical HPLC, LC-MS, and IC chromatographic methods to enhance accuracy and reliability of results.
  • Isolation of impurities using preparative & semi preparative HPLC.
  • Characterization of impurities, standards and raw materials using spectral techniques like UV, NMR, IR, MS, Elemental analysis, DSC, TGA.
  • Prepared structural elucidation reports for standards, impurities, raw materials, and finished products to ensure compliance and quality.
  • Analysis of Raw materials, finished products and In process-checks.
  • Preparation of method development Protocols, development reports.
  • Coordinated internal audits to assess compliance and identify areas for improvement within the laboratory.

Education

PhD - Chemistry

Sri Krishna Devaraya University
Andhra Pradesh
01-2007

Master of Science - Chemistry

Dr. BAMU University
Hyderabad
01-2002

Skills

  • Strategic leadership
  • Business development
  • Financial acumen
  • Project management
  • Contract negotiation
  • Regulatory compliance
  • Stakeholder engagement
  • scientific Knowledge
  • Quality Management

Accomplishments

  • Skillfully led and managed various formulation development and analytical projects, including research and development projects, for timely completion while designing and developing R&D and manufacturing facilities from ground zero to full operations, including CapEx, OpEx, utilities, etc.
  • Designed technical packages that include prototype formula development, PDR/MFC, pre-formulation studies, technology transfer, stability studies, impurity profiling, reference product characterization, and characterization for drug substances and drug products.
  • Designed, executed, and approved extractable and leachable studies for packing materials and drug products.
  • Certified as an internal auditor by NABL.
  • As a Lead, successfully handled USFDA audits.
  • Designed, executed, and approved nitrosoamines studies for packing materials and drug products.

Languages

English
Proficient (C2)
C2
Telugu
Proficient (C2)
C2
Hindi
Proficient (C2)
C2

Certification

  • CERTIFIED INTERNAL AUDITOR BY NABL
  • Completed training on separation by chromatography
  • Certified independent auditor by IICA

