Job Details

Senior Specialist, Quality Systems

Our biotech partner is a well-established, commercially successful clinical stage biotech in the Bay Area that is seeking a Senior Specialist of Quality Systems to lead on administration of their Quality Management System and LMS to ensure compliance and operational efficiency. This role requires cross-functional collaboration with the entire team to ensure seamless system operation. The organization is working across a large clinical pipeline of oncology, endocrinology, and metabolic disease programs. This role will require 3 days onsite out of Redwood City, CA.

Responsibilities:

• Administer Veeva QMS & QualityDocs and ComplianceWire LMS
• Manage workflows, user access, and system performance
• Support quality events (deviations, CAPA, change control)
• Lead system optimization and compliance reporting

Requirements:

• 6+ years in pharmaceutical quality systems
• Strong hands-on Veeva and ComplianceWire expertise
• Configuration & lifecycle management experience
• BA/BS in science, tech, or engineering

Contact:

To have a confidential discussion, please contact Amit at ...@meetlifesciences.com and apply to this job posting.