At Kailera, we are seeking an Associate Director, Analytical Development and Quality Control to support analytical development and Quality Control operations for clinical development and commercialization of Kailera's pipeline compounds.
Requirements
- 10+ years of experience, or 5+ with advanced degree, in the pharmaceutical/biotech industry
- Strong expertise in analytical techniques HPLC/UPLC, LC–MS, SE-HPLC, dissolution, along with extractables and leachable analysis
- Knowledge of drug development activities with respect to cGMP, quality systems, ICH guidelines, global regulatory requirements, and USP, EP, JP, and CHP requirements
Benefits
- Comprehensive health benefits and tax-advantaged savings accounts
- Flexible time off, 13 paid holidays, and a companywide year-end shutdown
- Monthly wellness stipend
- Generous 401(k) match
- Disability and life insurance