Material Handling Automation for Life Sciences
Connecting pharmaceutical facility design, automation and operations to accelerate the path to autonomous production
The future of life sciences manufacturing is shaped by smarter material handling.
Jacobs integrates facility design, robotics, AMRs, cobots and digital systems to automate material movement across life sciences facilities, from feasibility through operations.
What material handling automation enables
Material handling automation reduces repetitive material movement, sampling and routine workflows, allowing teams to focus on the decisions, judgment calls and quality work that deliver therapies to patients faster.
Reduce exposure to repetitive motion and manual material handling risks with autonomous systems designed for the realities of pharmaceutical manufacturing and Good Manufacturing Practice (GMP) production.
Minimize process variation and contamination risk while improving traceability and audit-readiness across every stage of pharmaceutical manufacturing.
Connected systems improve visibility and responsiveness, protecting production continuity as labor shortages and demand for complex therapies grow.
Build flexibility into life sciences facility design, enabling an automation footprint to scale up or down as needs, technology and demand evolve.
Supporting organizations to make capital decisions based on where it's most strategic to build, rather than where labor happens to be available.
Core features
Material handling automation master planning: Assess current-state operations, define automation maturity goals and build a phased roadmap that aligns facility design, workforce strategy and technology investment from day one.
Facility and material flow design: Design corridors, airlocks, cleanroom layouts, major equipment integration and material flow paths that accommodate autonomous mobile robots (AMRs) and automated material handling alongside people in life sciences facility design.
Dynamic material movement simulation: Model AMR routes, throughput and human-robot interactions virtually to de-risk design decisions before construction begins.
Robotics and automation design: Co-create technical specifications, evaluate qualified vendors, and support RFI/RFP development and vendor selection for AMRs, pharmaceutical robotics and cobots.
IT/OT architecture and connectivity: Design resilient wireless infrastructure, network segmentation and cybersecurity strategies that keep connected fleets and systems communicating reliably.
Commissioning, qualification and validation (CQV) support: Guide quality and regulatory teams through the unique validation challenges associated with pharmaceutical manufacturing automation, autonomous and robotic systems in GMP environments.