Description:
Exp- 8+ years Strong knowledge of GMP, FDA, ISO standards, and regulatory requirements. Demonstrated project management expertise, preferably PMP or equivalent certification. Excellent leadership, communication, and interpersonal skills. Ability to manage multiple projects in a fast-paced, dynamic environment. Proficiency with manufacturing/ERP software and MS Office Suite. Experience in the Medtech Industry. Cardiovascular device manufacturing experience preferred Six Sigma, Lean Methodo
Aug 25, 2025;
from:
dice.com