Project Manager - Clayton NC
NNE · Clayton, NC · 5 days ago
On-siteInformation Technology$20/hrFull-time
About the job
Lead the future of pharma engineering as a Project Manager at NNE in Clayton—where you’ll drive high-impact projects, manage cross-disciplinary teams, and deliver real results for global drug production. If you’re ready to innovate, collaborate, and make a difference in a dynamic environment, this is your opportunity to shine. Join us and turn your talent into meaningful progress.
Primary Duties and Responsibilities
- Define the strategic and tactical framework for projects and lead execution of design through construction and hand over to deliver objectives within scope, schedule, budget, and quality requirements.
- Lead cross-disciplinary teams by establishing clear direction, responsibilities, and priorities, while ensuring the resources and support needed for predictable project execution are in place.
- Build and maintain effective relationships with customers, project teams, contractors, and senior stakeholders through proactive communication, alignment, and issue resolution.
- Proactively identify, manage, and mitigate project risks, issues, and changes to protect project objectives and business outcomes.
- Drive continuous improvement and identify opportunities to enhance customer value, efficiency, and project performance.
Required Qualifications
- Willingness and ability to be based in Clayton, working in an agile, fast-paced, project-oriented environment that supports both customers and colleagues.
- Thrive in dynamic settings, bringing energy, structure, and empathy to every project.
- A natural communicator who builds trust quickly and leads with curiosity, confidence, and clarity.
- Passionate about solving complex problems and inspiring teams to achieve excellence.
- Continuously expand capabilities through learning, feedback, and reflection.
- Bachelor’s or Master’s degree in Engineering or a related technical discipline.
- Minimum 5 years of project management experience, including at least 3 years in the pharmaceutical industry.
- Proven success managing mid-to-large scale design projects with total installed cost (TIC) ranging from $20M to $300M.
- Strong familiarity with GMP, project lifecycle methodologies, and design documentation standards.
- PMP certification or equivalent is a plus.