Support both capital project CQV delivery and individual technical contribution solutions for clients within the Life Sciences industry
Job Summary
Support both capital project CQV delivery and individual technical contribution solutions for clients within the Life Sciences industry.
Assist basic and conceptual design phases of capital projects by working with clients and vendors on embedding compliance, testability and lifecycle thinking into early design.
Lead all aspects of client relationship development and project execution, developing project plans, strategies, and managing resources, budgets, and schedules.
Matching Summary
Support both capital project CQV delivery and individual technical contribution solutions for clients within the Life Sciences industry.
Skills & Requirements
Must-have
validation and FDA compliance
commissioning and qualification documents
FAT, SAT, IQ, and OQ documentation
client relationship development
project plans, strategies, budgets, and schedules
Nice-to-have
Truly Human Leadership culture
digital validation tools
entire project lifecycle experience
Key Requirements
2-7 years project experience (Validation Engineer II)
7+ years experience (Sr. Validation Engineer)
10+ years experience (Sr. Project Manager)
Bachelor's degree in Engineering
Must be legally authorized to work in the United States
Work Rights
Must be legally authorized to work in the United States