Bioconjugate Area Lead
- Location
- Richmond, VA · On-site
- Job type
- Full-time
- Level
- Executive
- Experience
- 15+ years
- Education
- Bachelor's degree
- Listed
- 20 days ago
Skills & highlights for this role
- Professional Engineer license
- GMP-regulated facility engineering
- commissioning and qualification (C&Q)
- construction assurance
- operational readiness
- stakeholder management
Also useful
- PMP certification
Stated benefits & perks
- Health
- Dental
- Vision
- 401k match
- Life insurance
About the role
Title: Bioconjugate Area Lead KBR Sustainable Technology Solutions (STS) provides holistic and value-added solutions across the entire asset life cycle. These include world-class licensed process technologies, differentiated advisory services, deep technical domain expertise, energy transition solutions, high-end design capabilities, and smart solutions to optimize planned and operating assets.
KBR is seeking an experienced Bioconjugate Area Lead to serve as the PMC organization's primary owner-representative for the planning, design integration, construction assurance, commissioning, qualification, operational readiness, and startup of the Bioconjugate Manufacturing Area for the client.
Key Responsibilities
Coordinate activities across the client's stakeholders, the PMC team, EPCM contractor(s), equipment suppliers, C&Q teams, and future manufacturing operations to ensure the facility, process systems, utilities, and equipment are delivered safely, compliantly, and in alignment with project cost, schedule, quality, and operational objectives.
Provide leadership in technical decision-making, facility and equipment integration, operational readiness planning, risk management, issue resolution, and stakeholder coordination while ensuring manufacturing, quality, maintenance, and regulatory requirements are incorporated throughout project execution.
Act as the primary integration point for the bioconjugate manufacturing scope Drive cross-functional collaboration from design through startup and Support the successful transition of the facility into routine GMP operations. Required Education & Experience Qualifications Bachelor's degree in Engineering or a related technical discipline.
Minimum 15 years of engineering experience, supporting pharmaceutical, biotechnology, or other GMP-regulated facilities Experience successfully managing large multidisciplinary engineering teams and engineering contractors. Experience supporting commissioning, startup, and operational readiness activities. Demonstrated ability to lead technical decision-making and stakeholder alignment.
Strong leadership and stakeholder management capabilities.
Preferred Qualifications
- Prior experience in an Owner's Representative or PMC role for major capital projects in excess of $1B TIC.
- Professional Engineer (PE) license and/or PMP certification.
- 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.
From KBR's careers page, first listed on Rolev.ai on October 21, 2026. Rolev.ai is not the employer.
How Rolev.ai helps with this application
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Common questions
Where is the Bioconjugate Area Lead job at KBR located?
This Bioconjugate Area Lead position at KBR is located in Richmond, VA (On-site). Always check KBR's application page for specific state eligibility or relocation policies.
What qualifications are required for Bioconjugate Area Lead at KBR?
For the Bioconjugate Area Lead role, KBR highlights 15+ years of relevant experience; a bachelor's degree; experience with GMP-regulated facility engineering, commissioning and qualification (C&Q), construction assurance, operational readiness, stakeholder management. Rolev.ai can score your existing resume against these requirements and show any skill gaps before you apply.
How do I apply for the Bioconjugate Area Lead position at KBR?
This listing links directly to KBR's Workday application page. You can apply directly on KBR's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Workday application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.