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 in design phases by embedding compliance, testability, and lifecycle thinking, and establish User Requirement Specifications for critical equipment and systems.
Lead all aspects of client relationship development and project execution, including developing project plans, 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 lifecycle management
Nice-to-have
people-centric leadership
digital validation tools
progressive digital validation tools
Key Requirements
2-7 years project experience (Validation Engineer II)
7+ years demonstrated experience (Sr. Validation Engineer)
10+ years project engineering/management experience (Sr. Project Manager)
4 years computer system validation experience (CSV Engineer)
Bachelor's degree in Engineering
Work Rights
Must be legally authorized to work in the United States without sponsorship