Expert Project Engineering & Capital Project Management

From conceptual design through CQV and continuous improvement — we deliver with precision, compliance, and care.

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  • 8+ years experience
  • cGMP & GxP expertise
  • On-site & remote
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Our Services

Supporting pharma, biotech, and advanced manufacturing clients across the full capital project lifecycle.

  • Project Engineering & Owner Representation
  • Capital Project Lifecycle Management (Concept → CQV)
  • Conceptual & Front-End Design Support
  • Construction Administration & Oversight
  • CQV (Commissioning, Qualification & Validation) Execution
  • Change Management & Risk Mitigation
  • Process Optimization & Tech Transfer
  • Facility Expansion & Master Planning
  • Regulatory & GMP Compliance Readiness
  • Continuous Improvement & Post-Project Support

About Us

Jones Consultants is a specialized consulting partner focused on project engineering and capital project execution for the pharmaceutical, biotech, and advanced manufacturing industries. We guide projects from early concept through design, construction, CQV, and ongoing optimization, ensuring that every investment delivers lasting value.

What Makes Us Different

  • Trusted Partner: Acting as an extension of your team, we protect the owner’s interests and ensure that compliance, quality, and performance remain the priority.
  • Project Expertise with Agility: We bring capital project experience and can adapt to meet your needs.
  • Lifecycle Project Management: From conceptual planning to change management and project execution, CQV, and GMP-ready handover, Jones Consultants can deliver experience.
  • Operational Insight: With hands-on GMP operations experience, we design and execute projects that minimize disruption to business-critical activities.

Frequently Asked Questions

We specialize in pharma, biotech, and advanced manufacturing.
Yes, we offer both on-site and remote consulting options.
Yes. We can serve as the owner’s representative to safeguard project goals, budgets, timelines, and regulatory compliance.
We can provide value at any stage—from early site planning and design through CQV execution and post-project continuous improvement. Early engagement maximizes efficiency and risk reduction.
Absolutely. Our team has experience with both targeted facility upgrades and major site-wide expansion projects.
By leveraging GMP operations knowledge, careful scheduling, and change management practices, we execute projects that align with production needs and minimize downtime.

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