Offer summary
Qualifications:
PhD in analytical chemistry with 3+ years’ experience or BS/MS with 5+ years’ experience, Experience with regulatory filings desired, Strong background in mass spectrometry and method development, Knowledge in analytical development for small molecules and oligonucleotides, Effective verbal and written communication skills.
Key responsabilities:
- Guide CRO in robust method development and validation
- Develop quality control strategy for drug substances/products
- Manage product stability study programs
- Coordinate with QA, Regulatory, and clinical functions
- Design experiments for characterization of drug materials