Primary Responsibilities Include:

• Develops conceptual plans and budgets for facilities projects to support fiscal decision-making.
• Coordinates with proponent groups and committees to facilitate facility planning, budgeting, and scheduling.
• Develops planning documents for initiation of projects to gain approval at Sarepta.
• Prepares requests for proposals and conducts all necessary meetings to facilitate hiring architectural and construction management services.
• Monitors and reports on all phases of planning and construction.
• Coordinates projects with facilities, EHS, Information Technology, and other users to facilitate the installation of equipment, inventory, and other items.
• Coordinates all parties involved in the planning, design, and construction process.
• Develops and maintains facility project budgets.
• Prepares contract change orders and monitors their execution.
• Monitors construction contract close-out and maintains documentation files.
• Coordinates with facility occupants move-in to new facilities.
• Assists in development of new standards of practice for Project Management activities with the Sarepta system.
• Provides subject matter expertise for Mechanical, HVAC, Utilities, and other engineering disciplines as necessary.
• Interfaces with all levels of management in designing and delivering new facilities and modifying existing facilities.
• Works with large A&E and Construction firms to deliver new office, lab, and production facilities.
• Complete other projects and duties as assigned.

Desired Education and Skills:

• B.S./M.S. in Mechanical Engineering.
• 8-10 years of relevant experience in the Pharma/Biotech industry as project manager in a cGMP manufacturing environment.
• Proven ability to work in a cross-functional, fast paced environment and lead multiple capital projects.
• Ability to collaborate cross-functionally and maintain strong working relationships with internal and external collaborators.
• Understanding of all HVAC and utility systems and ability to work with outside contractors.
• Familiar with cGMP regulations and principles, and how to apply them to the development and manufacturing of pharmaceutical/biotech products.
• Excellent communication skills and ability to negotiate and reconcile differences.
• Knowledge of facilities planning and construction management processes and procedures; including interpreting plans and specifications and to compare them with construction progress.
• General knowledge of work order, purchasing, and administrative processes.
• Strong analytical skills; ability to perform detailed analysis of data and information and make recommendations.
• Candidate must be able to travel nationally for up to 30% of the time.

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This position requires work on site at one of Sarepta's facilities in the United States.

Candidates must be authorized to work in the U.S.

Sarepta Therapeutics offers a competitive compensation and benefit package.

Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify.