Site Quality Events Lead for Agilent

Join BIOVECTRA, a part of Agilent, as a Site Quality Events Lead, where you'll spearhead critical investigations in the manufacturing sector. This role demands strong expertise in CAPA and quality management.
As a Site Quality Events Lead, you will drive compliance, facilitate investigations, and work to improve manufacturing operations at the Windsor facility. With over six years of experience in GMP environments, you will collaborate across departments while ensuring diligent adherence to regulatory requirements. This role contributes significantly to enhancing patient care through compliant and effective manufacturing practices.
Key Responsibilities:
• Lead incident investigations in Manufacturing and QC
• Ensure adherence to CGMP, ICH, and Health Canada standards
• Improve deviation and CAPA processes
• Establish investigation workflows and RCA capabilities
• Serve as the primary representative during audits
Requirements:
• Degree in Science or Engineerin...