Timeline

CEO&Director

Visin Labs LLP
08.2025 - Current

CEO& Director

Obvez Labs Pvt Ltd
01.2018 - 08.2025

DGM

Teena Labs
07.2017 - 02.2018

Manager

Megsan Labs
07.2016 - 01.2017

Manager

Celon Laboratories
01.2015 - 06.2016

Deputy Manager

Wintac Pharma Limited
06.2014 - 11.2014

Deputy Manager

Aizant Drug Research India
01.2014 - 05.2014

Deputy Manager

Hospira
08.2010 - 12.2013

Research Associate

Gland Pharmaceuticals
11.2007 - 08.2010

PhD - Chemistry

Sri Krishna Devaraya University

Master of Science - Chemistry

Dr. BAMU University

Languages

  • Hindi
  • Telugu
  • English
  • Hindi
  • Telugu

Personal Information

Date of Birth: 06/15/78

Publications

  • J. Srinivas, M. Srinivas, Tathagata Dutta
  • ‘Novel Stability indicating RP-HPLC Method for the Determination of Assay of Voriconazole in Pharmaceutical Products’. Saudi J. Med. Pharm. Sci.; Vol-1, Iss-3(Nov, 2015):70-79.
  • J. Srinivas, V.S. N. Rao et.,al.,.” Non Extractive simultaneous Spectrophotometric determination of trace quantities of Pd(II) and W(VI).Analytical letters, 44:5,815-823,2011.
  • J. Srinivas, Pape Gowd C.T, Rao Surayanarayana V.” Spectrophotometric determination of trace amounts of palladium in alloys”. Research Journal of Chemistry environment India. Vol: 12(1) mar 2008.
  • B. Venkata Narayana, J. Srinivas, V.S. N. Rao” Spectrophotometric determination of trace amounts of molybdenum in alloys”. Research Journal of Chemistry environment India. Vol: 10 (3) Sep 2006.
  • Dr. J. Srinivas et.,al., “Second Order Derivative Spectro-photometry for Simultaneous determination of Pd(II) and W(VI) Using 3,4 Di-hydroxy benzaldehyde isonicotinoyl hydrazone (DHBINH)”. International Journal of Chemical and Physical Science. 2019, 7(3): 64–66.
  • Dr. J. Srinivas et.,al., “Simultaneous determination of Mo (VI) and W(VI) using Second order Derivative Spectro-photometry”. International Journal Current trends and Pharmaceutical Research”. 2018, 6(6): 114-116.
  • Dr. J. Srinivas et.,al., “Novel Stability indicating RP-HPLC method for the determination of Ondansetron Impurities in Ondansetron Injection”. International Journal Current trends and Pharmaceutical Research. 2018, 6(4): 103-109.
  • Dr. J. Srinivas et.,al., RP-HPLC Stability indicating method for Separation Impurities In Voriconazole”. International Journal of Research in Pharmacy and Life Sciences. 2018, 6(1): 25–30.
  • Dr. J. Srinivas et.,al., “Formulation and Evaluation of Lamivudine Extended release Tables” Asian Journal Medical and Pharmaceutical Sciences. 2018, 6(2): 66-74.
  • Dr. J. Srinivas et.,al., Development of Formulation and Evaluation of Stavudine extended Release Tablets” . Journal of Pharmaceutical and Biological Research, 2018, 6(I): 11-19.
  • Dr. J. Srinivas et.,al., Analytical Method Development for the Estimation of Related Substances by high Performance Liquid Chromatography Rimonabent (RIM) drug”. Asian Journal of Clinical Research.
  • Dr. J. Srinivas et al., “Fermentation Studies on α- Galactosidase production”. World Journal Pharmacy and Biotechnology.
  • Dr. J. Srinivas et al., “Second Order derivative Spectro-photometry for Simultaneous determination of Hg(II) and Ti(IV) Using 3,4 Di-hydroxy benzaldehyde Isonicotinoyl hydrazone (DHBNH)”. International Journal Current trends and Pharmaceutical Research.
  • Dr. J. Srinivas et al., “Simultaneous determination of RU (II) and W(VI) using Second order Derivative Spectro-photometry”. International Journal of Medicine and Pharmaceutical Research.
  • Dr. J. Srinivas et al., “A New non –extractive Spectro-photometric method for the determination of trace Quantities of Titanium (IV)”. Journal of pharmaceutical and Biomedical Analysis Letters.

Training

  • Attended seminars organized by Separation science in Singapore on method development & validation.
  • Advanced HPLC method development training by John .W.Dolan in Chennai.
  • Attended seminars conducted by various vendors / suppliers & institutional trainers.
  • Deftly underwent onsite 5 day (class room / field / Mock drill etc,) training programme on basic fire safety, and first aid conducted by Usha Fire systems at Hyderabad.

Instrumentation Skills

  • HPLCs (Waters, Agilent, Shimadzu) Detectors: UV, RI, ELSD, FLR, CORONA.
  • UPLC (Ultra performance Liquid Chromatography) waters, shimadzu.
  • LC-MS (Agilent, waters, Thermo).
  • Preparative HPLC (Auto purification MS).
  • GC-MS (Perkin Elmer, Shimadzu).
  • Gas chromatography-Detectors FID, TCD (Agilent, Shimadzu, Perkin).
  • Ion-Exchange chromatography (Metrohm, Thermo).
  • Dissolution Apparatus- Type-I, Type-II and Type-IV.
  • ICP-MS (Agilent).
  • ICP-OES (Agilent).
  • Particle size analyzer (Malvern) 3000.
  • Panda.
  • High pressure homogenizer.

Degree

  • M.SC
  • Ph.D.

