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Dyna David

Dyna David

Research and Development

Talent
New DelhiMember since April 15, 2026
Analytical Method Development & Validation (ICH Guidelines)Scientific & Medical WritingGood Laboratory Practices (GLP)HPLCUV-Visible SpectroscopyDissolution ApparatusEmpower SoftwareLabSolutions SoftwareCHEMIA SoftwareAPMS SoftwareLIMSMS Office (Advanced Excel, Word, PowerPoint)Problem-SolvingTime ManagementAttention to DetailCommunication
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Analytical Method Development & Validation (ICH Guidelines)Scientific & Medical WritingGood Laboratory Practices (GLP)HPLCUV-Visible Spectroscopy

About

Detail-oriented MSc.

Analytical

Chemistry professional with 5.5 years of experience in pharmaceutical R&D. Expertise in analytical method development, validation, and regulatory documentation as per ICH guidelines. Strong in data analysis, scientific documentation, and cross-functional collaboration. Interested in literature review, clinical research, and evidence-based healthcare analysis with a strong inclination toward transitioning into research-focused roles.

Experience

Research Associate at Micro Labs Limited (R&D) (2021-07 – 2025-12)

Conducted pharmaceutical R&D activities including analytical method development, validation, and regulatory documentation

  • Prepared and executed validation protocols and reports as per ICH guidelines (Accuracy, Precision, Linearity, Robustness)
  • Developed and validated analytical methods for assay, dissolution, and content uniformity
  • Handled multiple analytical projects with strict regulatory timelines
  • Ensured compliance with US/EU regulatory requirements for submission batches
  • Performed calibration of HPLC, Dissolution, and analytical instruments
  • Generated, analyzed, and trended analytical data using CHEMIA and APMS
  • Prepared documentation for regulatory submissions and validation reports
  • Maintained GLP compliance across all analytical activities
  • Managed stability studies including sample tracking and data monitoring
  • Conducted root cause analysis for analytical deviations (where applicable)
  • Reviewed scientific literature and regulatory guidelines to support development
  • Interpreted data and prepared structured technical reports
  • Collaborated with cross-functional teams for project execution

Research Associate Trainee at Medley Pharmaceuticals (2020-07 – 2021-07)

Supported pharmaceutical R&D activities including analytical testing and method development for oral dosage forms

  • Executed development trial batches for oral dosage forms for regulated markets
  • Operated HPLC, UV-Visible, and Dissolution instruments
  • Performed calibration and routine maintenance of laboratory instruments
  • Prepared reagents, standards, and samples for analysis
  • Reviewed scientific data and literature to support development work
  • Documented experimental procedures and results in structured format
  • Supported preparation of technical and research reports
  • Collaborated with teams to meet project timelines

Education

M.Sc. in Analytical Chemistry – Guru Nanak Khalsa College, Mumbai (2016-01 – 2018-01)

B.Sc. in Chemistry – Mumbai University (2012-01 – 2015-01)

Skills

Research and Development

Reviews