Job Description :-
- Study Design & Management : Designing and executing pre clinical studies (animal models, bench testing) to evaluate performance and safety.
- Regulatory Compliance : Ensuring all studies follow GLP (Good Laboratory Practice) guidelines and generating documentation for FDA or regulatory submissions.
- Data Analysis & Reporting : Analyzing experimental data, interpreting results, and writing technical reports to support regulatory submissions.
- Collaboration : Working with R&D, regulatory affairs, and quality assurance teams.
- Experience : 3 to 5+ years in laboratory settings, with experience in in vivo or in vitro testing.
- A mix of laboratory work, office-based data analysis, and regulatory documentation.
Qualification :- Master's or Ph.D. in Biomedical Engineer
Experience :- 4-5 years
