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  "basics": {
    "name": "Vaishali Patel",
    "summary": "PhD and MPharm-qualified pharmaceutical sciences professional with over 8 years' experience in analytical method development, validation, and pharmaceutical quality assurance. Skilled in HPLC, HPTLC, UV spectroscopy, and regulatory compliance under ICH guidelines. Seeking to leverage strong research and teaching expertise in pharmaceutical analytics to advance quality and innovation.",
    "location": "Vadodara, India",
    "profiles": [
      {
        "network": "LinkedIn",
        "username": "vaishalipharmaceuticals",
        "url": "https://linkedin.com/in/vaishalipharmaceuticals"
      }
    ]
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  "work": [
    {
      "company": "Parul Institute of Pharmacy and Research, Parul University",
      "position": "Professor - Pharmaceutical Sciences, Department of Pharmaceutical Quality Assurance",
      "location": "India",
      "startDate": "2017-11",
      "endDate": "2024-12",
      "highlights": [
        "Delivered lectures and hands-on training in Pharmaceutical Analysis and Quality Assurance for B.Pharm and M.Pharm students",
        "Provided lab training on assay procedures, standardization, and instrumental analysis techniques",
        "Trained students in HPLC, HPTLC, UV-Visible, and IR spectroscopy practicals",
        "Supervised pharmaceutical compound assays including ferric and ferrous ion estimation",
        "Guided sample preparation, method execution, data acquisition, and analytical result interpretation",
        "Ensured compliance with Good Laboratory Practices (GLP) and lab safety standards"
      ]
    },
    {
      "company": "Indubhai Patel College of Pharmacy and Research Center",
      "position": "Assistant Professor - Pharmaceutical Sciences",
      "location": "India",
      "startDate": "2016-09",
      "endDate": "2017-11",
      "highlights": [
        "Delivered theory and practical training in Pharmaceutical Analysis, Quality Assurance, and Instrumental Analysis for B.Pharm and M.Pharm students",
        "Conducted lectures on method development, validation principles, and pharmaceutical analysis concepts",
        "Provided hands-on training in HPLC, HPTLC, UV-Visible and IR spectroscopy",
        "Supervised drug assay, standardization, and analytical lab experiments",
        "Guided student projects on method development, validation, and data interpretation",
        "Ensured compliance with ICH Guidelines and GLP standards"
      ]
    },
    {
      "company": "Cadila Pharmaceuticals",
      "position": "Research Project Trainee (R&D – ADL Department)",
      "location": "Dholka, Gujarat, India",
      "highlights": [
        "Developed a stability-indicating RP-HPLC method for estimating Azilsartan Kemedoxomil in bulk and pharmaceutical dosage forms",
        "Performed method development, optimization, and validation under ICH Guidelines",
        "Evaluated validation parameters including specificity, accuracy, precision, linearity, robustness, and system suitability",
        "Conducted forced degradation studies under acid, base, oxidation, thermal, and photolytic conditions",
        "Prepared analytical reports, validation protocols, and regulatory-compliant documentation",
        "Gained exposure to R&D lab practices, instrumentation handling, and analytical troubleshooting"
      ]
    }
  ],
  "education": [
    {
      "institution": "Parul University",
      "degree": "Doctor of Philosophy (PhD) Pharmaceutical Sciences",
      "endDate": "2025"
    },
    {
      "institution": "Dharmsinh Desai University",
      "degree": "Master of Pharmacy (MPharm) Pharmaceutical Quality Assurance",
      "endDate": "2015"
    },
    {
      "institution": "Rajiv Gandhi Proudyogiki Vishwavidyalaya University",
      "degree": "Bachelor of Pharmacy (BPharm)",
      "endDate": "2012"
    }
  ],
  "skills": [
    "Analytical Method Development",
    "HPLC",
    "HPTLC",
    "UV-Visible Spectroscopy",
    "Pharmaceutical Quality Assurance",
    "ICH Guidelines",
    "Method Validation",
    "GLP Compliance",
    "Regulatory Documentation",
    "Instrument Calibration",
    "Scientific Writing",
    "Dissolution Testing",
    "Stability Studies",
    "Routine Analytical Testing",
    "Pharmacopoeial Standards",
    "GDP",
    "GMP Requirements",
    "Analytical Troubleshooting",
    "Data Analysis",
    "Technical Report Writing",
    "Regulatory-Compliant Documentation",
    "Particle Size Distribution Techniques",
    "Gel Filtration Chromatography",
    "Light Scattering",
    "Diffraction",
    "Obscuration Methods",
    "Assay of Iron Forms",
    "Labile Iron",
    "Chelation Assays",
    "Reduction Potential",
    "Kinetic Studies",
    "Complex Injectable Pharmaceutical Systems",
    "Good Documentation Practices",
    "Preparation and Review of SOPs",
    "Analytical Reports",
    "Quality Documentation",
    "Operation, Calibration, and Routine Maintenance of Analytical Instruments",
    "Analytical Troubleshooting and Root Cause Investigation",
    "Laboratory Quality Systems",
    "Compliance Procedures",
    "Analytical Method Transfer",
    "Technology Transfer Processes",
    "Regulatory Documentation Requirements",
    "Data Integrity",
    "Compliance Expectations in Regulated Environments",
    "Scientific Communication",
    "Behavioral Skills",
    "Analytical Thinking",
    "Problem-Solving Ability",
    "Data Interpretation",
    "Presentation Skills",
    "Effective Communication",
    "Cross-Functional Coordination",
    "Positive Attitude",
    "Adaptability",
    "Strong Documentation Discipline"
  ],
  "languages": [
    {
      "language": "English",
      "fluency": "Fluent"
    }
  ],
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    "sponsorship": false
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      "Analytical Method Development",
      "HPLC",
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      "ICH Guidelines",
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      "Regulatory Documentation",
      "Instrument Calibration",
      "Scientific Writing",
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      "GMP Requirements",
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      "Diffraction",
      "Obscuration Methods",
      "Assay of Iron Forms",
      "Labile Iron",
      "Chelation Assays",
      "Reduction Potential",
      "Kinetic Studies",
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      "Good Documentation Practices",
      "Preparation and Review of SOPs",
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      "Quality Documentation",
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      "Data Integrity",
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      "Scientific Communication",
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      "Presentation Skills",
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      "Positive Attitude",
      "Adaptability",
      "Strong Documentation Discipline",
      "English"
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    "yearsOfExperience": 0,
    "seniority": "entry",
    "highestEducation": "Doctorate"
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