Experience in pharmaceutical/biopharmaceutical industry. Experience in cGMP environment, including commissioning, qualification and validation.
Well-developed communication skills, both verbal and written.
Demonstrated experience managing teams consisting of internal staff, supervising engineering and construction activities, and preparing turnover documentation from C execution and as-built drawings.
Demonstrated project controls skills such as estimating, scheduling and cost reporting.
Proficient with Microsoft Office products (Excel, Word, PowerPoint, etc.)
Education:
BS in chemical or mechanical engineering, or related degree supplemented with relevant experience.