Sneha Kadam
Garwood,NJ
Summary
Dynamic Scientist III with extensive experience at Eurofins PSS, specializing in analytical characterization of biologics and chromatography techniques. Proven ability to ensure data integrity and compliance with cGMP standards. Skilled in identifying discrepancies and promoting collaboration across teams to achieve successful product development outcomes.
Overview
6
6
years of professional experience
Work History
Scientist III - Group Leader
Eurofins PSS
Branchburg Township, New Jersey
07.2023 - 03.2026
- Performed analytical characterization of biologics, including monoclonal antibodies using HPLC and CE methods.
- Executed chromatography methods, including SEC, RP-HPLC, and IEX for protein purity and identity assessment.
- Supported routine bioanalytical testing for process development and stability studies.
- Analyzed and documented experimental data in compliance with cGMP/GLP and good documentation practices.
- Coordinated sample tracking, storage, and preparation for multiple analytical studies.
- Evaluated laboratory data for compliance with analytical SOPs and GMP requirements.
- Reviewed sample results to ensure accuracy and completeness for reliable data reporting.
- Identified discrepancies, facilitating efficient communication with lab teams to resolve issues.
Chemist
Odin Pharmaceuticals
Somerset, New Jersey
03.2021 - 07.2023
- Conducted qualitative and quantitative analysis of pharmaceutical compounds.
- Developed and validated analytical methods for drug testing and formulation.
- Operated advanced chromatography and spectroscopy instruments for research projects.
- Reviewed analytical data and batch records to ensure GMP compliance
- Verified results against SOPs and specifications to maintain quality standards
- Assisted in implementing corrective actions to resolve compliance issues
- Collaborated with cross-functional teams to ensure compliance with regulatory standards.
- Managed laboratory inventory and maintained accurate documentation of experiments.
- Reviewed technical data and contributed to preparation of scientific reports and presentations.
Analytical Chemist
Leading Pharma
Middlesex, New Jersey
07.2020 - 03.2021
- Developed and validated analytical methods for drug formulations.
- Conducted chemical analyses using HPLC and GC techniques.
- Reviewed lab data to ensure accuracy and compliance with regulatory standards
- Facilitated audit readiness by preparing documentation and coordinating with relevant teams
- Collaborated with cross-functional teams to drive successful product development initiatives
Education
Master's Degree - Biotechnology
Kean University
Union, NJ05-2020
Master of Science - Biotechnology
SRTM University
India06-2015
Skills
- GMP data review
- Data integrity assurance
- Discrepancy identification
- Documentation review
- Chromatography techniques: HPLC, UPLC, SEC, ion exchange (IEX, AEX, CEX), reverse phase
- Protein analysis: ELISA (HCP, protein A), potency assays, monoclonal antibody characterization
- Electrophoretic methods: CE-SDS, CIEF
- Software proficiency: Empower, ELN, Microsoft Office (Excel, Word, PowerPoint)
- Regulatory compliance: cGMP, GLP, GDP
Timeline
Scientist III - Group Leader
Eurofins PSS
07.2023 - 03.2026
Chemist
Odin Pharmaceuticals
03.2021 - 07.2023
Analytical Chemist
Leading Pharma
07.2020 - 03.2021
Master's Degree - Biotechnology
Kean University
Master of Science - Biotechnology
SRTM University