Languages

  • Hindi
  • Telugu
  • English
  • Hindi
  • Telugu

Personal Information

Date of Birth: 06/15/78

Publications

  • J. Srinivas, M. Srinivas, Tathagata Dutta
  • ‘Novel Stability indicating RP-HPLC Method for the Determination of Assay of Voriconazole in Pharmaceutical Products’. Saudi J. Med. Pharm. Sci.; Vol-1, Iss-3(Nov, 2015):70-79.
  • J. Srinivas, V.S. N. Rao et.,al.,.” Non Extractive simultaneous Spectrophotometric determination of trace quantities of Pd(II) and W(VI).Analytical letters, 44:5,815-823,2011.
  • J. Srinivas, Pape Gowd C.T, Rao Surayanarayana V.” Spectrophotometric determination of trace amounts of palladium in alloys”. Research Journal of Chemistry environment India. Vol: 12(1) mar 2008.
  • B. Venkata Narayana, J. Srinivas, V.S. N. Rao” Spectrophotometric determination of trace amounts of molybdenum in alloys”. Research Journal of Chemistry environment India. Vol: 10 (3) Sep 2006.
  • Dr. J. Srinivas et.,al., “Second Order Derivative Spectro-photometry for Simultaneous determination of Pd(II) and W(VI) Using 3,4 Di-hydroxy benzaldehyde isonicotinoyl hydrazone (DHBINH)”. International Journal of Chemical and Physical Science. 2019, 7(3): 64–66.
  • Dr. J. Srinivas et.,al., “Simultaneous determination of Mo (VI) and W(VI) using Second order Derivative Spectro-photometry”. International Journal Current trends and Pharmaceutical Research”. 2018, 6(6): 114-116.
  • Dr. J. Srinivas et.,al., “Novel Stability indicating RP-HPLC method for the determination of Ondansetron Impurities in Ondansetron Injection”. International Journal Current trends and Pharmaceutical Research. 2018, 6(4): 103-109.
  • Dr. J. Srinivas et.,al., RP-HPLC Stability indicating method for Separation Impurities In Voriconazole”. International Journal of Research in Pharmacy and Life Sciences. 2018, 6(1): 25–30.
  • Dr. J. Srinivas et.,al., “Formulation and Evaluation of Lamivudine Extended release Tables” Asian Journal Medical and Pharmaceutical Sciences. 2018, 6(2): 66-74.
  • Dr. J. Srinivas et.,al., Development of Formulation and Evaluation of Stavudine extended Release Tablets” . Journal of Pharmaceutical and Biological Research, 2018, 6(I): 11-19.
  • Dr. J. Srinivas et.,al., Analytical Method Development for the Estimation of Related Substances by high Performance Liquid Chromatography Rimonabent (RIM) drug”. Asian Journal of Clinical Research.
  • Dr. J. Srinivas et al., “Fermentation Studies on α- Galactosidase production”. World Journal Pharmacy and Biotechnology.
  • Dr. J. Srinivas et al., “Second Order derivative Spectro-photometry for Simultaneous determination of Hg(II) and Ti(IV) Using 3,4 Di-hydroxy benzaldehyde Isonicotinoyl hydrazone (DHBNH)”. International Journal Current trends and Pharmaceutical Research.
  • Dr. J. Srinivas et al., “Simultaneous determination of RU (II) and W(VI) using Second order Derivative Spectro-photometry”. International Journal of Medicine and Pharmaceutical Research.
  • Dr. J. Srinivas et al., “A New non –extractive Spectro-photometric method for the determination of trace Quantities of Titanium (IV)”. Journal of pharmaceutical and Biomedical Analysis Letters.

Training

  • Attended seminars organized by Separation science in Singapore on method development & validation.
  • Advanced HPLC method development training by John .W.Dolan in Chennai.
  • Attended seminars conducted by various vendors / suppliers & institutional trainers.
  • Deftly underwent onsite 5 day (class room / field / Mock drill etc,) training programme on basic fire safety, and first aid conducted by Usha Fire systems at Hyderabad.

Instrumentation Skills

  • HPLCs (Waters, Agilent, Shimadzu) Detectors: UV, RI, ELSD, FLR, CORONA.
  • UPLC (Ultra performance Liquid Chromatography) waters, shimadzu.
  • LC-MS (Agilent, waters, Thermo).
  • Preparative HPLC (Auto purification MS).
  • GC-MS (Perkin Elmer, Shimadzu).
  • Gas chromatography-Detectors FID, TCD (Agilent, Shimadzu, Perkin).
  • Ion-Exchange chromatography (Metrohm, Thermo).
  • Dissolution Apparatus- Type-I, Type-II and Type-IV.
  • ICP-MS (Agilent).
  • ICP-OES (Agilent).
  • Particle size analyzer (Malvern) 3000.
  • Panda.
  • High pressure homogenizer.
Dr Srinivas JAGARLAPUDI CEO-Pharma &LIFE SCINCES EXECUTIVE