Facilitate interface meetings, workshops, and stakeholder reviews, driving timely resolution of interface issues and tracking action items through closure.
Establish and maintain the project interface register, ensuring all interface risks, dependencies, constraints, and decisions are accurately documented and communicated.
Coordinate with EPC contractors, technology licensors, client representatives, and third-party stakeholders to manage cross-organizational interfaces and mitigate execution risks.
Support schedule integration by identifying interface-driven critical path activities, monitoring milestones, and working with project controls teams to resolve potential impacts to project delivery.
Coordinate external interfaces with regulatory agencies, utilities, local authorities, and inspection organizations to ensure alignment with project milestones and readiness objectives.
Lead management of interfaces between project delivery teams and operational readiness, manufacturing, quality, validation, and startup organizations.
Develop and maintain digital interface management systems and reporting tools to improve visibility, accountability, and closure performance.
Ensure all interface management activities comply with project governance requirements, GMP standards, quality systems, regulatory expectations, and company procedures applicable to pharmaceutical facilities.
Prepare and present interface management reports, KPIs, risk assessments, and executive-level updates to project leadership, providing clear visibility of interface performance, emerging risks, and mitigation strategies.
Required Education, Experience, & Skills
Bachelor’s degree in Engineering or project management.
Minimum 15 years of industry experience.
Minimum 10 years of project/program experience supporting pharmaceutical, biotechnology, vaccine, sterile manufacturing, API, or advanced therapy facilities.
Experience on capital project exceeding $500MM TIC.
Experience successfully managing the interface and communications for large multidisciplinary teams and contractors.
Strong knowledge of communications, governance, project controls, design management, and project delivery processes.
Preferred Education, Experience, & Skills
Experience supporting pharmaceutical, biotechnology, or other GMP-regulated facilities.
Prior experience in an Owner’s Representative or PMC role for major capital projects in excess of $1B TIC.
PE, PMP, and/or ISPE certification.
PMC/Owner Representative experience, successful FDA inspection support, and/or greenfield pharmaceutical project experience.
Decarbonization – Energy Transition – Sustainability
KBR Benefits
KBR offers a selection of competitive lifestyle benefits which could include 401K plan with company match, medical, dental, vision, life insurance, AD&D, flexible spending account, disability, paid time off, or flexible work schedule. We support career advancement through professional training and development.
Click here to learn more: KBR Benefits
Belong, Connect and Grow at KBR
At KBR, we are passionate about our people and our Zero Harm culture. These inform all that we do and are at the heart of our commitment to, and ongoing journey toward being a People First company. That commitment is central to our team of team’s philosophy and fosters an environment where everyone can Belong, Connect and Grow. We Deliver – Together.
KBR is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, disability, sex, sexual orientation, gender identity or expression, age, national origin, veteran status, genetic information, union status and/or beliefs, or any other characteristic protected by federal, state, or local law.
