Technical Project Manager

Description

• Providing the client with necessary information and resolving most project issues with the client.
• Direct and review work of project design team; check progress of work and alert managers to change in scope and additional services.
• Coordinate project design with other engineering disciplines.
• Lead the technical engineering efforts and act as the Technical “conscience” for projects.
• Prepare initial budget, tracking overall costs, approving pending invoices, and pursuing change orders as required.
• Manage all phases of a project - setup, execution, and closeout
• Develop and maintain project and resource schedules
• Ensure project deliverables meet TAI and client expectations
• Perform overall project quality control.
• Develop and maintain project management deliverables such as project control and execution plans, risk registers, and regular project progress reports.
• Lead and task manage teams of Subject Matter Experts
• Independently work with code officials and other design professionals when an interpretation or exception to codes is required.
• Research and apply applicable industry codes
• Provide a single point of contact between TAI and client – getting info from client for the design,
• Direct CAD designers for the preparation of construction drawings.
• Define and secure the necessary Subject Matter Experts (SME).

Requirements

• Minimum of ten years of experience reviewing and approving PFD’s, P&ID’s, equipment and piping specifications. Preferably, knowledge preparing documents.
• Great leadership, interpersonal and communication skills
• Minimum of ten years of experience in utilizing construction documents for life sciences/pharmaceutical facilities.
• Basic understanding of all engineering disciplines with capacity to self-perform process engineering.
• Minimum 3 to 5 years’ experience managing life science engineering projects at new or existing facilities.
• Experience with FDA, EMA, and other regulatory standards and requirements required
• Understanding of process controls
• Minimum of ten years of applicable consulting or engineering experience within life sciences/ pharmaceutical industry.
• Advanced knowledge and application of cGMP’s and ASME BPE required
• Microsoft Office applications – Word, Excel, PowerPoint and Project
• Professional Engineer or PMP is a plus
• Ability to work independently and within a team
• Bachelor’s Degree in Engineering (Mechanical or Chemical is preferred) from an accredited university
• Ability to perform field work that will include walking, kneeling, sitting, standing, climbing stairs and/or ladders.
• Must be willing to travel to client sites
• AutoCAD (ability to open drawings, navigate, edit text, and print) - Preferred
• The ability to balance your work and family activities.

Benefits

• PTO and Paid Holidays
• Flexible work schedule
• Professional Development, Tuition Reimbursement, and Association Membership Reimbursements.
• Health Benefits: Employee through family level coverage for medical, dental, and vision insurances. Company funded life and long-term disability insurances. Short Term Disability, FSA, HSA, EAP, and supplemental life insurances (employee – family) are also available!
• Work in a dynamic and collaborative environment that values creativity and innovation.
• Pay: $150,000 – 185,000 annually (based upon experience)
• The opportunity to make a real impact on a variety of industry-leading projects.
• A chance to learn and grow alongside some of the brightest minds in engineering.
• 401(k)with employer match
• Annual Profit Sharing Bonus (variable)

Training + Development

Interview process

Visa Sponsorship

Security clearance