Palvella Therapeutics seeks an Associate Director of Quality Assurance to lead the QMS development, maintenance, and continuous improvement for clinical-stage programs toward potential commercialization.
The role oversees document control, deviation and CAPA management, audits, regulatory compliance, and product release support, while collaborating with Clinical Operations, Regulatory Affairs, CMC, and CMOs to maintain inspection readiness and NDA submission readiness.
#J-18808-LjbffrSenior QA Leader - GMP/GCP, NDA Readiness in pa at Unknown Company
This position is listed as full time and onsite.