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    "name": "SURYA SAI HARSHA  KARRA",
    "summary": "Experienced Regulatory Affairs Associate with expertise in FSSAI compliance and regulatory submissions. Successfully led end-to-end regulatory compliance for a weight management supplement, ensuring adherence to guidelines and maintaining meticulous documentation throughout the product lifecycle. Dedicated to optimizing regulatory processes and collaborating with cross-functional teams to enhance product approval outcomes. Recognized for strong technical writing skills and a methodical approach to documentation control. Actively seeking opportunities in Regulatory Affairs where I can apply my regulatory expertise and contribute to compliant product development and successful submissions.",
    "location": "Hillsboro, Portland",
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        "network": "LinkedIn",
        "username": "surya-sai-harsha-karra-064a97191",
        "url": "https://linkedin.com/in/surya-sai-harsha-karra-064a97191"
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  "work": [
    {
      "company": "Lactonova Nutripharm Pvt. Ltd.",
      "position": "Regulatory Affairs Associate & Product Management Trainee",
      "location": "Hyderabad, India",
      "startDate": "2023",
      "endDate": "2025",
      "highlights": [
        "Facilitated comprehensive regulatory compliance and product lifecycle management for gummies, capsules, protein powders, softgels, and dietary supplements, ensuring accurate nutritional label review and ingredient verification",
        "Executed in-depth scientific literature, regulatory, market, and competitor analyses to drive product development and ensure compliance with industry standards",
        "Coordinated with R&D, QA, Manufacturing, and Marketing teams to align regulatory requirements with compliant product development and successful launches",
        "Developed and scrutinized technical documentation, product brochures, presentations, and promotional materials to meet regulatory and product management standards",
        "Harvested and analyzed import/export market data using Volza to enhance market research and inform product strategy"
      ]
    }
  ],
  "education": [
    {
      "institution": "St. Joseph College for Women",
      "degree": "Master of Science",
      "field": "Organic Chemistry",
      "startDate": "2021",
      "endDate": "2023",
      "score": "7"
    },
    {
      "institution": "Centurion University of Technology & Management",
      "degree": "Bachelor of Science",
      "field": "Chemistry",
      "startDate": "2017",
      "endDate": "2020",
      "score": "8.2"
    }
  ],
  "skills": [
    "FSSAI Compliance",
    "Regulatory Submissions",
    "Product Lifecycle Management",
    "Regulatory Documentation Control",
    "Cross-functional Collaboration",
    "Costing Analysis",
    "Global Supplier Engagement",
    "Ingredient Specification Review",
    "Documentation Control",
    "Formulation Understanding",
    "Dosage Form Costing (Tablets / Capsules / Soft gels / Gummies)",
    "MS Excel",
    "MS Word",
    "PowerPoint",
    "Volza",
    "Adobe",
    "Regulatory Strategy",
    "Team Leadership",
    "Communication Skills"
  ],
  "languages": [
    {
      "language": "English",
      "fluency": "Fluent"
    },
    {
      "language": "Hindi",
      "fluency": "Fluent"
    },
    {
      "language": "Odia",
      "fluency": "Fluent"
    },
    {
      "language": "Telugu",
      "fluency": "Native"
    }
  ],
  "projects": [
    {
      "name": "Silica Aerogel",
      "description": "Conducted a research project on the synthesis, properties, and potential pharmaceutical applications of silica aerogel. The project focused on understanding its lightweight, porous structure and evaluating its potential applications in areas such as insulation and drug delivery."
    },
    {
      "name": "Diazo Coupling Reaction for the Synthesis of Azo Dyes",
      "description": "Conducted a research project on the synthesis of azo dyes using diazo coupling reactions. The project involved performing the reaction, studying the properties of the synthesized products, and documenting experimental procedures and laboratory findings."
    }
  ],
  "certificates": [
    {
      "name": "FRA: Global Regulatory Strategy for Pharmaceuticals",
      "issuer": "RAPS",
      "date": "2026-08",
      "url": "https://learningportal.raps.org/base/certificate/PDFCertificate?id=01302CC81E86492E81F7E751D3E971ED&userId=D2CBC5F83532401FA52821ADB0373291&contentId=B7B059F762C74737BFE047A3D245F6B0&attemptId=153E141B15064DD7BA9FBE8C48A487B7&creditTypeId=&cd=inline"
    },
    {
      "name": "Human Subjects Research (HHS/OHRP) Certification",
      "issuer": "HHS/OHRP",
      "date": "2026-07"
    },
    {
      "name": "Health Insurance Portability and Accountability Act (HIPAA) Certification",
      "issuer": "HIPAA",
      "date": "2026-07"
    },
    {
      "name": "Certificate Course in Drug Regulatory Affairs",
      "issuer": "Udemy",
      "date": "2026-08"
    },
    {
      "name": "Professional Certificate Course in Drug Regulatory Affairs",
      "issuer": "Udemy",
      "date": "2026-08"
    },
    {
      "name": "Good Clinical Practice Certification",
      "issuer": "GCP",
      "date": "2026-08"
    },
    {
      "name": "Master Pharma Regulatory Affairs: FDA, EMA & Global Regulations",
      "issuer": "Udemy",
      "date": "2026-08"
    },
    {
      "name": "eTMF Management & Clinical Trial Documentation Masterclass",
      "issuer": "Udemy",
      "date": "2026-08"
    }
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      "Lactonova Nutripharm Pvt. Ltd.",
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      "Chemistry",
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      "Regulatory Submissions",
      "Product Lifecycle Management",
      "Regulatory Documentation Control",
      "Cross-functional Collaboration",
      "Costing Analysis",
      "Global Supplier Engagement",
      "Ingredient Specification Review",
      "Documentation Control",
      "Formulation Understanding",
      "MS Excel",
      "MS Word",
      "PowerPoint",
      "Volza",
      "Adobe",
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      "Team Leadership",
      "Communication Skills",
      "FRA: Global Regulatory Strategy for Pharmaceuticals",
      "Human Subjects Research (HHS/OHRP) Certification",
      "Certificate Course in Drug Regulatory Affairs",
      "Professional Certificate Course in Drug Regulatory Affairs",
      "Good Clinical Practice Certification",
      "eTMF Management & Clinical Trial Documentation Masterclass",
      "English",
      "Hindi",
      "Odia",
      "Telugu"
    ],
    "yearsOfExperience": 4,
    "seniority": "junior",
    "highestEducation": "Master's"
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