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.
Develop and execute validation and FDA compliance related documents/protocols, prepare and execute commissioning and qualification documents, and conduct investigations.
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
troubleshoot validation-related issues
project management and leadership
Nice-to-have
digital validation tools
client relationship development
multiple project responsibilities
people-centric leadership
Key Requirements
Minimum 2-7 years project experience (Validation Engineer II)
Minimum 7+ years experience (Sr. Validation Engineer)
Minimum 10+ years experience (Sr. Project Manager)
Bachelor's degree in Engineering
Proficiency with Microsoft Office, Microsoft Project, AutoCAD
Willing and able to travel
Work Rights
Must be legally authorized to work in the United States