Pharmaceutical Ops & Technology
Executes capital projects ranging from multiple small projects to a large project (>$ 40 million). Duties include engineering management, construction management, budgeting, reporting, scheduling/sequencing, program management and safety.
1) Manages all aspects of a capital project or multiple small projects including budgets, schedule, engineering (Non-process), construction, coordination and safety.
2) Provides support to Denmark manufacturing, facilities and other European site groups via investigations, studies and consulting. Support may extend to other sites as assigned.
3) Manages and monitors the activities of outside engineering, construction managers and contractors working on capital projects.
Knowledge of industry standards and guidelines, such as, ASME BPE, ISPE Baseline Guides and CFR’s.
Prior experience in an engineering, construction, commissioning or validation capacity for capital projects in the biotech/pharmaceutical industry.
Experience in retrofit projects for licensed facilities, previous manufacturing experience in a cGMP environment or previous architectural/engineering firm experience.
Budgeting and scheduling experience.
Experience in equipment, piping, skid or module fabrication in a biotech/pharma-manufacturing environment.
Experience in non-GMP project management – labs, office, utilities, etc.
University Degree: Engineering or related with a typical minimum of 8 years of related industry experience.