Support capital project CQV delivery and individual technical contribution solutions for clients within the Life Sciences industry
Job Summary
Support capital project CQV delivery and individual technical contribution solutions for clients within the Life Sciences industry.
Assist in design phases by embedding compliance, testability, and lifecycle thinking, and establish User Requirement Specifications for critical equipment.
Lead client relationship development, project execution, and manage project resources, budgets, and schedules throughout the complete project lifecycle.
Matching Summary
Support capital project CQV delivery and individual technical contribution solutions for clients within the Life Sciences industry.
Skills & Requirements
Must-have
CQV delivery
validation and FDA compliance
commissioning and qualification documents
FAT, SAT, IQ, and OQ documentation
client relationship development
project lifecycle management
Nice-to-have
Truly Human Leadership culture
digital validation tools
progressive digital validation tools
Key Requirements
2-7 years project experience (Validation Engineer II)
7+ years experience (Sr. Validation Engineer)
10+ years experience (Sr. Project Manager)
4+ years computer system validation experience (CSV Engineer)
Bachelor's degree in Engineering
Must be legally authorized to work in the United States without sponsorship
Work Rights
Must be legally authorized to work in the United States without sponsorship