Pawan V.

Section Director (Director V) @Texas Department of State Health Services

Austin, TX, US
MOBILE NUMBERS
+91 *********19

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WORK HISTORY

Dec 2025 — Present

Section Director (Director V) @Texas Department of State Health Services

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Austin, TX, US

Medical screening unit operation, technical, and management.

EDUCATION

1994 — 1996

Postgraduate Institute of Medical Education and Research

Master of Science - MS, Biochemistry (Clinical Biochemistry, Molecular Biology and Immunology)

2014 — 2016

Saint Mary's University of Minnesota

Master of Business Administration (MBA), Operational management of Diagnostic/Healthcare facilities and healthcare administration

1997 — 2002

Panjab University

Ph.D. (Doctor of Philosophy), Biochemistry/Biotechnology

SKILLS

CellAnimal ModelsRt-PcrCell SignalingMolecular BiologyCancerImmunohistochemistryPhysiologyCancer ResearchSequencingQpcrVascular BiologyCell BiologyBiochemistryProteomicsCell CultureIn VivoCell Based AssaysPcrTransfectionMicroscopyMicrobiologyImmunologyToxicologyInfectious DiseasesBiotechnologyDrug DiscoveryBusiness DevelopmentBusiness Process ImprovementOperations ManagementHealthcare ManagementProgram ManagementProduct ManagementProduct Lifecycle Management

ABOUT PAWAN V.

As a laboratory operation management leader with technical expertise, I led patient diagnosis, operation management, and design of new diagnostic tests for patient care, provided efficient diagnostic testing utilization, and optimized processes with high-quality results. Planning, budgeting, and managing the operation of the medical screening unit with 5 branch managers. Managing a budget of ~ 150 million service contract. Continuous communication with legislators, nursing staff, hospitals, etc, to provide the best/most compassionate services to newborn babies and Medicaid patient care management. I was involved in business advisory teams and new business proposal analysis for new or rare disease diagnoses. Completed many market surveys to capture the new markets by repositioning the operation focus through budgeting and profit & loss statements analysis. Established technical, scientific, and administrative standards following GLP/GCP/CLIA/CAP compliance and initiated corrective action to improve efficiency. Also provided leadership and consultation on all regulatory standards and patient reporting. Responsible for troubleshooting and addressing issues in the clinical laboratory areas, including LC-MSMS, clinical chemistry testing, and next-generation sequencing strategies. Responsible for reviewing quality control, quality assurance programs, and adjusting policies. Ultimate intent for sustainability, lower cost, higher quality, and techniques to improve efficiency and agency revenue.

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