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Industrious, Enterprising and Highly accomplished Analytical Lab Manager credited with 12+ years of experience in the field of Pharmaceutical Quality Control and Analytical R&D. Outstanding strategist and creative problem solver distinguished for demonstrated leadership and team building skills and excellent communications abilities.
Areas of Expertise include

  Experience with UV-VIS Spectroscopy, HPLC, UPLC, GC, GC-MS/MS, ICP-MS, FTIR, Dissolution apparatus, Polarimeter, Karl Fischer, TGA, DSC, XPRD and other basic Chemical and Analytical Techniques.
  Experience in Method development, Method Validation and Method Transfer.
  Extensive knowledge of cGMP, Data Integrity and Compliance guidelines provided by FDA.
  Extensive knowledge of regulatory (ICH, FDA, EMA) and compendial guidance and practical experience in meeting requirements in all phases.
  Expertise in analyzing Finished Products, In-Process Samples and Raw Materials and Stability Samples
  Experience in writing and reviewing Analytical Method Validation Protocols and Reports.
  Experienced in resolving OOS or OOT investigations.
  Experienced in Calibration of analytical instruments and routine maintenance.
  Experience in troubleshooting on chromatographic instruments.


Amassed nearly 19 years of progressive experience spanning Analytical Research & Development (R&D), Quality Control (QC) in API and Formulation, and Regulatory Compliance, bringing a unique blend of technical depth, operational leadership, and regulatory expertise. Recognized for driving innovation in analytical sciences, developing, validating, and transferring novel analytical methods for Assay, Impurities, Nitrosamine Impurities, Dissolution, Residual Solvents, and PSD Methods, ensuring regulatory-ready data packages and smooth technology transfers. Hands-on expertise across a suite of advanced techniques: HPLC, UPLC, GC, Dissolution, UV-Vis, FTIR, PSD, LC-MS, HRMS, GC-MS, DSC, and XRD, applying them to resolve challenging scientific, regulatory, and manufacturing problems. Hands-on experience across Solid orals, Liquid orals, Semi-solids, Injectables, Medicinal devices, Female hormones and Active pharmaceuticals. Skilled in end-to-end project ownership, from conceptualizing analytical strategies to executing ANDA submissions, managing site/ technology transfers, conducting comparative dissolution studies, and supporting global regulatory filings (USFDA, EMA, MHRA, HC, TGA, WHO, and other major markets). Strategic thinker with expertise in designing fit-for-purpose analytical systems and compliance frameworks that align GLP, GMP, GDP, 21 CFR Part 11, and data integrity standards, resulting in audit readiness and zero-observation outcomes. Proven ability to translate complex data sets into actionable insights, supporting decisions in drug development, lifecycle management, impurity qualification, risk assessment while safeguarding product quality and patient safety. People-oriented leader with skills in building, mentoring, and scaling high-performing teams of ~60 scientists by introducing structured training programs, competency-building frameworks, and culture of accountability.

Proficient in conducting laboratory and field experiments while informing new hires on research methods and data collection procedures. Hardworking and driven with superior organizational and analytical skills combined with unparalleled dedication to research excellence. Skilled in the conceptualization, design, and implementation of oral solids, liquids, and injectables projects.

Over 14 years of work experience. A highly motivated and result driven professional utilizing enthusiasm, perseverance and strong desire to learn to contribute and make a positive difference to the organization. Seeking a position where acquired knowledge and experience will be utilized with a well-established organization.

Abhinav Pandurang Tambare

Summary

Education

M. Pharm - Pharmaceutics

B.Pharm -

HSC -

SSC -

Skills

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M. Pharm - Pharmaceutics

B.Pharm -

HSC -

SSC -

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