Scientific Director, Pharmaceutical Development Analytics
US CA San Diego, United States
USD 163K-223K Executive-level Full Time
Tasks
- Build response surface and statistical models
- Design and apply advanced statistical methods
- Develop control strategies linking material attributes process parameters and product performance
- Ensure statistical methods align with ICH guidelines
- Identify critical material attributes and critical process parameters
- Integrate development analytical and manufacturing data
- Lead statistical support for CMC regulatory submissions
- Provide statistical and quantitative leadership for drug product development
- Support process characterization scale up and robustness assessments
Perks/Benefits
- Health insurance
- Medical leave
- Paid Holidays
- Paid caregiver leave
- Paid parental leave
- Paid personal days
- Paid vacation
- Retirement savings plan with company match
Skills/Tech-stack
Blending | Cause analysis | Coating | Compression | Critical Process Parameters | Critical Quality Attributes | Data Visualization | Data integration | Design of Experiments | Design space | Granulation | ICH Q10 | ICH Q14 | ICH Q8 | ICH Q9 | JMP | Multivariate analysis | Process Variability | Process characterization | Process parameters | Process variability analysis | Python | Quality attributes | Quantitative modeling | R | Response surface methodology | Risk Analysis | Root Cause Analysis | Root cause | Solid Oral Dosage | Statistical Analysis | Statistical modeling | Statistics | Variability analysis
Education
Regions
Countries
States
Cities
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