Job Description
Role Overview:
As a Bioanalytical Scientist, you will be responsible for providing bioanalytical support to projects in development from pre-clinical studies to clinical stages. You will work in the Research and Development department, performing method development and validation of bioanalytical methods for small molecules in biological fluids using HPLC and LC-MS/MS methodologies in a GLP environment. Your role will involve conducting sample analysis, providing bioanalytical support to clinical and non-clinical studies, and reporting data to line management and pharmacokineticists. Additionally, you will be responsible for drafting bioanalytical study plans and reports, performing data analysis, and participating in general regulated bioanalytical laboratory operations.
Key Responsibilities:
- Perform method development and validation of bioanalytical methods for small molecules in biological fluids using HPLC and LC-MS/MS methodologies in a GLP environment
- Conduct sample analysis and provide bioanalytical support to clinical and non-clinical studies
- Report data to line management, pharmacokineticists, and data management
- Draft bioanalytical study plans and bioanalytical reports for method validation and sample analysis studies
- Perform other bioanalytical work as assigned based on project and Company needs
- Take part in general regulated bioanalytical laboratory operations including maintenance and calibration of equipment, and ordering lab supplies
- Perform required data analysis, review data of moderate complexity, interpret data findings, investigate issues, and report abnormalities
Qualifications Required:
- Ph.D. in Chemistry, Biochemistry, or a related field
- 02-05 years of work experience in a relevant field
- Strong technical expertise in bioanalysis using relevant computer software (Analyst, WinNonlin/Phoenix, etc.) preferred
- Good knowledge of regulatory guidelines/requirements regarding bioanalysis, able to follow & prepare SOPs
- Basic knowledge of DMPK and overall drug discovery and development process is required
Note: The job posting is in Baddi and the recruitment status is in process for a full-time position with an immediate date of joining. Role Overview:
As a Bioanalytical Scientist, you will be responsible for providing bioanalytical support to projects in development from pre-clinical studies to clinical stages. You will work in the Research and Development department, performing method development and validation of bioanalytical methods for small molecules in biological fluids using HPLC and LC-MS/MS methodologies in a GLP environment. Your role will involve conducting sample analysis, providing bioanalytical support to clinical and non-clinical studies, and reporting data to line management and pharmacokineticists. Additionally, you will be responsible for drafting bioanalytical study plans and reports, performing data analysis, and participating in general regulated bioanalytical laboratory operations.
Key Responsibilities:
- Perform method development and validation of bioanalytical methods for small molecules in biological fluids using HPLC and LC-MS/MS methodologies in a GLP environment
- Conduct sample analysis and provide bioanalytical support to clinical and non-clinical studies
- Report data to line management, pharmacokineticists, and data management
- Draft bioanalytical study plans and bioanalytical reports for method validation and sample analysis studies
- Perform other bioanalytical work as assigned based on project and Company needs
- Take part in general regulated bioanalytical laboratory operations including maintenance and calibration of equipment, and ordering lab supplies
- Perform required data analysis, review data of moderate complexity, interpret data findings, investigate issues, and report abnormalities
Qualifications Required:
- Ph.D. in Chemistry, Biochemistry, or a related field
- 02-05 years of work experience in a relevant field
- Strong technical expertise in bioanalysis using relevant computer software (Analyst, WinNonlin/Phoenix, etc.) preferred
- Good knowledge of regulatory guidelines/requirements regarding bioanalysis, able to follow & prepare SOPs
- Basic knowledge of DMPK and overall drug discovery and development process is required
Note: The job posting is in Baddi and the recruitment status is in process for a full-time position with an immediate date of joining.
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